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Merck
CN

E7283

p3XFLAG-myc-CMV-26 Expression Vector

shuttle vector for transient or stable intracellular dual tagged expression of N-terminal 3xFLAG and C-term c-myc

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UNSPSC Code:
12352200
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Product Name

p3XFLAG-myc-CMV-26 Expression Vector, shuttle vector for transient or stable intracellular dual tagged expression of N-terminal 3xFLAG and C-term c-myc

tag

3X FLAG tagged (N-terminal)
c-Myc tagged (C-terminal)

grade

Molecular Biology

form

buffered aqueous solution

shipped in

dry ice

storage temp.

−20°C

Biochem/physiol Actions

The promoter-regulatory region of the human cytomegalovirus drives transcription of FLAG® and c-myc fusion constructs. The aminoglycoside phosphotransferase II gene (Neo-r) confers resistance to aminoglycosides such as G 418 allowing for selection of stable transfectants.

General description

The p3XFLAG-Myc-CMV -26 Expression Vector is a 6.3 kb derivative of pCMV5 used to establish transient or stable intracellular expression of dual tagged N-terminal 3XFLAG and C-terminal c-myc fusion proteins in mammalian cells. The vector encodes three adjacent FLAG epitopes (Asp-Tyr-Lys-Xaa-Xaa-Asp) and a c-myc epitope (EQKLISEEDL) upstream and downstream of the multiple cloning sites, respectively. The third FLAG epitope includes the enterokinase recognition sequence, allowing cleavage of the 3XFLAG peptide from the purified fusion protein. The incorporation of 3XFLAG in the expression vector results in increased detection sensitivity using ANTI-FLAG M2 antibody. Efficiency of replication is optimal when using an SV40 T antigen expressing host.

The p3XFLAG-CMV-7-BAP Control Plasmid is a 6.2 kb derivative of pCMV5 used for transient intracellular expression of N-terminal 3X-FLAG 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. The third FLAG epitope includes the enterokinase recognition sequence, allowing cleavage of the 3XFLAG peptide from the purified fusion protein.

Vector Maps and Sequences

Legal Information

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
p3xFLAG-Myc-CMV is a trademark of Sigma-Aldrich Co. LLC

Other Notes

  • p3XFLAG-myc-CMV-26 Expression Vector 20 μg (E6401) 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.

Storage Class

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Regulatory Information

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Tania R Lizarbe et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 22(9), 3207-3215 (2008-05-23)
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Journal of virology, 78(22), 12566-12575 (2004-10-28)
The viral genome of Kaposi's sarcoma-associated herpesvirus (KSHV) persists as an extrachromosomal plasmid in latently infected cells. The KSHV latency-associated nuclear antigen (LANA) stimulates plasmid maintenance and DNA replication by binding to an approximately 150-bp region within the viral terminal
Patrick Lorès et al.
The FEBS journal, 277(6), 1453-1464 (2010-02-13)
The SWI/SNF chromatin remodelling complexes are important regulators of transcription; they consist of large multisubunit assemblies containing either Brm or Brg1 as the catalytic ATPase subunit and a variable subset of approximately 10 Brg/Brm-associated factors (BAF). Among these factors, BAF60
Hongbo Fang et al.
PloS one, 8(7), e69600-e69600 (2013-07-31)
Breast cancer occur both in hereditary and sporadic forms, and the later one comprises an overwhelming majority of breast cancer cases among women. Numerical and structural alterations involving chromosome 8, with loss of short arm (8p) and gain of long
Heena Dey et al.
BMC cell biology, 13, 27-27 (2012-11-01)
We previously demonstrated that p68 phosphorylation at threonine residues correlates with cancer cell apoptosis under the treatments of TNF-α and TRAIL (Yang, L. Mol Cancer Res Vol 3, pp 355-63 2005). In this report, we characterized the role of p68

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Instructions

p3xFLAG-Myc-CMV-25 and p3xFLAG-Myc-CMV-26 Vector Maps

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