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Vectors, Plasmids and Libraries
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Vectors, Plasmids and Libraries
404 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:
Plive Vector/Seap Control, designed for high and prolonged expression of transgenes in the mouse liver. Expression of the SEAP (Secreted Embryonic Alkaline Phosphatase) gene from pLIVE-SEAP can be easily monitored using a quantitative assay of mouse serum, Size: 20ug
Description:
PFN21A Halotag Cmv Flexi Vector, designed for expression of N-terminal-tagged HaloTag* fusion proteins in mammalian cells, for cell imaging of protein localization or trafficking in conjunction with the fluorescent HaloTag* Ligands,, Size: 20ug
Description:
PF3K Wg (Bydv) Flexi 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:
PGL4.83(Hrlucp/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:
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:
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:
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.
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:
PNLF1-HIF1A [CMV/neo] Vector, HIF1A Vector System enables simple quantification of intracellular HIF1A protein, contains a vector encoding NanoLuc* fused to the C-terminus of the HIF1A protein, Application: Hypoxia signaling, Compound screening, Storage: -20 deg C, size: 5 x 20 ug
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:
PGL4.21(Luc2P/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
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