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Merck
모든 사진(1)

주요 문서

A9469

Sigma-Aldrich

Monoclonal ANTI-FLAG® M2-Alkaline Phosphatase antibody produced in mouse

clone M2, purified immunoglobulin, buffered aqueous glycerol solution

동의어(들):

Monoclonal ANTI-FLAG® M2 antibody produced in mouse, Anti-ddddk, Anti-dykddddk

로그인조직 및 계약 가격 보기

크기 선택

0.2 MG
₩906,903
1 MG
₩1,856,841

₩906,903


예상 입고일2025년 8월 07일세부사항



크기 선택

보기 변경
0.2 MG
₩906,903
1 MG
₩1,856,841

About This Item

UNSPSC 코드:
41106514
NACRES:
NA.32

₩906,903


예상 입고일2025년 8월 07일세부사항


생물학적 소스

mouse

결합

alkaline phosphatase conjugate

항체 형태

purified immunoglobulin

항체 생산 유형

primary antibodies

클론

M2, monoclonal

양식

buffered aqueous glycerol solution

종 반응성

all

농도

~1 mg/mL

기술

indirect ELISA: 1:20,000

동형

IgG1

면역원 서열

DYKDDDDK

배송 상태

wet ice

저장 온도

−20°C

유전자 정보

human ... ALPL(249)

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Monoclonal ANTI-FLAG® M2-Alkaline Phosphatase is a purified IgG 1 mouse antibody covalently conjugated to calf intestinal alkaline phosphatase (AP). The antibody conjugate binds to FLAG® fusion proteins and will recognize the FLAG® epitope at any position in the fusion protein (N-terminal, Met-N-terminal, C-terminal or internal FLAG® peptides).

애플리케이션

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)
Monoclonal ANTI-FLAG® M2-Alkaline Phosphatase antibody produced in mouse has been used:
  • in direct tissue blot immunoassay of sweet orange petioles samples[1]
  • in screening internalization of delta opioid receptor[2]
  • for screening cell-free protein expression using ELISA[3]

물리적 형태

Solution in Tris buffered saline containing 50% glycerol plus stabilizer and preservative

법적 정보

ANTI-FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Beth A Rasala et al.
Plant biotechnology journal, 9(6), 674-683 (2011-05-04)
Microalgae have the potential to be a valuable biotechnological platform for the production of recombinant proteins. However, because of the complex regulatory network that tightly controls chloroplast gene expression, heterologous protein accumulation in a wild-type, photosynthetic-competent algal chloroplast remains low.
Seongjoon Kang et al.
Biology, 7(2) (2018-05-09)
Chlamydomonas reinhardtii (Chlamydomonas) strains that are toxic to mosquito larvae because they express chloroplast transgenes that are based on the mosquitocidal proteins of Bacillus thuringiensis subsp. israelensis (Bti) could be very useful in mosquito control. Chlamydomonas has several advantages for
Beth A Rasala et al.
PloS one, 7(8), e43349-e43349 (2012-09-01)
Microalgae have recently received attention as a potential low-cost host for the production of recombinant proteins and novel metabolites. However, a major obstacle to the development of algae as an industrial platform has been the poor expression of heterologous genes
Jiandong Chen et al.
Genes & development, 31(13), 1382-1395 (2017-08-11)
Mismatch repair (MMR) is a conserved mechanism exploited by cells to correct DNA replication errors both in growing cells and under nongrowing conditions. Hfq (host factor for RNA bacteriophage Qβ replication), a bacterial Lsm family RNA-binding protein, chaperones RNA-RNA interactions
Waithaka Mwangi et al.
Journal of leukocyte biology, 78(2), 401-411 (2005-04-29)
Induction of immune responses against microbial antigens using DNA is an attractive strategy to mimic the immunity induced by live vaccines. Although DNA vaccines are efficacious in murine models, the requirement for multiple immunizations using high doses in outbred animals

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