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The General Introduction of Vector Libraries

Synbio Technologies' vector libraries offer you a one-stop service withextensive vector selection. The libraries contain vectors for various species such as E. coli, yeast, and mammals, catering to your downstream research needs. Existing vectors are readily available for immediate use! Need to modify the vectors? Just edit and synthesize!

We provide an online editing function to make vector modification more efficient, allowing you to edit and customize your desired vectors in real-time. Our efficient synthesis service ensures rapid and accurate delivery of vectors. Synbio Technologies' vector construction platform is a powerful and reliable ally for your scientific research projects!

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Cloning Vectors

• Cloning VectorsView More

Vector Number	Functional Description	Name	Prokaryotic Screening Resistance / Marker	Eukaryotic Screening Resistance / Marker	Order
A01	Conventional Gene Synthesis Vector	MCS	Amp	N/A	Inquiry
A02	Conventional Gene Synthesis Vector	MCS	Kan	N/A	Inquiry
A03	Conventional Gene Synthesis + Prokaryotic-Induced Expression Vector	pTet:MCS	Amp	N/A	Inquiry
A04	Conventional Gene Synthesis + Prokaryotic-Induced Expression Vector	pLac:MCS	Amp	N/A	Inquiry
A05	Conventional Gene Synthesis Vector	MCS	CmR	N/A	Inquiry
A06	Conventional Gene Synthesis + Prokaryotic-Induced Expression Vector	pLac:MCS	Amp	N/A	Inquiry
A07	Conventional Gene Synthesis + Prokaryotic-Induced Expression + dsRNA IVT Vector	pT7:MCS:pS6	Amp	N/A	Inquiry
A08	Conventional Gene Synthesis + Prokaryotic-Induced Expression Vector	pLac:MCS	Amp	N/A	Inquiry
A09	Conventional Gene Synthesis + Prokaryotic-Induced Expression Vector	pLac:MCS	Kan	N/A	Inquiry
A10	Complex Gene Synthesis Vector	pLac:MCS	Amp	N/A	Inquiry
A11	Complex Gene Synthesis Vector	pLac:MCS	Kan	N/A	Inquiry

