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E8408

Sigma-Aldrich

pFLAG-CTC Expression Vector

Bacterial vector for cytoplasmic expression of C-terminal FLAG fusion proteins

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About This Item

UNSPSC Code:
12352200

Pricing and availability is not currently available.

tag

FLAG® tagged

grade

Molecular Biology
for molecular biology

form

buffered aqueous solution

shipped in

dry ice

storage temp.

−20°C

General description

The pFLAG-CTC Expression Vector is a 5.3 kb E. coli expression vector used for cytoplasmic expression of a properly inserted open reading frame as a C-terminal FLAG® fusion protein. 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.

C-terminal FLAG fusion proteins may be purified using Monoclonal ANTI-FLAG M2, Catalog Number F3165, and ANTI-FLAG M2 Affinity Gel, Catalog Number A2220.

The pFLAG-CTS-BAP Control Plasmid is a 6.7 kb vE. coli plasmid used for efficient and controlled periplasmic expression of C-terminal FLAG-BAP fusion protein.

Vector Maps and Sequences

Components

  • pFLAG-CTC Expression Vector 10 μg (E5394) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.
  • pFLAG-CTS-BAP Control Plasmid 1 μg (P7707) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.

Principle

The promoter-regulatory region of the strong tac promoter (a hybrid of the trp and lac promoters from E.coli) drives transcription of ORF-FLAG fusion constructs. Control of transcription is regulated by the presence of the lacO sequences and inclusion of the lac repressor gene (lacI) on the plasmid.

Legal Information

FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
pFLAG-CTC is a trademark of Sigma-Aldrich Co. LLC
pFLAG-CTS is a trademark of Sigma-Aldrich Co. LLC

Storage Class Code

10 - Combustible liquids

Regulatory Information

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    M W Jackson et al.
    FEMS microbiology letters, 186(1), 85-90 (2000-04-26)
    Interactions among the Yersinia secretion (Ysc) proteins of Yersinia pestis were explored using the yeast two-hybrid system. Various pairwise combinations of the yscEFGHIKLN and Q genes fused to the DNA-binding or activation domain of the yeast GAL4 gene were introduced
    Ram P Garg et al.
    Proceedings of the National Academy of Sciences of the United States of America, 105(18), 6543-6547 (2008-05-03)
    The antibiotic valanimycin is a naturally occurring azoxy compound produced by Streptomyces viridifaciens MG456-hF10. Precursor incorporation experiments showed that valanimycin is derived from l-valine and l-serine via the intermediacy of isobutylamine and isobutylhydroxylamine. Enzymatic and genetic investigations led to the
    Chang-Sik Oh et al.
    Plant physiology, 145(2), 426-436 (2007-08-21)
    HrpN (harpin) protein is critical to the virulence of the fire blight pathogen Erwinia amylovora in host plants like apple (Malus x domestica). Moreover, exogenous treatment of Arabidopsis (Arabidopsis thaliana), a nonhost plant, with partially purified HrpN enhances growth. To
    Chlamydia trachomatis Secretion of an Immunodominant Hypothetical Protein (CT795) into Host Cell Cytoplasm
    Manli Qi, Lei Lei, Siqi Gong, Quanzhong Liu, et al
    Journal of Bacteriology, 193, 24698-22509 (2011)
    K A Mookhtiar et al.
    Diabetes, 45(12), 1670-1677 (1996-12-01)
    Glucokinase is a critical component of the physiological glucose sensor found in cell types that are responsive to changes in plasma glucose levels. The acute regulation of glucokinase activity has been shown to occur via a regulatory protein found in

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