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Merck
CN

E8283

Sigma-Aldrich

pFLAG-CTS Expression Vector

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

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About This Item

UNSPSC代码:
12352200

标签

FLAG® tagged

等级

for molecular biology

表单

buffered aqueous solution

运输

dry ice

储存温度

−20°C

一般描述

The pFLAG-CTS 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 E. coli plasmid used for efficient and controlled periplasmic expression of C-terminal FLAG-BAP fusion protein.

Vector Maps and Sequences

应用

The pFLAG-CTS Expression Vector is suitable for cloning and expression of C-terminal FLAG® fusion proteins in E. coli.

组分

  • pFLAG-CTS Expression Vector 10 μg (E5269) 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.

原理

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.

法律信息

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

储存分类代码

12 - Non Combustible Liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

法规信息

常规特殊物品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Montarop Yamabhai et al.
Journal of biotechnology, 133(1), 50-57 (2007-10-24)
Bacillus spp. are Gram-positive bacteria that secrete a large number of extracellular proteins of industrial relevance. In this report, three Bacillus extracellular hydrolytic enzymes, i.e., alpha-amylase, mannanase and chitinase, were cloned and over-expressed in Gram-negative Escherichia coli. We found that
Parisa Asvadi et al.
Journal of molecular recognition : JMR, 15(5), 321-330 (2002-11-26)
In an attempt to generate recombinant anti-D reagents for possible diagnostic and therapeutic use we cloned the genes encoding the variable (V) domains of a human anti-D antibody secreted by the lymphoblastoid cell line BTSN4. A single-chain Fv (scFv) fragment
Jianzhi Zhang et al.
Proceedings of the National Academy of Sciences of the United States of America, 99(8), 5486-5491 (2002-03-28)
An improved understanding of the evolution of gene function at the molecular level may provide significant insights into the origin of biological novelty and adaptation. With the approach of ancestral protein reconstruction, we here address the question of how a
Chomphunuch Songsiriritthigul et al.
Microbial cell factories, 9, 20-20 (2010-04-13)
Mannans are one of the key polymers in hemicellulose, a major component of lignocellulose. The Mannan endo-1,4-beta-mannosidase or 1,4-beta-D-mannanase (EC 3.2.1.78), commonly named beta-mannanase, is an enzyme that can catalyze random hydrolysis of beta-1,4-mannosidic linkages in the main chain of
Jianzhi Zhang
Nature genetics, 38(7), 819-823 (2006-06-13)
Similar morphological or physiological changes occurring in multiple evolutionary lineages are not uncommon. Such parallel changes are believed to be adaptive, because a complex character is unlikely to originate more than once by chance. However, the occurrence of adaptive parallel

相关内容

Bacterial Expression Vectors: tac Promoter System

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