Expression Vectors

• Conventional Gene Expression VectorsView More

Vector Number	Species	Functional Description	Name	Prokaryotic Screening Resistance / Marker	Eukaryotic Screening Resistance / Marker	Order
Bm01	Mammal	The CMV promoter was initiated and the target gene was fused to the C-terminus of EGFP. It can be instantaneously transformed and stably transformed. Non-lentivirus packaging vector. The target cells were screened by green fluorescence and Neo.	pCMV:EGFP-MCS	Kan	Neo/EGFP	Inquiry
Bm02		The CMV promoter was initiated and the target gene was fused to the N-terminus of EGFP. It can be instantaneously transformed and stably transformed. Non-lentivirus packaging vector. The target cells were screened by green fluorescence and Neo.	pCMV:MCS-EGFP	Kan	Neo/EGFP	Inquiry
Bm03		CMV initiates the expression of the target gene, which is located at the N-terminus of EYFP. It can be transiently expressed or stably expressed. Non-lentiviral packaging vector, expressed only in eukaryotic cells. Cells were screened by Neo and EYFP.	pCMV:MCS-EYFP	Kan	Neo/EYFP	Inquiry
Bm04		CMV initiates the expression of the target gene, which is located at the N-terminus of ECFP. It can be transiently expressed or stably expressed, non-lentiviral packaging vector, expressed only in eukaryotic cells. Cells were screened by Neo and ECFP.	pCMV:MCS-ECFP	Kan	Neo/ECFP	Inquiry
Bm05		The CMV promoter was initiated and the target gene was fused to the N-terminus of EGFP. It can be instantaneously transformed and stably transformed. Non-lentivirus packaging vector, target cells were screened by green fluorescence and Neo.	pCMV:MCS-EGFP	Kan	Neo/EGFP	Inquiry
Bm06		The CMV promoter was initiated and the target gene was located at the N-terminus of EGFP. It can be instantaneously transformed or stably transformed. The non-lentiviral packaging vector can be expressed in both prokaryotic cells and eukaryotic cells. The target cells were screened by Kan / Neo.	pCMV-pT7:MCS-EGFP	Amp	Neo	Inquiry
Bm07		CMV initiates the expression of the target gene, which is located at the C-terminus of mCherry. It can be transiently expressed or stably expressed. Non-lentivirus packaging vector, expressed only in eukaryotic cells. Cells were screened by Neo and mCherry.	pCMV:mCherry-MCS	Kan	Neo/mCherry	Inquiry
Bm08		The CMV promoter was initiated, and the target gene was fused to the N-terminus of EGFP through IRES. It can be instantaneously transformed and stably transformed. Non-lentivirus packaging vector, target cells were screened by green fluorescence and Neo.	pCMV:MCS/IRES/EGFP	Kan	Neo/EGFP	Inquiry
Bm09		The CMV promoter was initiated, and the target gene was fused to the N-terminus of ZsGreen1 through IRES. It can be instantaneously transformed and stably transformed. Non-lentivirus packaging vector, target cells were screened by green fluorescence and Neo.	pCMV:MCS/IRES/ZsGreen1	Kan	Neo/ZsGreen1	Inquiry
Bm10		CMV initiates target gene expression. The target gene is fused to the N-terminus of DsRed by IRES. It can be transiently expressed and stably expressed. Non-lentivirus packaging vector, screening cells by Neo.	pCMV:MCS/IRES/DsRed	Kan	Neo/DsRed	Inquiry
Bm11		CMV initiates expression, and the C-terminus and C-terminus of DsRed2 contain ER targeting sequences. Non-lentiviral packaging vectors can be used to label the endoplasmic reticulum of living cells. The target protein is located at the C-terminal of DsRed2.	pCMV:DsRed-MCS	Kan	Neo/DsRed2	Inquiry
Bm12		There are two EF1a / CMV promoters that can initiate the expression of two target genes, respectively. It can be transiently expressed or stably expressed. Non-lentiviral packaging vector, containing Puro and DHFR screening marker genes, can be screened with MTX and Puro at the same time.	pCMV/EF1a:MCS-pCMV/EF1a:MCS	Kan	Puro/DHFR	Inquiry
Bm13		The target gene and copGFP were expressed by CMV and EF1a promoter, respectively. It can be instantaneously transformed and stably transformed. Lentivirus packaging, through green fluorescence detection, screening of target cells.	pCMV:MCS-pEF1:copGFP	Amp	copGFP	Inquiry
Bm14		CMV promoter initiates target gene expression. It can be instantaneously transformed and stably transformed. Lentivirus packaging can be performed. The target cells were screened by Puro resistance.	pCMV:MCS-pEF1:Puro	Amp	Puro	Inquiry
Bm15		The transcription of the target gene and the resistance gene Puro was initiated by the EF1a promoter. There is a T2A peptide between the target gene and the resistance gene, which can be self-cut at the translation level to ensure that the target gene and the resistance gene have the same translation level. The lentiviral packaging plasmid was pPACKH1. It can be transiently expressed or stably expressed. Lentiviral packaging vector, expressed only in eukaryotic cells. Cells were screened by Puro.	pEF1a:MCS/T2A/Puro	Amp	Puro	Inquiry
Bm16		EF1a initiates target gene expression. The copGFP / T2A / Puro expression was initiated by the CMV promoter. It can be transiently transformed and stably expressed. Lentivirus packaging vector, screening cells by copGFP and Puro.	pEF1a:MCS-pCMV:copGFP-T2A-Puro	Amp	Puro/copGFP	Inquiry
Bm17		It is initiated by the CMV promoter. The target gene was fused to the N-terminus of Hygro by IRES. It can be instantaneously transformed and stably transformed. Lentiviral packaging vector, target cells were screened by Hygro.	pCMV:MCS/IRES/Hygro	Amp	Hygro	Inquiry
Bm18		CMV initiates the expression of the target gene, which is located at the C-terminus of mCherry. It can be transiently expressed or stably expressed. Lentiviral packaging vector, expressed only in eukaryotic cells. Cells were screened by Puro and mCherry.	pCMV:mCherry-MCS	Amp	Puro/mCherry	Inquiry
Bm19		CMV initiates the expression of the target gene, which is fused to the N-terminus of AcGFP1 through IRES. It can be transiently expressed or stably expressed. Lentivirus packaging vector, screening cells by AcGFP1 and Puro.	pCMV:MCS/IRES/AcGFP1	Amp	Puro/AcGFP1	Inquiry
Bm20		CMV initiates target gene expression. It can be instantaneously transformed or stably transformed. Lentiviral packaging vector, the target cells were screened by Puro.	pCMV:MCS	Amp	Puro	Inquiry
Bm21		Tetracycline promoter (TRE3GS) regulates target gene expression (integrating regulation and response functions). It can be transiently expressed or stably expressed. Lentiviral packaging vector, expressed only in eukaryotic cells. Cells were screened by Puro.	pTRE3Gs:MCS	Amp	Puro	Inquiry
Bm22		The expression of target gene and resistance gene Puro was initiated by CMV promoter. There is an IRES sequence between the target gene sequence and the resistance gene, which can completely separate the two protein sequences, but the expression ability of the latter is lower than that of the former. It can be transiently expressed or stably expressed. Lentiviral packaging vector, expressed only in eukaryotic cells. Cells were screened by Puro.	pCMV:MCS/IRES/Puro	Amp	Puro	Inquiry
Bm23		The target gene expression was initiated by the EF1a promoter, and the C-terminus of the target gene was fused with GFP. Lentivirus packaging can be performed.	pEF1a:MCS/EGFP	Amp	GFP	Inquiry
Bm24		Two CMV promoters were used to initiate the simultaneous expression of the target gene and GFP. Low copy expression vector can be used for adenovirus packaging.	pCMV:MCS-pCMV:GFP	Kan	EGFP	Inquiry
Bp01	Plant	Two 35S promoters were used to initiate the expression of target gene and GUS gene, respectively. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:MCS-p35S:GUS	Kan	Hygro	Inquiry
Bp02		The 35S promoter initiates the expression of the target gene. The C-terminal of the target gene was fused with EGFP protein. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:MCS/EGFP	Kan	Hygro/EGFP	Inquiry
Bp03		The UBi promoter initiates target gene expression. The 35S promoter initiates EGFP expression. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	pUbi:MCS-p35S:EGFP	Kan	EGFP	Inquiry
Bp04		The 35S promoter initiates the expression of mCherry fluorescence located in the Golgi apparatus. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:mCherry/Golgi	Kan	Hygro/mCherry	Inquiry
Bp05		The 35S promoter initiates ER / CFP gene expression. CFP fluorescence was localized in the endoplasmic reticulum. It can be transiently expressed or stably expressed in plant cells by Agrobacterium transfection.	p35S:ER/CFP	Kan	Hygro/CFP	Inquiry
Bp06		The 35S promoter initiates NES / mCherry gene expression. mCherry is located in the cytoplasm. It can be transiently expressed or stably expressed in plant cells by Agrobacterium transfection.	p35S:NES/mCherry	Kan	Hygro/mCherry	Inquiry
Bp07		35S initiates target gene expression. The N-terminus of the target gene contains a mitochondrial guidance signal, and the C-terminus is fused with mCherry. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:Mito/MCS/mCherry-p35S:Hygro	Kan	Hygro/mCherry	Inquiry
Bp08		35S initiates the expression of CFP in the nucleus. The N-terminal of CFP contains NLS signal. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:NLS/CFP	Kan	Neo+/CFP	Inquiry
Bp09		The 35S promoter initiates the expression of the target gene. The N-terminal of the target gene was fused with EGFP protein. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:EGFP/MCS-p35S:Neo	Kan	Neo+	Inquiry
Bp10		The 35S promoter initiates the GFP signal to localize on the cell membrane. It can be transiently transformed or transfected into plant cells by Agrobacterium for stable expression.	p35S:EGFP/PM-signal	Kan	Neo+/EGFP	Inquiry
Bp11		The 35S promoter initiates the expression of the target gene. The C-terminus of the target gene was fused with YFP. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:MCS/YFP	Kan	Neo+/YFP	Inquiry
Bp12		The 35S promoter initiates the expression of the target gene. The C-terminus of the target gene was fused with mCherry. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p35S:MCS/mCherry	Kan	Neo+/mCherry	Inquiry
Bp13		The 35S promoter initiates the expression of the target gene. The C-terminus of the target gene was fused with CFP. It can be transiently expressed, and can also be transfected into plant cells by Agrobacterium for stable expression.	p36S:MCS/CFP	Kan	Neo+/CFP	Inquiry
Bl01	Lactobacillus / Lactococcus lactis	The p32 promoter initiates target gene expression, constitutive expression, and low-copy vector.	p32:MCS	Ery+/Chloramphenicol	NA	Inquiry
Bl02		The PnisA promoter initiates target gene expression. The expression host was NZ9000 Lactococcus lactis. Medium copy expression vector, the vector must use MC1601 competent state in amplification and propagation.	pnis:MCS	Chl+	NA	Inquiry
Bl03		The p59 promoter initiates the expression of the target gene. It has a secretory signal peptide and nucA, which is conducive to the anchoring of the target protein on the cell surface after secretion, and belongs to the secretory expression vector.	p59:PSusp/nucA-MCS	Amp+	Ery+	Inquiry
Bi01	Insect	Polyhedrin promoter initiates target gene expression. The N-terminus of the target gene is connected with the GUS gene.	pPH:GUS-MCS	Amp+	GUS	Inquiry
Bi02	Insect	Polyhedrin promoter initiates target gene expression. The N-terminus of the target gene contains a His tag and a TEV site, and the N-terminus is fused with GFP protein.	pPH:6*His-TEV site-MCS/EGFP	Amp+	EGFP/GmR	Inquiry
Bsa01	Saccharomyces Cerevisiae	The GAL1 promoter induced by galactose initiates the expression of the target gene. The C-terminal of the target gene was fused with GFP protein.	pGAL1:MCS/EGFP	Amp+	URA3	Inquiry
Bst01	staphylococcus aureus	The Rpsl promoter initiates mCherry expression.	pRpsl:RBS/mCherry	Amp+/Chl+/mCherry	NA	Inquiry

