DNA Vectors
SignaGen Laboratories AAV-GFP AAV SEROTYPE 4 1 X30UL
AAV4-CMV-GFP is a pre-packaged rAAV in serotype 4 (with capsid from AAV serotype 4 and 2xITR from AAV serotype 2) which express EGFP under CMV promoter. Used as a control and ready to use format.
System Biosciences LLC PCDH-MSCV-MCS-EF1A-GFP CDNA
pCDH-MSCV-MCS-EF1α-GFP cDNA Dual Promoter Cloning and Expression Lentivector 10ug
ANTIBODY DESIGN LABS PADL-100 IPHAGEMID VECTOR
pADL™-100 is a phagemid vector designed for high levels of display on the filamentous bacteriophage M13 or equivalent. This vector contains a PelB leader sequence followed by a full-length copy of the gene III sequence and a double-SfiI cloning site to introduce foreign polypeptides on the N-terminal side of the gene III protein. Expression of the fusion is under the tight control of a lac promoter. The presence of a strong RBS, a proteolysis-resistant linker without tags and the absence of amber stop codon all contribute to maximize display on pIII.
System Biosciences LLC pLL-CMV-GFP-T2A-Puro (Lenti-Labeler™ plasmid), 10ug
pLL-CMV-GFP-T2A-Puro (Lenti-Labeler™ plasmid),
SignaGen Laboratories AAV-GFP (AAV SEROTYPE 9)
Unit Size: 1 x >30 µL (>1E+13 VG/mL.AAV9-GFP is a pre-packaged rAAV in serotype 9 (with capsid from AAV serotype 9a nd 2xITR from AAV serotype 2) which over-expresses EGFP under CMV promoter. Ready to use format.
Invivogen Human IgG1 | 20ug
pFUSE-CHIg-hG1 is a cloning plasmid that expresses the constant region of the human IgG1 heavy chain. It contains a multiple cloning site upstream of the constant region to enable cloning of the heavy chain (CH) variable region. This plasmid is designed for antibody generation when co-transfected into mammalian cells with the light chain variable region cloned into pFUSE-CLIg. pFUSEss-CHIg-hG1 additionally features the IL2 signal sequence to allow the secretion of recombinant antibodies generated using fragment antigen-binding (Fab) or single-chain variable fragment (scFv) fragments selected from phage display libraries that lack a signal sequence.
Vector Biolabs The Adenovirus Co AD(RGD)-CMV-GFP
Ad infection is initiated by recognition of the native Ad5 receptor, coxsackievirus-adenovirus receptor (CAR), on target cells by the carboxy-terminal portion (i.e., knob) of the fiber protein. Therefore the infection efficiency of adenovirus is very low for cells with low or no CAR receptors. Arg-Gly-Asp (RGD) motif was introduced in the surface-exposed loops of adenovirus fiber knob, this enables the adenovirus to bypass CAR and mediate cell entry via RGD binding integrins. So the RDG modified adenovirus can be used for "retargeting" cells that regular adenovirus doesn't work well. The infection effeciency of RDG modified adenovirus can be tens or hundreds of times higher than standard Ad5 in some cells, including human or mouse macrophages, T cells, synoviocytes, islet grafts, adipocytes, MEF, etc.This is a RGD modified replication-deficient adenovirus expressing eGFP under a CMV promoter.
Clontech Labs 3P T-Vector pMD 20, 1 ug
pMD20 and pMD19 (Simple) T-Vectors are linearized PCR cloning vectors (cleaved by EcoRV) with single 3'-terminal thymidine residues (dT) at both ends. These T-overhangs at the cloning site improve the efficiency of ligation of PCR products that contain dA-overhangs. The inclusion of lacZ in these vectors allows blue/white screening for the detection of successful ligations.