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Pcmv tag3b vector

Manufactured by Agilent Technologies
Sourced in Azerbaijan

The PCMV-Tag3B vector is a plasmid DNA vector designed for the expression of recombinant proteins in mammalian cells. It contains a cytomegalovirus (CMV) promoter for high-level expression, a polylinker region for inserting the gene of interest, and a C-terminal 3xFLAG tag for detection and purification of the expressed protein.

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2 protocols using pcmv tag3b vector

1

Subcellular Localization of Tulp Proteins

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Mouse Tulp1, Tulp2, Tulp3, and TUB cDNAs were cloned into the pIRES2-DsRed2 vector (Clontech plasmid #632420), which expresses both the gene of interest and the dsRed gene. TUB PIP2- and IFT-A-mutant cDNAs were cloned into the pLVX-EF1α-IRES-ZsGreen vector (Clontech plasmid #631982), which expresses both the gene of interest and the ZsGreen gene. To examine the subcellular localization of TULPs in RPE1 cells, mouse Tulp1, Tulp2, Tulp3, TUB, and Tulp1IFT-A(+) cDNAs were cloned into the pCMV-Tag3B vector (Agilent Technologies plasmid #211173), which makes it possible to visualize the expression of a gene of interest using an anti-Myc antibody.
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2

Galectin-1 and VEGF-Trap Protein Production

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Human LGALS1/Galectin-1 cDNA (GenBank No. NM_002305) was obtained from DNASU Plasmid Repository (Tempe, AZ) and subcloned into pCMV-Tag 3B vector (Agilent Technologies) with Myc tag and pGEX4T-2 vector (GE Healthcare, Piscataway, NJ) for glutathione S-transferase (GST) fusion. VEGF-TrapR1R2 (corresponding to aflibercept) cDNA16 (link) was generated as a synthetic gene by IDT (Coralville, IA), and subcloned into the pcDNA6.2/V5-DEST vector (Life Technologies) with V5 tag. The empty pcDNA6.2/V5-DEST vector was used as a Mock transfection control. The GST-fused galectin-1 protein was expressed in an Escherichia coli strain Rosetta-gami 2 (DE3) (Novagen, Madison, WI), and purified through binding to Glutathione Sepharose (GE Healthcare). All constructs were sequence-verified before use.
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