• Recombinant Protein Expression VectorsView More

Vector Number	Species	Functional Description	Name	Prokaryotic Screening Resistance / Marker	Eukaryotic Screening Resistance / Marker	Order
Cm01	Mammal	The CMV promoter initiates the expression of the target gene in mammalian cells. There is a T7 promoter sequence at the front end of the target sequence. Non-viral vectors can also be used as in vitro transcription vectors.	pCMV-pT7:MCS	Amp	Hygro	Inquiry
Cm02		The CMV promoter initiates the expression of the target gene in mammalian cells. There is a T7 promoter sequence at the front end of the target sequence. Non-viral vectors can also be used as in vitro transcription vectors.	pCMV-pT7:MCS	Amp	NeoR/KanR	Inquiry
Cm03		The CMV promoter initiates the expression of the target gene in mammalian cells. There is a T7 promoter sequence at the front end of the target sequence. Non-viral vectors can also be used as in vitro transcription vectors.	pCMV-pT7:MCS	Amp	NeoR/KanR	Inquiry
Cm04		The CMV promoter initiates the expression of the target gene in mammalian cells. The target sequence has a T7 promoter sequence at the front end, and the C-terminal of the target protein is fused with Myc and 6 * His tags. Non-viral vector.	pCMV-pT7:MCS/Myc/6×His	Amp	NeoR/KanR	Inquiry
Cm05		The CMV promoter initiates the expression of the target gene in mammalian cells. The C-terminal of the target gene is connected with WPRE, and the C-terminal region of WPRE contains a Factor Xa site. Non-viral vector.	pCMV:MCS-WPRE(Factor Xa site)	Amp	NeoR/KanR	Inquiry
Cm06		The CMV promoter initiates the expression of the target gene in mammalian cells, and the C-terminal of the target gene is connected with WPRE. The target sequence can be connected to the carrier by Topo connection method.	pCMV:Topo site-WPRE	Amp	Neo	Inquiry
Cm07		CMV-IE initiates target gene expression. Mammalian high-efficiency expression vector, no eukaryotic screening resistance, no fluorescent gene. Transient expression vector and non-viral vector.	pCMV-IE:MCS	Amp	N/A	Inquiry
Cm08		The CMV promoter initiates the expression of the target gene in mammalian cells. There is a T7 promoter sequence at the front end of the target sequence. Non-viral vectors can also be used as in vitro transcription vectors.	pCMV-pT7:MCS	Amp	Hygro	Inquiry
Cm09		The CMV-IE promoter initiates the expression of the target gene, which is regulated by tetracycline. Non-viral vector.	pCMV-IE:MCS/Tet-On 3G	Amp/Kan	NeoR/KanR	Inquiry
Cm10		The CMV promoter initiates the expression of the target gene in mammalian cells. No eukaryotic screening resistance, no fluorescent tags. Transient expression vector, containing NotI restriction sites. Through this site, the expression cassette can be cut off and subcloned into the ITR-containing vector.	pCMV:MCS	Amp	N/A	Inquiry
Cm11		The CMV promoter initiates the expression of the target gene in mammalian cells. The target sequence has a T7 promoter sequence at the front end, and the C-terminal of the target gene is fused with Myc and 6 * His tags. Non-viral vectors can also be used as in vitro transcription vectors.	pCMV-pT7:MCS/Myc/6×His	Amp/BSD	BSD	Inquiry
Cm12		The CMV promoter initiates the expression of the target gene in mammalian cells. In vitro transcription vector, the sense strand RNA or antisense strand RNA of the target gene was obtained by in vitro transcription under the action of T7 polymerase or SP6 polymerase. Non-viral vector.	pCMV-pT7:MCS-pSP6	Amp	NeoR/G418	Inquiry
Cm13		The CMV promoter initiates the expression of the target gene in mammalian cells. There is a T7 promoter sequence at the front end of the target sequence. The C-terminus of the target gene was fused with Myc and Flag tags. It can also be used as an in vitro transcription vector.	pCMV-pT7:MCS/Myc/Flag	Kan	NeoR/G418	Inquiry
Cm14		The simultaneous expression of two target genes was initiated by two CMV promoters, respectively. Transient expression vector.	pCMV1:MCS1-pCMV2:MCS2	Amp	N/A	Inquiry
Cm15		Cell surface display carrier. CMV initiates target protein expression. The N-terminus of the target protein contains IgK leader sequence to guide extracellular secretion, and the C-terminus has a membrane localization signal PDGFP, which is located on the cell membrane.	pCMV:IgK leader/MCS/PDGFR	Amp	NeoR	Inquiry
Ce01	E.coli	T7 promoter initiates target gene expression. The T7 tag was fused at the N-terminus of the target gene. Transient expression and constitutive expression.	pT7:T7 tag-MCS	Kan	N/A	Inquiry
Ce02		T7 promoter initiates target gene expression. The T7 tag was fused at the N-terminus of the target gene. 6 * His fused to the C-terminus of the target gene. Transient expression and constitutive expression.	pT7:T7 tag/MCS/6*His	Amp	N/A	Inquiry
Ce03		T7 promoter initiates target gene expression. The target gene contains a pelB signal peptide at the N-terminus and a 6 * His at the C-terminus. The target protein is located in periplasm.	pT7:pelB-MCS/6*His	Amp	N/A	Inquiry
Ce04		T7 promoter initiates target gene expression. There is a T7 tag at the N-terminus of the target gene.	pT7:T7 tag/MCS	Amp	N/A	Inquiry
Ce05		T7 promoter initiates target gene expression. The N-terminus of the target gene contains a T7 tag.	pT7:T7 tag/MCS	Amp	N/A	Inquiry
Ce06		T7 promoter initiates target gene expression. The N-terminal of the target gene contains 6 * His tag, T7 tag, Xpress antigen recognition site and EK site in turn.	pT7:6*His/T7 tag/Xpress Epitope/EK/MCS	Amp	N/A	Inquiry
Ce07		Two T7lac promoters were induced by IPTG to initiate the simultaneous expression of the two target genes. One of the target genes was fused with the 8 * His tag at the N-terminus, and the other target gene was fused with the S-Tag tag at the C-terminus. Two target gene co-expression vectors, transient expression and non-viral vectors.	pT7lac:8*His/MCS1-pT7lac:MCS2/S-Tag; 含有placI:lacI	CmR	N/A	Inquiry
Ce08		In the cold environment, IPTG was applied to induce the expression of the target gene. The N-terminus of the target gene was fused with a 6 × His tag. Transient expression, non-viral vector.	pcspAlac:6×His/MCS	Amp	N/A	Inquiry
