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安全信息

E7408

Sigma-Aldrich

p3XFLAG-CMV-7 Expression Vector

shuttle vector for transient expression of N-terminal Met-3xFLAG

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About This Item

UNSPSC代码:
12352200

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标签

Met-3X FLAG tagged

等级

Molecular Biology

表单

buffered aqueous solution

肽标签位置

N-terminal

运输

dry ice

储存温度

−20°C

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OGS633OGS636OGS635
origin of replication

pUC

origin of replication

pUC

origin of replication

pUC

origin of replication

pUC

peptide tag location

N-terminal

peptide tag location

N-terminal

peptide tag location

N-terminal

peptide tag location

C-terminal

bacteria selection

ampicillin

bacteria selection

ampicillin

bacteria selection

ampicillin

bacteria selection

ampicillin

peptide cleavage

EKT

peptide cleavage

EKT

peptide cleavage

EKT

peptide cleavage

EKT

mol wt

size 5477 bp

mol wt

size 5534 bp

mol wt

size 5496 bp

mol wt

size 5502 bp

一般描述

p3XFLAG-CMV-7 Expression Vector is a 4.7 kb derivative of pCMV5 used to establish expression of N-terminal Met-FLAG® fusion proteins in mammalian cells. The vector encodes the ANTI-FLAG M2 antibody epitope (Asp-Tyr-Lys-Xaa-Xaa-Asp) three times, upstream of the multiple cloning region. This results in increased detection sensitivity using ANTI-FLAG M2. The third epitope includes the enterokinase recognition sequence allowing cleavage of the 3XFLAG peptide from the purified fusion protein. Efficiency of replication is optimal when using an SV40 T antigen-expressing host.

p3XFLAG-CMV-7-BAP Control Plasmid is a 6.2 kb derivative of pCMV5 used for transient intracellular expression of N-terminal 3XFLAG bacterial alkaline phosphatase fusion protein in mammalian cells. The vector encodes three adjacent FLAG epitopes (Asp- Tyr-Lys-Xaa-Xaa-Asp) upstream of the multiple cloning region. This results in increased detection sensitivity using ANTI-FLAG M2 antibody.3 The third FLAG epitope includes the enterokinase recognition sequence, allowing cleavage of the 3XFLAG peptide from the purified fusion protein.

Vector Maps and Sequences

组分

  • p3XFLAG-CMV-7 Expression Vector 20 μg (E2400) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.
  • p3XFLAG-CMV-7-BAP Control Plasmid 20 μg (C7472) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.

原理

The promoter-regulatory region of the human cytomegalovirus drives transcription of FLAG®-fusion constructs. p3XFLAG-CMV-7 Expression Vector is a shuttle vector for E. coli and mammalian cells.

法律信息

This product is covered by the following patents owned by Sigma-Aldrich Co. LLC: US6,379,903, US7,094,548, JP4405125,EP1220933, CA2386471 and AU774216.
FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
p3xFLAG-CMV is a trademark of Sigma-Aldrich Co. LLC

储存分类代码

10 - Combustible liquids

法规信息

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    Zaruhi Karabekian et al.
    Journal of virology, 79(6), 3525-3535 (2005-02-26)
    The murine cytomegalovirus (MCMV) proteins encoded by US22 genes M139, M140, and M141 function, at least in part, to regulate replication of this virus in macrophages. Mutant MCMV having one or more of these genes deleted replicates poorly in macrophages
    Tatsuo Kido et al.
    International journal of cancer, 123(7), 1573-1585 (2008-07-24)
    Testis-specific protein Y-encoded (TSPY) is the putative gene for the gonadoblastoma locus on the Y chromosome. TSPY is expressed in normal germ cells of fetal and adult testis and ectopically in tumor germ cells, including gonadoblastoma in intersex patients, testicular
    Pou5f1 contributes to dorsoventral patterning by positive regulation of vox and modulation of fgf8a expression.
    Belting, H.-G., et al.
    Developmental Biology, 256, 323-323 (2011)
    Linghua Qiu et al.
    Molecular neurodegeneration, 8, 1-1 (2013-01-04)
    A proline-to-serine substitution at position-56 (P56S) of vesicle-associated membrane protein-associated protein B (VAPB) causes a form of dominantly inherited motor neuron disease (MND), including typical and atypical amyotrophic lateral sclerosis (ALS) and a mild late-onset spinal muscular atrophy (SMA). VAPB
    Qi-Heng Yang et al.
    Genes & development, 17(12), 1487-1496 (2003-06-20)
    Omi/HtrA2 is a mitochondrial serine protease that is released into the cytosol during apoptosis to antagonize inhibitors of apoptosis (IAPs) and contribute to caspase-independent cell death. Here, we demonstrate that Omi/HtrA2 directly cleaves various IAPs in vitro, and the cleavage

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