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Vectors, Plasmids and Libraries
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Vectors, Plasmids and Libraries
402 results were found
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:
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:
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 at -20[degree]C. The pSV- b-Galactosidase Control Vector is a positive control vector for monitoring transfection efficiencies of mammalian cells.
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:
Plive Vector/Lacz Control, designed for high and prolonged expression of transgenes in the mouse liver. Expression of the LacZ gene from pLIVE-LacZ can be monitored in the liver using either X-gal staining quantitative Beta-galactosidase assays, Size: 20ug
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:
Is configured to append the His6HaloTag* tag to the aminoterminus of the protein fusion partner and provides T7 RNA polymerase-driven protein expression in E. coli.
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:
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:
PGL4.22(Luc2Cp/Puro)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:
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:
Vector offers synthetic firefly luciferase luc2 gene under the control of the strong constitutive CMV (cytomegalovirus) promoter. Vector demonstrates high expression levels in a variety of cell lines tested.
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