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Vectors, Plasmids and Libraries
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Vectors, Plasmids and Libraries
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In molecular cloning, vectors are DNA molecules used to artificially deliver foreign genetic material into another cell. The four major types of vectors are plasmids, viral vectors, cosmids, and artificial chromosomes, with the most commonly used of these being plasmids. Vectors may be used for cloning, and certain vectors are specifically tailored to that exact purpose, while others may be designed specifically for transcription and protein expression. Simpler transcription vectors are used to amplify their inserted genetic material.
Description:
PETDuet-1 is designed for the coexpression of two target genes. The vector encodes two multiple cloning sites (MCS), each of which is preceded by a T7 promoter, lac operator and ribosome binding site (rbs), HisTag, STag, Duet pET bacterial prokaryotic, ≤ -70degreeC
Description:
PET-21a-d(+) vectors carry an N-terminal T7Tag* sequence plus an optional C-terminal HisTag* sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
The pET-28a-c(+) vectors carry an N-terminal HisTag*/thrombin/T7Tag* configuration plus an optional C-terminal HisTag sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
SiRNA Cloning Vector (pGB), contain the human U6 RNA polymerase III promoter, neomycin/kanamycin-resistance gene and 2 unique restriction sites, BamH I and Xba, Storage: -20 degree C, Application: Transfected into mammalian cells using Lipofectamine (Invitrogen), Size: 20ug
Description:
The pET-28a-c(+) vectors carry an N-terminal HisTag*/thrombin/T7Tag* configuration plus an optional C-terminal HisTag sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
The pET-23a-d(+) vectors carry an N-terminal T7Tag* sequence plus an optional C-terminal HisTag* sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
PGL4.32[Luc2P/Nf-Kb-Re/Hygro] Vector, Signaling Pathway Analysis (Minimal Promoter-Driven) Firefly Luciferase, Optimized For Expression In Mammalian Cells, report the activity of a variety of pathways using the optimized luc2 firefly luciferase gene in the PGL4 backbone, size: 20ug
Description:
Store at -20[degree]C. The pAdVAntage; Vector contains the Adenovirus Virus-associated I (VAI) RNA gene insert. This gene has been shown to increase expression of proteins by enhancing translation.
Description:
Contains a mimimal promoter, response elements and mimimal promoter. Promoter-containing vectors that can be used as expression controls or as co-reporter vectors.
Description:
PBIND-ERα Vector, Nuclear Receptor Analysis Luciferase, can be performed with traditional means by using a minimal promoter vector with nuclear receptor response elements upstream, Robust, More Sensitive, Adaptable, Consistent, Faster Results, size: 20ug
Description:
PF3A Wg (Bydv) Flexi(R) Vector, simple, yet powerful, directional cloning method for protein-coding sequences, based on two rare-cutting restriction enzymes, SgfI and PmeI, and provides a rapid, efficient and high-fidelity way to transfer protein-coding regions, Size: 20ug
Description:
Provides constitutive high-level protein expression in mammalian cells using the human cytomegalovirus (CMV) immediate early enhancer/promoter. The vector can be used for both transient and stable gene expression.
Description:
Is configured to append the His6HaloTag* tag to the carboxyterminus of the protein fusion partner and provides T7 RNA polymerase-driven protein expression in E. coli.
Description:
Contains a mimimal promoter, response elements and mimimal promoter. Promoter-containing vectors that can be used as expression controls or as co-reporter vectors.
Description:
Store competent cells at -70[degree]C; store all other components at -20[degree]C. pGEM-T Easy Vector Systems I and II are guaranteed for at least 6 months from the date of purchase when stored and handled properly.
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