Ce09		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene has a 6 * His Tag, and there is a Thrombin cleavage site between the 6 * His tag and the target gene. High expression vector, transient expression and constitutive expression.	pT7lac:6*His-a thrombin site-MCS	Amp	N/A	Inquiry
Ce10		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal of the target gene has a 10 * His Tag, and there is an enterokinase cleavage site between the 10 * His tag and the target gene. High expression vector, transient expression and constitutive expression.	pT7lac:10*His-a enterokinase site-MCS	Amp	N/A	Inquiry
Ce11		IPTG was applied to induce T7 promoter to initiate target gene expression. The target gene contains a T7 tag at the N-terminus and a 6 * His tag at the C-terminus.	pT7lac:T7 tag/MCS/6*His	Amp	N/A	Inquiry
Ce12		IPTG was applied to induce T7 promoter to initiate target gene expression. The target gene contains a T7 tag at the N-terminus and a 6 * His tag at the C-terminus.	pT7lac:T7 tag/MCS/6*His	Amp	N/A	Inquiry
Ce13		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene contains a pelB signal peptide, which makes the target protein localized to the periplasm. The C-terminal of the target protein contains a 6 * His tag.	pT7lac:pelB/MCS/6*His	Amp	N/A	Inquiry
Ce14		IPTG was applied to induce T7 promoter to initiate target gene expression. The target gene contains a T7 tag at the N-terminus and a 6 * His tag at the C-terminus.	pT7lac:T7 tag/MCS/6*His	Kan	N/A	Inquiry
Ce15		T7 promoter initiates target gene expression. The target gene contains a pelB signal peptide at the N-terminus and a 6 * His at the C-terminus. The target protein is located in periplasm.	pT7lac:pelB/MCS/6*His	Kan	N/A	Inquiry
Ce16		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal of the target gene contains 6 * His, T7 tag, and the C-terminal contains 6 * His tag. There is a thrombin cleavage site between the N-terminal 6 * His and the T7 tag.	pT7lac:6His/a thrombin site/T7 tag/MCS/6His	Kan	N/A	Inquiry
Ce17		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal of the target gene contains 6 * His, T7 tag, and the C-terminal contains 6 * His tag. There is a thrombin cleavage site between the N-terminal 6 * His and the T7 tag.	pT7lac:6His/a thrombin site/T7 tag/MCS/6His	Kan	N/A	Inquiry
Ce18		IPTG was applied to induce T7 promoter to initiate target gene expression. The target gene contains an S tag at the N-terminus and a 6 * His tag at the C-terminus. There is a thrombin cleavage site between the S tag and the target gene.	T7lac:S Tag/a thrombin site/MCS/6*His	Kan	N/A	Inquiry
Ce19		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal of the target gene contains a 6 * His tag, the S-tag, and the C-terminal contains a 6 * His tag. There is a thrombin site between 6 * His and S-tag. There is an enterokinase cleavage site between the S-tag and the target gene.	pT7lac:6His/a thrombin site/S tag/enterokinase site/MCS/6His	Kan	N/A	Inquiry
Ce20		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal of the target gene contains a 6 * His tag, the S-tag, and the C-terminal contains a 6 * His tag. There is a thrombin site between 6 * His and S-tag. There is an enterokinase cleavage site between the S-tag and the target gene.	pT7lac:6His/a thrombin site/S tag/enterokinase site/MCS/6His	Kan	N/A	Inquiry
Ce21		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene contains TrxA ( thioredoxin A ) to promote soluble protein expression, 6 * His tag and S-tag. The C-terminus contains a 6 * His tag. There is a thrombin site between the N-terminal 6 * His tag and the S tag. There is an enterokinase site between the S-tag and the target gene.	pT7lac:TrxA-6His/a thrombin site/S-Tag/enterokinase site/MCS/6His	Amp	N/A	Inquiry
Ce22		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene contains DsbC ( disulfide isomerase ) to promote soluble protein expression, 6 * His tag and S-tag. The C-terminus contains an 8 * His tag. There is a thrombin site between the N-terminal 6 * His tag and the S tag. There is an enterokinase site between the S-tag and the target gene.	pT7lac:DsbC/6His/a thrombin site/S-Tag/enterokinase site/MCS/8His	Kan	N/A	Inquiry
Ce23		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene contains GST tag, 6 * His and S-Tag. The C-terminus contains an 8 * His tag. There is a thrombin site between the N-terminal 6 * His and S-Tag. There is an enterokinase site between the S-tag and the target gene.	pT7lac:GST/6His/a thrombin site/S-Tag/enterokinase site/MCS/8His	Kan	N/A	Inquiry
Ce24		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene contains a 6 * His tag and the C-terminus contains an S-tag tag. There is an enterokinase site between the target gene and 6 * His.	pT7lac:6*His/enterokinase site/MCS/S-Tag	Amp	N/A	Inquiry
Ce25		IPTG was applied to induce T7 promoter to initiate target gene expression. The C-terminus of the target gene contains a 6 * His tag.	pT7lac:MCS/6*His	Amp	N/A	Inquiry
Ce26		IPTG was applied to induce the simultaneous expression of two target genes by two T7 promoters. The N-terminal of one target gene contains a 6 * His tag, and the C-terminal of the other target gene contains a S Tag tag.	pT7lac:6*His/MCS-pT7lac:MCS/S-Tag	Amp	N/A	Inquiry
Ce27		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal and C-terminal of the target gene have a 6 * His tag, respectively.	pT7lac:6His/MCS/6His	Kan	N/A	Inquiry
Ce28		IPTG was applied to induce T7 promoter to initiate target gene expression. The C-terminus of the target gene was fused with Mxe intein and CBD. The fusion protein could bind to chitin (CBD) magnetic beads. Thiol-induced Mxe intein cleavage activity releases the target protein.	pT7lac:MCS/Mxe intein/CBD	Amp	N/A	Inquiry
Ce29		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminal of the target gene contains 6 * His tag, 6 * His tag and S-Tag tag in turn. There is a NusA between the two 6 * His tags to help the target protein soluble. There is a thrombin cleavage site and an enterokinase site between S-Tag and the target gene. The C-terminus of the target gene contains a HSV tag and a 6 * His tag.	pT7lac:6His/NusA/6His/S-Tag/a thrombin site/enterokinase site/MCS/HSV tag/6*His	Amp	N/A	Inquiry
