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Merck
모든 사진(1)

주요 문서

M3682

Sigma-Aldrich

Anti-MAP Kinase, Monophosphorylated Tyrosine antibody ,Mouse monoclonal

clone ERK-PY193, purified from hybridoma cell culture

동의어(들):

Anti-pY-ERK

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About This Item

MDL number:
UNSPSC 코드:
12352203
NACRES:
NA.43

생물학적 소스

mouse

Quality Level

결합

unconjugated

항체 형태

purified from hybridoma cell culture

항체 생산 유형

primary antibodies

클론

ERK-PY193, monoclonal

형태

buffered aqueous solution

분자량

antigen, ERK-1 44 kDa
antigen, ERK-2 42 kDa

종 반응성

rat, human

농도

~2 mg/mL

기술

capture ELISA: suitable
immunocytochemistry: suitable
microarray: suitable
western blot: 1-5 μg/mL using cell extract of rat fibroblasts cell line, Rat1, activated with sorbitol

동형

IgG1

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−20°C

타겟 번역 후 변형

phosphorylation (pTyr)

유전자 정보

관련 카테고리

일반 설명

Monoclonal Anti-MAP Kinase, Mono-phosphorylated Tyrosine (pY-ERK) (mouse IgG1 isotype) is derived from the ERK-PY193 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide sequence corresponding to the phosphorylated form of ERK-activation loop, conjugated to KLH. The mitogen-activated protein kinase (MAPK) superfamily of enzymes is involved in many signaling pathways. This family includes the ERK1/2 (extracellular signal-regulated protein kinase, also termed p42/p44 MAPK), JNK (c-Jun N-terminal protein kinase, also termed stress-activated protein kinase, SAPK1), and p38 MAPK (also termed SAPK2) subfamilies.

특이성

The antibody reacts with the monophosphorylated tyrosine form of MAP kinases (ERK1 and ERK2). It does not recognize the non-phosphorylated, diphosphorylated, and the monophosphorylated threonine forms of ERK/MAP kinases, or the diphosphorylated forms of JNK and p38 MAPK. The epitope recognized by the antibody contains the phosphorylated tyrosine residue within the regulatory site of MAP kinase (e.g.,Tyr185 in ERK-2). Cross-reactivity has been observed with the monophosphorylated tyrosine peptide of JNK.

면역원

synthetic peptide HTGFLTEpYVAT, corresponding to the phosphorylated form of ERK-activation loop.

애플리케이션

Monoclonal Anti-MAP Kinase, Monophosphorylated Tyrosine antibody has been used in:
  • immunoblotting
  • enzyme linked immunosorbent assay (ELISA)
  • dot-blot
  • immunocytochemistry
  • western blotting
  • immunofluorescence

생화학적/생리학적 작용

MAPK kinase (MAPKK) is the immediate upstream activator of the MAPK, MAPKK kinase (MAP3K), and MAP3K kinase (MAP4K) for the enzymes further upstream, respectively. The kinases in the MAPK level are activated by phosphorylation of both tyrosine (Y) and threonine (T) residues organized in a TXY motif. The residue in between the two phosphorylated residues determines the specificity of activation of the MAPKs. Phosphorylation of both tyrosine and threonine is essential for the full activation of all MAPKs.

물리적 형태

Solution in phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

제조 메모

Prepared from a culture supernatant of bioreactor grown hybridoma.

면책조항

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Mammalian MAP kinase signalling cascades
Chang L and Karin M
Nature, 410(6824), 37-37 (2001)
Sudhakaran Prabakaran et al.
Biophysical journal, 106(12), 2720-2728 (2014-06-19)
Mathematical models are extensively employed to understand physicochemical processes in biological systems. In the absence of detailed mechanistic knowledge, models are often based on network inference methods, which in turn rely upon perturbations to nodes by biochemical means. We have
Paradoxical results in perturbation-based signaling network reconstruction
Prabakaran S, et al.
Biophysical Journal, 106(12), 2720-2728 (2014)
Monophosphothreonyl extracellular signal-regulated kinases 1 and 2 (ERK1/2) are formed endogenously in intact cardiac myocytes and are enzymically active.
Sugden PH, et al.
Cellular Signalling, 23(2), 468-477 (2011)
H Cha et al.
The Journal of cell biology, 153(7), 1355-1367 (2001-06-27)
Phosphorylation of the extracellular signal-regulated kinases (ERKs) on tyrosine and threonine residues within the TEY tripeptide motif induces ERK activation and targeting of substrates. Although it is recognized that phosphorylation of both residues is required for ERK activation, it is

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