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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:
NanoBRET* PPI Starter System, provide the vectors required to create NanoLuc* Luciferase and HaloTag* protein fusions to target proteins, Features: Understand Real Biology, Monitor Changes, See Improved Assay Performance, Scale Your Assays, Storage: -30 deg C to -10 deg C,
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:
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:
PLIVE* Vector Complete System, designed for high and prolonged expression of transgenes in the mouse liver. In addition to the pLIVE Vector, pLIVE-LacZ (encoding Beta-galactosidase) and pLIVE-SEAP are provided as positive controls.
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:
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:
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
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.