Ce30		IPTG was applied to induce T7 promoter to initiate target gene expression. The N-terminus of the target gene contains a 6 * His tag, a thrombin site, and a SUMO tag. SUMO tag can promote the solubility of the target protein. As a chaperone protein, it can promote the correct folding of protein and enhance the tolerance of target protein to heat and protease. It can also shield the toxicity of some toxic proteins to host bacteria. The C-terminus of the target protein contains a 6 * His tag.	pT7lac:6His/thrombin site/SUMO/MCS/6His	Kan	N/A	Inquiry
Ce31		IPTG was applied to induce T5 promoter to initiate target gene expression. The C-terminus of the target gene contains a 6 * His tag.	pT5lac:MCS/6*His	Amp	N/A	Inquiry
Ce32		IPTG was applied to induce T5 promoter to initiate target gene expression. The N-terminus of the target gene contains a 6 * His tag. Low copy vector.	pT5lac:6*His/MCS	Amp	N/A	Inquiry
Ce33		IPTG was applied to induce the tac promoter to initiate the target gene expression. Low expression can reduce the probability of forming inclusion bodies, low copy vector.	ptac:MCS	Amp	N/A	Inquiry
Ce34		IPTG was applied to induce the tac promoter to initiate the target gene expression. The N-terminus of the target gene contains MBP to localize the protein in the periplasm. There is a Factor Xa site between the target gene and MBP.	ptac:MBP/Factor Xa site/MCS	Amp	N/A	Inquiry
Ce35		IPTG was applied to induce the tac promoter to initiate the target gene expression. The N-terminus of the target gene contains MBP to localize the protein in the periplasm. There is a Factor Xa site between the target gene and MBP.	ptac:MBP/Factor Xa site/MCS	Amp	N/A	Inquiry
Ce36		IPTG was applied to induce the CSPA promoter to initiate the target gene expression under cold environment treatment. The N-terminus of the target gene contains a TEE tag.	pCSPAlac:TEE/MCS	Amp	N/A	Inquiry
Ce37		Application of arabinose induced araBAD promoter to initiate target gene expression. The N-terminus of the target gene contains a 6 * His tag. In glucose-free medium, arabinose positively regulates the expression of target genes. The soluble expression of the target protein was optimized by adjusting the concentration level of arabinose.	pBAD:MCS/Myc/6*His	Amp	N/A	Inquiry
Ce38		Lac initiates the expression of Trc promoter. The N-terminus of the target protein contains 6 His purification tags for protein purification. There is a rTEV protease recognition site between the His tag and the target protein, which can be digested by rTEV protease to remove the fused His tag.	pLacTrc:6*His-rTEV protease cleavage site-MCS	Amp	N/A	Inquiry
Cpy01	Yeast	Pichia pastoris protein expression vector and integrated vector. GAP promoter initiates target gene expression. The N-terminus of the target gene contains an α-factor secretion signal peptide to secrete the target protein. The C-terminus of the target gene contains a Myc tag and a 6 * His tag.	pGAP:α factor/MCS/Myc/6*His	Zeo	Zeo	Inquiry
Cpy02		Pichia pastoris expression vector. The AOX1 promoter initiates target gene expression. The N-terminus of the target gene contains an α-factor secretion signal peptide to secrete the target protein.	pAOX1:α factor/MCS	Amp	Kan/HIS4	Inquiry
Cpy03		Pichia pastoris expression vector. The AOX1 promoter initiates target gene expression. The N-terminus of the target gene contains an α-factor secretion signal peptide to secrete the target protein. The C-terminus of the target gene contains a Myc tag and a 6 * His tag.	pAOX1:α factor/MCS/Myc/6*His	Zeo	Zeo	Inquiry
Csa01		Saccharomyces cerevisiae expression vector. Galactose induced the GAL1 promoter to initiate the expression of the target gene at a high level, and glucose inhibited the expression.	pGAL1-pT7:MCS	Amp	URA3	Inquiry
Csa02		Saccharomyces cerevisiae surface display vector. GAL1 initiates the expression of AGA2 expression cassette. The target protein is inserted into the AGA2 expression box and needs to be expressed in Saccharomyces cerevisiae containing Aga1 to achieve surface display.	pGAL1-pT7:AGA2/GS linker Xpress/MCS/V5 epitope 6*His	Amp	TRP1	Inquiry
Ci01	Insect	Baculovirus expression system vector. There are two promoters of P10 and Polyhedrin on the vector, which respectively initiate the expression of the target gene and realize the simultaneous expression of the two genes on a single vector.	pP10:MCS-pPH:MCS	Amp	Gent	Inquiry
Ci02		Polyhedrin promoter initiates target gene expression. The N-terminus of the target gene contains a 6 * His tag. There is a TEV cleavage recognition site between the target gene and the 6 * His tag.	pPH:6*His/TEV/MCS	Amp	Gent	Inquiry
Ci03		Polyhedrin promoter initiates target gene expression. The N-terminus of the target gene contains a 6 * His tag. There is a TEV cleavage recognition site between the target gene and the 6 * His tag.	pPH:6*His/TEV/MCS	Amp	Gent	Inquiry
Ci04		Polyhedrin promoter initiates target gene expression. The N-terminus of the target gene contains a 6 * His tag. There is a TEV cleavage recognition site between the target gene and the 6 * His tag. The C-terminus of the target gene contains a Flag tag.	pPH:6*His/TEV/MCS/Flag	Amp	Gent	Inquiry
Ci05		Polyhedrin promoter initiates target gene expression. No fusion protein tag. The target sequence needs to contain the start codon and the stop codon. Insect expression vector and baculovirus expression vector.	pPH:MCS	Amp	Gent	Inquiry
Cb01	bacillus subtilis	Grac induced by IPTG initiates target gene expression. Highly efficient expression of recombinant foreign protein in Bacillus subtilis.	pGracLac:MCS	Amp/Chloramphenicol	N/A	Inquiry
Cb02	bacillus subtilis	Grac induced by IPTG initiates the expression of the target gene and can secrete and express the recombinant protein at a high level. The pGrac sequence contains the SD sequence and the lacO operator sequence.	pGracLac:SamyQ/MCS	Amp/Chloramphenicol	N/A	Inquiry
Csal01	salmonella	GFP was induced and mCherry was constitutively expressed.	pBAD:GFP-prpsM:mCherry	Amp/mCherry/GFP	N/A	Inquiry

