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Merck
CN

E0648

pcDNA 3.1 (−)/Myc−His C expression vector

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UNSPSC Code:
12352200
MDL number:
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grade

Molecular Biology

form

buffered aqueous solution

mol wt

5500 bp

storage temp.

−20°C

General description

pcDNA3.1 (-)/myc-his C is an expression vector that contains the strong CMV enhancer-promoter for high level expression of recombinant proteins in mammalian cells. The pcDNA3.1(-)/myc-his C expression vector contains a multiple cloning site (MCS) for easy cloning. pcDNA3.1(-) /myc-his C expression vector has a multiple cloning site in an opposite orientation from the pcDNA3.1(+). The vector is supplied in one of three reading frames to facilitate in frame cloning with a C-terminal tag containing a polyhistidine metal-binding region and the myc (c-myc) epitope.

The MCS has the following unique restriction sites: Apa I, Asp718 I, BamH I, BstX I, EcoR I, EcoR V, Hind III, KpN I, Nhe I, Not I, Pme I, Xba I, and Xho I. In addition, the SnaBI site in the CMV promoter is unique and the BstXI site in the MCS is redundant.

Application

pcDNA 3.1 (-)/Mys-His C Expression Vector is suitable for expression of recombinant proteins in mammalian cells.

Biochem/physiol Actions

The MCS, containing Apa I, Asp718 I, BamH I, BstX I, EcoR I, EcoR V, Hind III, KpN I, Nhe I, Not I, Pme I, Xba I, Xho I restriction sites, is in the reverse orientation. In addition, there is a unique SnaB I site in the CMV promoter.

Features and Benefits

  • CMV promoter/enhancer permits efficient, high-level expression
  • MCS facilitates easy insertion of your gene
  • Myc epitope allows recombinant protein detection
  • His-tag allows recombinant protein purification (on metal chelate resins)
  • Confers ampicillin resistance for selection of transformed bacteria
  • Confers neomycin resistance for selection of tranfected mammalian cells
  • SV40 promoter allows high level expression of inserted gene and episomal replication in cells expressing the large T antigen
A 5.5-kb vector for protein expression in mammalian cells. The vector incorporates both the myc epitope and polyHistidine in a C-terminal fusion protein tag. The A, B, and C versions differ in only a single base pair, allowing for translation in all possible reading frames.
All three contain the strong cytomegalovirus (CMV) enhancer-promoter sequence for high-level expression, the polyadenylation signal and transcription termination sequence from BGH to enhance mRNA stability, and the SV40 replication origin.

Other Notes

pcDNA 3.1 (-)/Mys-His C Expression Vector is supplied lyophilized in 10 mM Tris-HCl and 1 mM EDTA (pH 7.5).

存储类别

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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Christina Berube et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(40), 14314-14320 (2005-09-27)
The p53 tumor suppressor promotes cell cycle arrest or apoptosis in response to diverse stress stimuli. p53-mediated cell death depends in large part on transcriptional up-regulation of target genes. One of these targets, P53-induced protein with a death domain (PIDD)
Yang Xiang et al.
Cell research, 17(10), 850-857 (2007-10-10)
Histone methylation is an important epigenetic phenomenon that participates in a diverse array of cellular processes and has been found to be associated with cancer. Recent identification of several histone demethylases has proved that histone methylation is a reversible process.
Jie Liu et al.
Molecular medicine reports, 24(3) (2021-07-20)
Previous studies have identified microRNA (miRNA/miR)‑3613‑3p as a heat stress (HS)‑related miRNA in endothelial cells that can lead to apoptosis. However, the mechanism underlying the miR‑3613‑3p‑mediated apoptosis of HS‑exposed endothelial cells remains unclear. In the present study, western blot analysis

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