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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:
Store vector at -20[degree]C and host strain at -70[degree]C. The pGEM-3Z Vector can be used as a standard cloning vector and for in vitro transcription. The presence of the gene encoding the lacZ a-peptide allows recombinants to be selected using blue/white color screening. U.S.
Description:
PmirGLO Dual-Luciferase miRNA Target Expression Vector, designed to quantitatively evaluate microRNA (miRNA) activity by the insertion of miRNA target sites downstream or 3 of the firefly luciferase gene (luc2), primary reporter gene; reduced firefly luciferase expression, Size:20uG
Description:
PGL4.36[luc2P/MMTV/Hygro] 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:
PNLCoI2[luc2-P2A-NlucP/minP/Hygro] Vector, Coincidence Reporter Vector, For: Features: Improve Confidence and Save Time, Employ Robust and Sensitive Reporter Pair, Efficiently Identify False Hits, Use Simple Detection Format, Storage: -20 deg C, size: 20 ug
Description:
NanoLuc* (Nluc) luciferase (19.1kDa) enzyme. For luminescent reporting using furimazine to produce high intensity, glow-type luminescence. The luminescent reaction is ATP-independent and designed to suppress background luminescence for maximal assay sensitivity.
Description:
PGL4.39[Luc2P/Atf6 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:
PNLCoI4[luc2-P2A-NlucP/PGK/Hygro] Vector, Coincidence Reporter Vector, For: Features: Improve Confidence and Save Time, Employ Robust and Sensitive Reporter Pair, Efficiently Identify False Hits, Use Simple Detection Format, Storage: -20 deg C, size: 20 ug
Description:
NanoLuc* (Nluc) luciferase (19.1kDa) enzyme. For luminescent reporting using furimazine to produce high intensity, glow-type luminescence. The luminescent reaction is ATP-independent and designed to suppress background luminescence for maximal assay sensitivity.
Description:
PNLCoI1[luc2-P2A-NlucP/Hygro] Vector, Coincidence Reporter Vector, For: Features: Improve Confidence and Save Time, Employ Robust and Sensitive Reporter Pair, Efficiently Identify False Hits, Use Simple Detection Format, Storage: -20 deg C, size: 20 ug
Description:
NanoLuc* (Nluc) luciferase (19.1kDa) enzyme. For luminescent reporting using furimazine to produce high intensity, glow-type luminescence. The luminescent reaction is ATP-independent and designed to suppress background luminescence for maximal assay sensitivity.
Description:
PBIND-GR 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:
Store vector at -20[degree]C. The pSP72-pSP73 Vectors can be used as standard cloning vectors and can also be used for in vitro transcription from either strand using the SP6 or T7 promoter.
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