Expression Regulatory Vectors

• Activating & Inhibiting Expression Vectors View More

Vector Number	Species	Functional Description	Name	Prokaryotic Screening Resistance / Marker	Eukaryotic Screening Resistance / Marker	Order
GAm01	Mammal	The promoter EF-1α initiates dCas9-VP64-2A-Blast expression. Lentivirus packaging and Blast screening resistance can be performed. SAM activation system, three-vector system (vector 1).	pEF-1α:dCas9/VP64/Blast	Amp	Blast	Inquiry
GAm02		The promoter EF-1α initiates the expression of dCas9-VP64 / EGFP. Lentivirus packaging and EGFP fluorescence screening can be performed. SAM activation system, three-vector system (vector 1).	pEF-1α:dCas9/VP64/EGFP	Amp	EGFP	Inquiry
GAm03		The promoter EF-1α initiates the expression of the activation element MS2-P65-HSF1, which can be used for lentivirus packaging and Hygro screening resistance. SAM activation system, three-vector system (vector 2).	pEF-1α:MS2-P65-HSF1	Amp	Hygro	Inquiry
GAm04		The promoter U6 initiates the expression of sgRNA and regulatory element MS2 stem loop. Lentivirus packaging and TagBFP fluorescence screening can be performed. SAM activation system, three-vector system (vector 3).	pU6:sgRNA-MS2 stem loop	Amp	Puro/TagBFP	Inquiry
GAm05		Promoter U6 initiates sgRNA / MS2 stem loop expression. The promoter EF-1α initiates dCas9 / VP64 expression. Puro screening resistance. SAM dual-vector activation system (vector 1). Lentivirus packaging can be performed.	pU6:sgRNA/MS2 stem loop-pEF-1α:dCas9-VP64	Amp	Puro	Inquiry
GAm06		The promoter EF-1α initiates the expression of the activation element MS2-P65-HSF1. Lentivirus packaging can be performed. Neo / G418 screening resistance. SAM activation system, double vector system (vector 2).	pEF-1α:MS2-P65-HSF1	Amp	Neo/G418	Inquiry
GAm07		All-in-one CRISPRa vector (single plasmid system). Lentivirus packaging can be performed. SAM activation system, single vector system, screened by Blast.	pU6:sgRNA(MS2)-pEF-1α:dCas9/VP64-p65-HSF1/Blast	Amp/BleoR	Blast	Inquiry
GAm08		The promoter EF-1α initiates dCas9-VPR / EGFP expression. Lentivirus packaging and EGFP fluorescence screening tags can be performed. VPR dual-vector activation system (vector 1). A complete VPR activation system is formed with a gRNA vector.	pEF-1a:dCas9-VPR/EGFP	Amp	EGFP	Inquiry
GAm09		The promoter EF-1a initiates dCas12a-VPR / Puro expression. Lentivirus packaging and Puro screening tags can be performed. VPR dual-vector activation system (vector 1). A complete VPR activation system is formed with a gRNA vector.	pEF-1a:dCas12a-VPR/Puro	Amp	Puro	Inquiry
GAm10		The promoter EF-1α initiates the expression of SaCas9-VPR, contains gRNAscaffold, and can insert sgRNA promoter in the MCS region. Lentivirus packaging and Puro screening can be performed. VPR single vector activation system.	MCS:sgRNA-pEF-1α:SaCas9-VPR	Amp/BleoR	Puro	Inquiry
GIm01	Mammal	RNAi regulation efficiency detection vector. The T7 promoter initiates the expression of the target gene, and the N-terminal of the target gene contains hRluc protein. The target gene was cloned to the multiple cloning site downstream of the renilla luciferase translation termination codon. RNAi of the target gene, initiated by synthetic siRNA or in vivo expressed shRNA, leads to cleavage and subsequent degradation of the fused mRNA. Detecting the decrease of renilla luciferase activity is a simple method to monitor the effect of RNAi.	pT7:hRluc/MCS-pHS-TK:hluc+	Amp	hRluc/hluc+	Inquiry
GIm02		N/A	N/A	N/A	N/A	Inquiry
GIm03		CRISPR inhibition vector. All-in-one vector. The UbC promoter initiates dCas9 and the inhibitory element KRAB expression, and the U6 promoter initiates sgRNA expression. Lentivirus packaging can be performed.	pUbC:dCas9/KRAB-pU6:sgRNA	Amp	Puro	Inquiry
GIm04		CRISPR sgRNA vector, which is suitable for CRISPR inhibition or activation of dual vector system, can be used for lentivirus packaging. The vector does not contain Cas9 protein, and needs to complete the activation or inhibition function together with the vector containing Cas9 and activation or inhibition elements.	pmU6:sgRNA-pEF1a:Puro/TagBFP	Amp	Puro/BFP	Inquiry
GIm05		The CRISPR double vector inhibition system, dCas9-KRAB vector, no sgRNA, and sgRNA vector constitute the inhibition system. Lentivirus packaging can be performed.	pSFFV:dCas9-TagBFP-KRAB	Amp	TagBFP	Inquiry
GIm06		CRISPR dual vector inhibition system, KRAB-dCas9 vector, no sgRNA, and sgRNA vector form an inhibition system. Lentivirus packaging can be performed.	pSFFV:KRAB-dCas9/mCherry	Amp	mCherry	Inquiry
GIm07		RNAi expression vector, siRNA expression vector, transient expression vector. H1 promoter initiates the expression of target siRNA.	pH1:MCS	Amp	N/A	Inquiry
GIm08		RNAi expression vector, siRNA expression vector. H1 promoter initiates the expression of target siRNA.	pH1:MCS	Amp	Hygro	Inquiry
GIm09		RNAi expression vector, siRNA expression vector. CMV promoter initiates the expression of target siRNA.	pCMV:MCS	Amp	Neo	Inquiry
GIm10		RNAi vector, siRNA expression vector, low-copy vector. Lentivirus packaging can be performed.	pU6:MCS	Amp	Puro	Inquiry
GIm11		RNAi vector, tetracycline-induced shRNA expression vector.	pTightU6:MCS	Amp	Neo	Inquiry
GIm12		RNAi vector, transient expression vector. H1 promoter initiates RNA expression.	pH1:MCS-pPGK:EGFP/Neo	Amp	Neo/EGFP	Inquiry
GIm13		RNAi vector, shRNA expression vector. Lentivirus packaging can be performed. H1 promoter initiates the expression of target shRNA.	pH1:MCS-pEF1a:EGFP	Amp	EGFP	Inquiry
GIm14		RNAi vector, shRNA expression vector. Lentivirus packaging can be performed. U6 promoter initiates target gene expression. The target sequence expression can be achieved by replacing the stuffer region in the vector with the target sequence.	pU6:Stuffer-phPGK:Puro	Amp	Puro	Inquiry
GIm15		RNAi vector, shRNA expression vector. Lentivirus packaging can be performed. U6 promoter initiates target gene expression. CMV promoter initiates EGFP expression. hPGK initiates Puro expression.	pU6:MCS-pCMV:EGFP-phPGK:Puro	Amp	Puro/EGFP	Inquiry
GIp01	Plant	RNAi vector. 35S initiates RNA expression. It can be transiently expressed or stably expressed.	p35S:MCS1-chsA intron-MCS2	Kan	Bar+	Inquiry
GIp02		RNAi vector, transient expression vector. 35S initiates RNA expression.	p35S:MCS1-PDK intron-MCS2	Amp	N/A	Inquiry
GIp03		RNAi vector, transient expression vector. 35S initiates RNA expression.	p35S:MCS1-PDK intron-MCS2	Kan	N/A	Inquiry
GIp04		RNAi vector. UBi-1 initiates RNA expression. It can be transiently expressed or stably expressed.	pUBi-1:MCS1-rice intron-MCS2	Kan	Hygro/GUS	Inquiry
GInem01	Nematodes	RNAi vector, transient expression vector. Two T7 promoters bidirectionally initiate RNA expression.	pT7:MCS1-MCS2:pT7	Amp	N/A	Inquiry
GIfu01	Fungi	RNAi vector. TrpC promoter initiates RNA expression. It can be transiently expressed or stably expressed.	pTrpC:MCS1-IT-MCS2	Amp	Hygro	Inquiry

