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Merck
모든 사진(2)

주요 문서

E7158

Sigma-Aldrich

pFLAG-CMV-4 Expression Vector

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

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About This Item

UNSPSC 코드:
12352200

태그

Met-FLAG tagged

Grade

for molecular biology

형태

buffered aqueous solution

펩타이드 태그 위치

N-terminal

배송 상태

dry ice

저장 온도

−20°C

일반 설명

pFLAG-CMV-4 is a 6.2 kb expression vector used for transient or stable expression in mammalian cells. The vector is a derivative of pCMV5 used for transient or stable expression of a properly inserted open reading frame as an N-terminal Met-FLAG® fusion protein.

The pFLAG-CMV-4 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 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 for Sigma Aldrich.

pFLAG-CMV-4-BAP Control Plasmid is a 7.7 kb derivative of pCMV5 used for transient intracellular expression of N-terminal Met-FLAG bacterial alkaline phosphatase fusion protein in mammalian cells.

Vector Maps and Sequences

성분

  • pFLAG-CMV-4 Expression Vector 20 μg (E1775) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.
  • pFLAG-CMV-4-BAP Control Plasmid 20 μg (C4722) is supplied as 0.5 mg/ml in 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.

원리

The promoter-regulatory region of the human cytomegalovirus2 drives transcription of FLAG®-fusion constructs. The aminoglycoside phosphotransferase II gene (neo-r) confers resistance to aminoglycosides such as G 418 allowing for selection of stable transfectants.

법적 정보

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

관련 제품

제품 번호
설명
가격

Storage Class Code

10 - Combustible liquids


시험 성적서(COA)

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문서 라이브러리 방문

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M G Chaitra et al.
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Molecular cancer, 11, 88-88 (2012-12-12)
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Huang, Y., et al.
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