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Merck
모든 사진(4)

문서

PLA0161

Sigma-Aldrich

Rabbit anti-MOF/MYST1 Antibody, Affinity Purified

Powered by Bethyl Laboratories, Inc.

동의어(들):

FLJ14040, K(lysine) acetyltransferase 8, Lysine acetyltransferase 8, MOF, MOZ, MYST histone acetyltransferase 1, MYST-1, MYST1, SAS2 and TIP60 protein 1, YBF2/SAS3, ZC2HC8, hMOF, histone acetyltransferase MYST1, ortholog of Drosophila males absent on the first (MOF), probable histone acetyltransferase MYST1

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About This Item

UNSPSC 코드:
12352203
NACRES:
NA.41

생물학적 소스

rabbit

Quality Level

항체 형태

affinity purified immunoglobulin

항체 생산 유형

primary antibodies

Grade

Powered by Bethyl Laboratories, Inc.

종 반응성

human, mouse

기술

immunohistochemistry: 1:500- 1:2,000
immunoprecipitation (IP): 2-5 μg/mg
western blot: 1:1,000- 1:10,000

수납 번호(accession number)

BAB13924.1

배송 상태

wet ice

저장 온도

2-8°C

타겟 번역 후 변형

unmodified

유전자 정보

면역원

The epitope recognized by PLA0161 maps to a region between residue 1 and 50 of human males absent on the first (MYST histone acetyltransferase 1) using the numbering given in entry BAB13924.1 (GeneID 84148).

물리적 형태

Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09% Sodium Azide

기타 정보

MOF is a member of the MYST family of histone acetyltransferases (HAT). MOF has been shown to be required for histone H4 lysine K16-specific acetylation. MOF interacts with ATM (ataxia-telangiectasia-mutated) and may participate in the activation of ATM in response to DNA damage.

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

12 - Non Combustible Liquids

WGK

nwg

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Mzwanele Ngubo et al.
Aging cell, 23(7), e14150-e14150 (2024-04-05)
Hutchinson-Gilford Progeria syndrome (HGPS) is a lethal premature aging disorder caused by a de novo heterozygous mutation that leads to the accumulation of a splicing isoform of Lamin A termed progerin. Progerin expression deregulates the organization of the nuclear lamina

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