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Merck

E6783

pFLAG-CMV-3 Expression Vector

shuttle vector for transient or stable expression of N-terminal FLAG

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UNSPSC Code:
12352200
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Nazwa produktu

pFLAG-CMV-3 Expression Vector, shuttle vector for transient or stable expression of N-terminal FLAG

tag

FLAG® tagged

grade

Molecular Biology

form

buffered aqueous solution

peptide tag location

N-terminal

shipped in

dry ice

storage temp.

−20°C

Application

pFLAG-CMV-3 Expression Vector is suitable for transient or stable expression and secretion of N-terminal FLAG-tagged fusion proteins in mammalian cells.

Biochem/physiol Actions

The promoter-regulatory region of the human cytomegalovirus drives transcription of FLAG-fusion constructs. The preprotrypsin leader sequence precedes the FLAG® sequence and directs secretion of the fusion protein into the culture medium. The aminoglycoside phosphotransferase II gene (neo-r) confers resistance to aminoglycosides such as G 418, allowing for selection of stable transfectants.

General description

The pFLAG-CMV-3 Expression Vector is a 6.3 kb vector used for transient or stable expression in
mammalian cells. The vector is a derivative of pCMV5 used for transient or stable expression and secretion of a properly inserted open reading frame as an N-terminal FLAG fusion protein.

The pFLAG-CMV-3 Expression Vector is a shuttle vector containing both bacterial and SV40 origins of replication for propagation in both E. coli and mammalian cells. Efficiency of replication and genomic integration is optimal when using host cells that express the SV40 large T antigen.

The pFLAG-CMV-3-BAP Control Plasmid is a 7.7 kb derivative of pCMV51 used for transient expression and secretion of N-terminal FLAG bacterial alkaline phosphatase fusion protein in mammalian cells.

The FLAG® epitope is a small, hydrophilic 8 amino acid tag (DYKDDDDK) that provides for sensitive detection and high quality purification using ANTI-FLAG products available from Sigma-Aldrich.

Vector Maps and Sequences

Other Notes

  • pFLAG-CMV-3 Expression Vector 20 μg (E8770) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.
  • pFLAG-CMV-3-BAP Control Plasmid 20 μg (C3972) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.

Legal Information

FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
pFLAG-CMV is a trademark of Sigma-Aldrich Co. LLC
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Klasa składowania

10 - Combustible liquids


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

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Chenyun Wang et al.
Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 32(2), 299-302 (2012-04-25)
Many researchers employed mammalian expression system to artificially express cannabinoid receptors, but immunoblot data that directly prove efficient protein expression can hardly be seen in related research reports. In present study, we demonstrated cannabinoid receptor protein was not able to
Ahmet Sinan Sari et al.
Turkish journal of biology = Turk biyoloji dergisi, 45(3), 301-313 (2021-08-12)
Selective targeting of transfected mesenchymal stem cells (MSCs) carrying specific antioncogenes to the tumor was suggested as a treatment option. Bone morphogenetic protein-2 (BMP2) was shown to inhibit the proliferation and aggressiveness of osteosarcoma (OS) cells. Here, we aimed to
Raogo Ouedraogo et al.
Diabetes, 55(6), 1840-1846 (2006-05-30)
Adiponectin is an abundant adipocyte-derived plasma protein with antiatherosclerotic effects. Vascular signal transduction by adiponectin is poorly understood and may involve 5'-AMP-activated protein kinase (AMPK), cAMP signaling, and other pathways. Hyperglycemia sharply increases the production of reactive oxygen species (ROS)
Expression of human MDGA1 increases cell motility and cell-cell adhesion and reduces adhesion to extracellular matrix proteins in MDCK cells.
Diaz-Lopez, A., et al.
Cancer Microenvironment, 4, 23-23 (2011)
Jamila Gupte et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(6), 1508-1513 (2004-02-06)
The identification of endogenous or surrogate ligands for orphan G protein-coupled receptors (GPCRs) represents one of the most important tasks in GPCR biology and pharmacology. The challenge lies in choosing an appropriate assay in the absence of ways to activate

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Instructions

pFLAG-CMV-3 and pFLAG-CMV-4 Vector Maps

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