Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : VET1237
| Cat. No. | VET1237 |
| Species | Bacterial |
| Tag | C-His,N-Strep |
| Source | Insect cell, Escherichia coli |
| Promoter | IE1, p10 |
| Selection | Ampicillin |
A: se pIExBac vectors are designed for cloning and high-level expression of proteins by transiently transfecting Spodoptera-derived insect cells or by generating baculovirus recombinants.
A: The pIEx/Bac-1 vectors are designed for cloning and high-level expression of proteins by transiently transfecting Spodoptera-derived insect cells or by generating baculovirus recombinants.
A: Late/very late expression in the baculovirus mode is driven by the strong p10 promoter.
A: The pIEx/Bac-1 vector carries an N-terminal Strep Tag II coding sequence followed by a recognition site for enterokinase.
A: The presence of two tags is ideal for dual purification strategies designed to isolate full-length fusion proteins.
A: Two “gentle elution" tags at both the N- and C-terminus is helpful for isolate full-length fusion proteins
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The dual-purpose pIEx/Bac vectors are designed for cloning and high-level expression of proteins.we can transiently transfect Spodoptera-derived insect cells or by generating baculovirus recombinants.
The multiple cloning region of pIEXBac-1 vector is followed by an optional C-terminal His•Tag coding sequence, which is a deal choice.
The pIEXBac-1 vector is ideal for dual purification strategies designed to isolate full-length fusion proteins.
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