pPICZα A载体说明书

 

pPICZα A

型号 载体名称 出品公司 载体用途
VJI0296 pPICZα A Invitrogen 酵母表达载体

 

5´ AOX1 promoter region: bases 1-941

5´ AOX1 priming site: bases 855-875

α-factor signal sequence: bases 941-1207

Multiple cloning site: bases 1208-1276

c-myc epitope: bases 1275-1304

Polyhistidine (6xHis) tag: bases 1320-1337

3´ AOX1 priming site: bases 1423-1443

AOX1 transcription termination region: bases 1341-1682

TEF1 promoter: bases 1683-2093

EM7 promoter: bases 2095-2162

Sh ble ORF: bases 2163-2537

CYC1 transcription termination region: bases 2538-2855

pUC origin: bases 2866-3539 (complementary strand)

 

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pAAV-LacZ载体说明书

 

pAAV-LacZ

型号 载体名称 出品公司 载体用途
VXS0411 pAAV-LacZ Stratagene 腺相关病毒系统

Related Products

1. VPK-402: AAV Helper Free Packaging System 

2. AAV-100: 293AAV Cell Line 

3. VPK-140: ViraBind™ AAV Purification Kit 

4. VPK-141: ViraBind™ AAV Purification Mega Kit 

5. VPK-145: QuickTiter™ AAV Quantitation Kit 

6. AAV-200: ViraDuctin™ AAV Transduction Kit 

Safety Considerations

Remember that you will be working with samples containing infectious virus. Follow the 

recommended NIH guidelines for all materials containing BSL-2 organisms. The AAV Helper-Free 

system is designed to minimize the chance of generating wild type AAV, but precautions should still 

be taken to avoid direct contact with viral supernatants. 

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pSRE-Luc载体说明书


 pSRE-Luc

型号 载体名称 出品公司 载体用途
VXS0449 pSRE-Luc Stratagene 信号通路报告载体

Instruction Manual

Catalog #219073 (AP-1 cis-Reporting System) #219075 (CRE cis-Reporting System) 

#219077 (NF-κB cis-Reporting System) #219079 (SRE cis-Reporting System) 

#219081 (SRF cis-Reporting System) #219083 (p53 cis-Reporting System) 

#219092 (ISRE cis-Reporting System) #219093 (GAS cis-Reporting System) 

#219094 (NFAT cis-Reporting System) #219095 (TARE cis-Reporting System) 

#240111 (C/EBP cis-Reporting System) #240113 (DR1 cis-Reporting System) 

#240115 (DR3 cis-Reporting System) #240119 (DR5 cis-Reporting System) 

#240129 (Egr-1 cis-Reporting System) #240131 (LILRE cis-Reporting System) 

#240133 (GRE cis-Reporting System) #240135 (DR4 cis-Reporting System) 

#240049 (pAP-1-hrGFP Plasmid) #240050 (pCRE-hrGFP Plasmid) 

#240051 (pNF-κB-hrGFP Plasmid) #240053 (pNFAT-hrGFP Plasmid) 

#219087 (pLuc-MCS Plasmid) 

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pSI载体说明书


型号 载体名称 出品公司 载体用途 价格
VPP0044 pSI Promega 哺乳动物表达载体 800

载体描述: 

The pSI Mammalian Expression Vector promotes constitutive expression of cloned DNA inserts in mammalian cells. The major difference between the pCI and pSI Mammalian Expression Vectors is the enhancer/promoter region controlling the expression of the inserted gene. The pSI Expression Vector contains the simian virus 40 (SV40) enhancer and early promoter region. This vector can be used for both transient and stable expression of genes. For stable expression, the pSI Vector must be co-transfected with an expression vector containing a selectable gene for mammalian cells.

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pAdEasy-1载体

 

pAdEasy-1

型号 载体名称 出品公司 载体用途
VXS0387 pAdEasy-1 Stratagene 腺病毒系统
载体描述: 

Recombine plasmids from the shuttle vectors (pShuttle, pShuttle-CMV, pAdTrack, pAdTrack-CMV) into the adenoviral plasmid pAdEasy®-1.
Plasmids recombined in pAdEasy®-1 should be packaged in either 293 or 911 cells to make virus.

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pCMV-Tag 5B载体说明书


型号 载体名称 出品公司 载体用途 价格
VPS0545 pCMV-Tag 5B Stratagene 哺乳动物表达载体 800

 

产品参数: 

Key Function:Constitutive Expression
Mammalian Selection:Neo,G418
Promoter:CMV
Cloning Method:Restriction Enzyme/MCS
Constitutive or Inducible System:Constitutive

载体抗性: 

卡那霉素(Kanamycin)

载体描述: 

Epitope tags provide a method to localize gene products in living cells, identify associated proteins, track the movement of tagged proteins within a cell, and characterize new genes without creating protein-specific antibodies. The pCMV-Tag1 vector contains both the synthetic FLAG epitopell ll and the c-myc epitope from the human c-myc gene. The pCMV-Tag1 vector allows production of fusion proteins in a variety of conformations. The pCMV-Tag2-5 vectors allow either c-myc or FLAG epitope tagging at either the C- or N-terminus. Each pCMV-Tag2-5 vector is supplied with all three reading frames for easy cloning and expression. The small size of the FLAG (eight amino acids long) and c-myc epitope tags (ten amino acids long) decreases the possibility of interference with the tagged protein. The FLAG and c-myc epitopes are recognized by the anti-c-myc and anti-FLAG antibodies, which can be used to characterize the target protein. The pCMV-Tag vectors allow high-level expression of tagged proteins in mammalian cells. Expression is driven by the human cytomegalovirus (CMV) immediate early promoter. The CMV promoter provides constitutive expression of cloned genes in a wide variety of cell lines. The translational start sequence used in the pCMV-Tag1, pCMV-Tag2 and pCMV-Tag3 vectors is a 10-base Kozak consensus sequence of CGG(A/G)CCATGG. pCMV-Tag4 and pCMV-Tag5 vectors do not contain a translation start sequence. Stable clone selection is made possible with G418 by the presence of the neomycin-resistance gene. The pCMV-Tag vectors are only 4.3 kb, allowing easy cloning and vector manipulations. This small size is due to the single antibiotic selection marker used by both prokaryotic and mammalian cells. The neomycin-resistance gene provides stable selection in mammalian cells with G418 driven by the SV40 promoter and kanamycin selection in E. coli cells driven by the bla (ß-lactamase) promoter.