In Vitro Transcription Vectors

• In Vitro Transcription VectorsView More

Vector Number	Species	Functional Description	Name	Prokaryotic Screening Resistance / Marker	Eukaryotic Screening Resistance / Marker	Order
H01	N/A	mRNA in vitro transcription vector. The vector contains a polyA sequence. The target sequence is added in front of the polyA sequence (such as the BbsI restriction site). The target sequence should contain T7 promoter, 5'UTR, and 3'UTR, while the BspQI restriction site should be avoided in the target sequence.	MCS:polyA	Kan+	N/A	Inquiry
H02	N/A	mRNA in vitro transcription vector. The vector contains a polyA sequence. The target sequence is added in front of the polyA sequence (such as the BbsI restriction site). The target sequence of the vector should contain T7 promoter, 5'UTR, and 3'UTR, while the MluI restriction site should be avoided in the target sequence.	MCS:polyA	Kan+	N/A	Inquiry
H03	Mammal	mRNA in vitro transcription vector and transient expression vector. It contains T7 promoter, 5'UTR, and 3'UTR sequences suitable for mammalian cells (human, mouse), and contains a polyA sequence. The target gene sequence is inserted at the EcoRI site, and the HA tag sequence is contained behind the EcoRI site, which can be used to label the target protein.	pCMV/pT7:5'UTR-EcoRI-HA-3’UTR-polyA	Kan+	N/A	Inquiry
H04	Mammal	mRNA in vitro transcription vector and transient expression vector. It contains T7 promoter, 5'UTR, and 3'UTR sequences suitable for mammalian cells (human, mouse), and contains a polyA sequence. The target gene sequence is inserted into the EcoRI site, which contains the HA tag sequence and the EGFP sequence after the EcoRI site, which can be used to mark the target protein.	pCMV/pT7:5'UTR-EcoRI-HA/EGFP-3’UTR-polyA	Kan+	N/A	Inquiry

