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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:
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:
Contains a multiple cloning region for convenient cloning and a His6HaloTag* protein coding region that allows for both purification and labeling of the expressed fusion protein.
Description:
Provides constitutive high-level protein expression in mammalian cells using the human cytomegalovirus (CMV) immediate early enhancer/promoter. The vector contains a multiple cloning region for convenient cloning, and can be used for both transient and stable gene expression.
Description:
Store competent cells at -70[degree]C; store all other components at -20[degree]C. The pTARGET; Systems is guaranteed for at least 6 months from the date of purchase when stored and handled properly.
Description:
HaloTag* Flexi* Vector, CMV Deletion Series Sample Pack, Versatility, Time Savings, Enhanced Productivity, Easy Access, for expression of C-terminal-tagged HaloTag* fusion proteins in mammalian cells, for cell imaging of protein localization or trafficking in conjunction, size : 9 x 2ug
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:
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:
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:
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:
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
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