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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:
Interest directly into this itr-containing vector. express both the recombinant protein and vitality hrgfp reporter from same mrna transcript.
Description:
SureVector Yeast N-terminal Expansion, include functional modules only (no assembly reagents/competent cells), used to create yeast expression vectors and provides guidelines on selecting module to include in assembly mixture, Size: 15 cloning reactions
Description:
A protease-deficient E. coli host strain for optimal expression of recombinant proteins.High-level expression of a variety of recombinant proteins.Defective in E. coli strain B, and wild-type restriction systems to permit high efficiency transformation with unmodified plasmid DNA.
Description:
SureVector Yeast C-terminal Expansion, include functional modules only (no assembly reagents or competent cells), used to create yeast expression vectors and provides guidelines on selecting module to include in assembly mixture, Size: 15 cloning rxns
Description:
PETDuet-1 is designed for the coexpression of two target genes. The vector encodes two multiple cloning sites (MCS), each of which is preceded by a T7 promoter, lac operator and ribosome binding site (rbs), HisTag, STag, Duet pET bacterial prokaryotic, ≤ -70degreeC
Description:
PET-21a-d(+) vectors carry an N-terminal T7Tag* sequence plus an optional C-terminal HisTag* sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
SiRNA Cloning Vector (pGB), contain the human U6 RNA polymerase III promoter, neomycin/kanamycin-resistance gene and 2 unique restriction sites, BamH I and Xba, Storage: -20 degree C, Application: Transfected into mammalian cells using Lipofectamine (Invitrogen), Size: 20ug
Description:
The pET-28a-c(+) vectors carry an N-terminal HisTag*/thrombin/T7Tag* configuration plus an optional C-terminal HisTag sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
The pET-23a-d(+) vectors carry an N-terminal T7Tag* sequence plus an optional C-terminal HisTag* sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
The pET-28a-c(+) vectors carry an N-terminal HisTag*/thrombin/T7Tag* configuration plus an optional C-terminal HisTag sequence, The pET Vectors are supplied as purified plasmid DNA, Storage ≤ -70degreeC
Description:
Store competent cells at -70[degree]C; store all other components at -20[degree]C. pGEM-T Easy Vector Systems I and II are guaranteed for at least 6 months from the date of purchase when stored and handled properly.
Description:
Store competent cells at -70[degree]C; store all other components at -20[degree]C. pGEM-T Vector Systems I and II are guaranteed for at least 6 months from date of purchase, when stored and handled properly.
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:
PGL4.52[Luc2P/Stat5Re/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:
Store at -20[degree]C. The pCI-neo Mammalian Expression Vector is selectable for studying constitutive expression of genes in mammalian cells.
Description:
Store vector at -20[degree]C. The pSP64 Poly(A) Vector can be used as a standard cloning vector and also can be used for in vitro transcription from the SP6 promoter. The pSP64 Poly(A) Vector can be used to generate poly(A)+ transcripts in vitro.
Description:
PGL4.19(Luc2Cp/Neo) 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:
Store vector DNA at -20[degree]C. Store glycerol stock of JM109 at -70[degree]C. The pRL family of Renilla luciferase (Rluc) control reporter vectors is designed for use with the Dual-Luciferase; Reporter Assay System.
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:
PGL4.18(Luc2P/Neo) 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:
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:
PGL4.82(Hrluc/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.
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