Editing Vectors

• DNA Editing VectorsView More

Vector Number	Species	Functional Description	Name	Prokaryotic Screening Resistance / Marker	Eukaryotic Screening Resistance / Marker	Order
Em01	Mammal	All-in-one vector. The EF1α promoter initiates Cas9 expression, the U6 promoter initiates sgRNA expression, and is screened with Puro. Lentivirus packaging can be performed.	pU6:sgRNA-pEF1a:Cas9	Amp	Puro	Inquiry
Em02		All-in-one vector. The EF1α promoter initiates Cas9 expression, the U6 promoter initiates sgRNA expression, and GFP is used for screening. Lentivirus packaging can be performed.	pU6 :sgRNA-pEF1a:Cas9	Amp	EGFP	Inquiry
Em03		All-in-one vector. EF1αpromoter initiates Cas9 expression and U6 promoter initiates sgRNA expression, which can be screened by mCherry and Puro. Lentivirus packaging can be performed.	pU6:sgRNA-pEF1a:Cas9	Amp	Puro/mCherry	Inquiry
Em04		Cas9 vector. The EF1α promoter initiates Cas9 expression. Lentivirus packaging can be performed.	pEF1a:Cas9	Amp	Blast	Inquiry
Em05		Cas9 vector. Tetracycline induced Tight Tre promoter to initiate Cas9 expression. Blast can be used for screening. Lentivirus packaging can be performed.	pTight Tre:Cas9	Amp	Blast	Inquiry
Em06		sgRNA vector. U6 promoter initiates sgRNA expression. Puro can be used for screening. Lentivirus packaging can be performed.	pU6:sgRNA	Amp	Puro	Inquiry
Em07		sgRNA vector. U6 promoter initiates sgRNA expression. Puro and DsRed can be used for screening. Lentivirus packaging can be performed.	pU6:sgRNA	Amp	Puro/DsRed	Inquiry
Em08		sgRNA vector. U6 promoter initiates sgRNA expression. Puro and GFP can be used for screening. Lentivirus packaging can be performed.	pU6:sgRNA	Amp	Puro/EGFP	Inquiry
Em09		sgRNA vector, single cell sequencing vector. U6 promoter initiates sgRNA expression. Puro can be used for screening. Lentivirus packaging can be performed.	pU6:sgRNA	Amp	Puro	Inquiry
Em10		All-in-one vector. The CMV promoter initiates SaCas9 expression, and the U6 promoter initiates Sa-gRNA expression. No screening label. Adeno-associated virus packaging can be performed.	pCMV:SaCas9-pU6:Sa-gRNA	Amp	N/A	Inquiry
Em11		All-in-one vector. The CMV promoter initiates SaCas9 expression, and the U6 promoter initiates Sa-gRNA expression. You can use mCherry to filter. Adeno-associated virus packaging can be performed.	pCMV:SaCas9-pU6:Sa-gRNA	Amp	mCherry	Inquiry
Em12		Sa-sgRNA vector. U6 promoter initiates sa-gRNA expression, and CMV initiates EGFP expression. EGFP can be used for screening. AAV packaging can be carried out.	pU6:sa-gRNA-pCMV:EGFP	Amp	EGFP	Inquiry
Em13		Sp-sgRNA vector. U6 promoter initiates sp-gRNA expression, and hSyn initiates EGFP expression. EGFP can be used for screening. AAV packaging can be carried out.	pU6:sp-gRNA-phSyn:EGFP	N/A	N/A	Inquiry
Em14		All-in-one vector, double sgRNA vector. Two U6 promoters are used to initiate the simultaneous expression of two sgRNAs, and the Cbh promoter is used to initiate Cas9 expression, which is a non-viral vector.	pU6:sgRNA-pU6:sgRNA-pCbh:Cas9	Amp	N/A	Inquiry
Em15		Cas9 vector. The Cbh promoter initiates Cas9 expression. Puro can be used for screening, non-viral vector.	pCbh:Cas9	Amp	Puro	Inquiry
Em16		Cas9 vector. The Cbh promoter initiates Cas9 expression. GFP can be used for screening, non-viral vector.	pCbh:pCas9	Amp	GFP	Inquiry
Em17		sgRNA vector. U6 promoter initiates sgRNA expression. Puro can be used for screening, non-viral vector.	pU6:sgRNA	Amp	Puro/Fluc	Inquiry
Em18		CRISPR-AsCas12a All-in-one vector. The EF1a promoter initiates AsCpf1 (AsCas12a) expression, and the U6 promoter initiates crRNA (gScaffold-gRNA) expression. Lentivirus packaging can be performed.	pEF1α:AsCpf1/Puro-pU6:crRNA	Amp	N/A	Inquiry
Em19		The cytosine base editor CBE3, U6 promoter initiates sgRNA expression, and the EF-1α promoter initiates BE3 expression (including APOBEC-1 / nCas9 (D10A) / UGI). The C corresponding to the 4-8 base of the sgRNA sequence is the target mutation base. Lentivirus packaging can be performed.	pU6:sgRNA-pEF-1α:APOBEC-1/nCas9/UGI	Amp	Puro	Inquiry
Em20		The cytosine base editor CBE4, U6 promoter initiates sgRNA expression, and the EF-1α promoter initiates BE4 expression (including APOBEC-1 / nCas9 (D10A) / 2 * UGI). The C corresponding to the 4-8 base of the sgRNA sequence is the target mutation base. Lentivirus packaging can be performed.	pU6:sgRNA-pEF-1α:APOBEC-1/nCas9/2*UGI	Amp	Puro	Inquiry
Em21		Adenine base editor ABE. The CMV promoter initiates the expression of ABE7.10 (TadA-linker-Tad * A (7.10) -linker-nCas9). The editing efficiency in human cells is about 50 % by editing the 4-9th position of the sgRNA sequence. No sgRNA insertion site, non-viral vector.	pCMV:ABE7.10	Amp	N/A	Inquiry
Em22		Adenine base editor ABE. The U6 promoter initiates sgRNA expression, and the CAG promoter initiates ABE7.10 / St1Cas9 expression. The 4-9 A of sgRNA sequence is edited, and the editing efficiency in human cells is about 50%. Non-viral vector.	pU6:sgRNA-pCAG:ABE7.10/St1Cas9	Amp	N/A	Inquiry
Epara01	Arabidopsis Thaliana	All-in-one vector. The 35S promoter initiates Cas9 expression, and the At U6-26 promoter initiates sgRNA expression. Hygro screening can be performed.	35s:Cas9-AtU6-26:sgRNA	Kan	Hygro	Inquiry
Epri01	Rice	All-in-one vector. The rice snoRNA U3 promoter initiates sgRNA expression, and the UBI promoter initiates Cas9 expression. Hygro screening can be performed.	rice snoRNA U3 promoter :sgRNA- pUBI:Cas9	Kan	Hygro	Inquiry
Ee01	E. coli	sgRNA vector. It is used for gene knockdown in bacteria, together with the Cas9 vector and donor template DNA.	J23119（SpeI）:sgRNA	Amp	N/A	Inquiry
Ee02		sgRNA vector. It is used for gene knockdown in bacteria, together with the Cas9 vector and donor template DNA.	J23119（SpeI）:sgRNA	Spec	N/A	Inquiry
Ee03		spCas9 vector. Tetracycline-induced spCas9 expression is used for gene knockdown in bacteria. Co-used with Cas9 vector and Donor template DNA.	pLtetO-1:SpCas9	Amp	N/A	Inquiry
Enem01	Nematodes	sgRNA vector. U6 promoter initiates sgRNA expression.	pU6:sgRNA-DHFR	Amp	DHFR	Inquiry
Enem02		sgRNA vector. The T7 promoter initiates in vitro transcription of sgRNA to obtain sgRNA.	pT7:sgRNA	Kan	Neo	Inquiry
Enem03		All-in-one vector. The U6 promoter initiates sgRNA expression, and pTgTUB1 initiates Cas9 expression.	pU6:sgRNA-pTgTUB1:Cas9	Amp	N/A	Inquiry
Enem04		Cas9 vector. The TgTUB1 promoter initiates Cas9 expression.	pTgTUB1:Cas9	Amp	CAT	Inquiry
Ezeb01	Zebrafish	Cas9 vector. Non-viral vector.	pCMV-pT7:Cas9/3*Flag	Amp	3*Flag	Inquiry
Ezeb02		sgRNA vector. The gRNA is obtained by in vitro transcription under the T7 promoter.	pT7:sgRNA	Kan	N/A	Inquiry
Ezeb03		All-in-one vector, tissue-specific knockout vector, double sgRNA vector, non-viral vector.	pUAS:Cas9-pU6:sgRNA1;pU6:sgRNA2	Amp	Cre	Inquiry
Edro01	Drosophila melanogaster	All-in-one vector, non-viral vector. dU6-2 initiates sgRNA expression, and Ac5 promoter initiates Cas9 expression. Puro can be used for screening.	pdU6-2:sgRNA-pAc5:Cas9	Amp	Puro	Inquiry
Edro02		sgRNA vector. dU6-2 initiates sgRNA expression, and Ac5 promoter initiates EGFP and Puro expression. EGFP and Puro can be used for screening.	pdU6-2:sgRNA-pAc5:EGFP/Puro	Amp	Puro/EGFP	Inquiry
Edro03		Cas9 vector. MT promoter initiates Cas9 expression. Screening with Hygro.	pMT:Cas9	Amp	Hygro	Inquiry
Esa01	Saccharomyces cerevisiae	All-in-one vector. The promoter ROX3 initiates spCas9 expression, and the promoter SNR52 initiates sgRNA expression. Neo / G418 can be used for screening.	pROX3:Cas9-pSNR52:sgRNA	Amp	Neo/G418	Inquiry

QUOTE

Intellectual Property Rights StatementView More

Synbio Technologies designs and manufactures nucleic acid vectors based on customer’s requirements. While we participate in the design and manufacturing of these vectors, it does not imply that we possess any intellectual property rights over them or the right to transfer such intellectual property rights, unless otherwise agreed upon by both parties.

The customer understands and agrees that the use of the vectors designed and ordered by the customer, as well as the related vector components, is solely at the discretion and responsibility of the customer. When purchasing products and services from Synbio Technologies, the customer should be fully aware that they may need to obtain licenses or authorizations from relevant third-party intellectual property owners. Any disputes or claims arising from the customer's purchase of products or use of services that may be related to third-party intellectual property rights shall be solely the responsibility of the customer, and Synbio Technologies shall not bear any responsibility for them.

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