 

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pGRE-Luc载体说明书


 pGRE-Luc

型号 载体名称 出品公司 载体用途
VXC0430 pGRE-Luc Clontech 信号通路报告载体

 

Instruction Manual

Catalog #219073 (AP-1 cis-Reporting System) #219075 (CRE cis-Reporting System) 

#219077 (NF-κB cis-Reporting System) #219079 (SRE cis-Reporting System) 

#219081 (SRF cis-Reporting System) #219083 (p53 cis-Reporting System) 

#219092 (ISRE cis-Reporting System) #219093 (GAS cis-Reporting System) 

#219094 (NFAT cis-Reporting System) #219095 (TARE cis-Reporting System) 

#240111 (C/EBP cis-Reporting System) #240113 (DR1 cis-Reporting System) 

#240115 (DR3 cis-Reporting System) #240119 (DR5 cis-Reporting System) 

#240129 (Egr-1 cis-Reporting System) #240131 (LILRE cis-Reporting System) 

#240133 (GRE cis-Reporting System) #240135 (DR4 cis-Reporting System) 

#240049 (pAP-1-hrGFP Plasmid) #240050 (pCRE-hrGFP Plasmid) 

#240051 (pNF-κB-hrGFP Plasmid) #240053 (pNFAT-hrGFP Plasmid) 

#219087 (pLuc-MCS Plasmid)

 

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pQCXIH载体说明书


 pQCXIH载体说明书

型号 载体名称 出品公司 载体用途
VNC0418 pQCXIH Clontech 逆转录病毒载体

 

 

产品参数: 

Promotor: CMV/MSV
Size: 7800
5′ Sequencing 1 Primer: QC
5′ Sequencing 1 Primer Sequence: 5’d[ACGCCATCCACGCTGTTTTGACCT]3′
Tag 1: IRES-Hygro
Selectable Marker: Hygromycin
Viral/Non-Viral: Retroviral

载体抗性: 
氨苄青霉素(Ampicillin)
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pRetroX-IRES-ZsGreen1载体说明书

 Clontech逆转录病毒载体

pRetroX-IRES-ZsGreen1

型号 载体名称 出品公司 载体用途
VNC0591 pRetroX-IRES-ZsGreen1 Clontech 逆转录病毒载体

Description

pRetroX-IRES-ZsGreen1 is a bicistronic, fl uorescent, retroviral vector that allows both a gene 

of interest and the ZsGreen1 gene to be translated from a single bicistronic mRNA. pRetroXIRES-ZsGreen1 is designed for effi cient delivery and selection (by fl ow cytometry or other 

methods) of stably transduced mammalian cells expressing the ZsGreen1 fl uorescent protein 

and the protein of interest. This vector can be used to obtain stable cell lines without timeconsuming drug and clonal selection. ZsGreen1 is derived from the reef coral Zoanthus sp. 

green fl uorescent protein (ZsGreen) and is easily detected with standard FITC fi lter sets (1).

Bicistronic expression from this vector is facilitated by the encephalomyocarditis virus (EMCV) 

internal ribosome entry site (IRES). This IRES facilitates cap-independent translation from an 

internal start site at the IRES/ZsGreen1 junction (2). ZsGreen1 is a human codon optimized 

ZsGreen variant that encodes the brightest commercially available green fl uorescent protein 

(1). This retroviral vector is derived from the pMIN series of vectors (3, 4). These optimized 

vectors have the ability to produce high viral titers, express genes at high levels, and, due 

to the absence of retroviral coding sequences, exhibit improved safety profi les. The multiple 

cloning site (MCS) in pRetroX-IRES-ZsGreen1 is between the 5’ MMLV LTR and the IRES 

sequence. Genes cloned into the MCS are expressed as a bicistronic message transcribed 

from the 5’ LTR.

pRetroX-IRES-ZsGreen1 contains all of the necessary viral RNA processing elements; these 

include the 5’ and 3’ LTRs, the packaging signal (ψ), and the tRNA primer-binding site. For 

safety reasons, however, the vector lacks the structural genes (gag, pol, and env) necessary for 

retroviral particle formation and replication. pRetroX-IRES-ZsGreen1 contains a ColE1 origin 

of replication, and an E. coli Ampr

 gene for propagation and selection in bacteria.

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pSilencer 3.1-H1 hygro载体说明书

 

pSilencer 3.1-H1 hygro

型号 载体名称 出品公司 载体用途
VRA0340 pSilencer 3.1-H1 hygro Ambion RNAi载体
载体描述: 

The pSilencer vectors employ RNA polymerase III (pol III) promoters which generate large amounts of small RNA using relatively simple promoter and terminator sequences. They also include an antibiotic resistance gene that provides a mechanism to select for transfected cells that express the introduced DNA.

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