PLA0161
Rabbit anti-MOF/MYST1 Antibody, Affinity Purified
Powered by Bethyl Laboratories, Inc.
别名:
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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所有图片(4)
About This Item
UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源
rabbit
质量水平
抗体形式
affinity purified immunoglobulin
抗体产品类型
primary antibodies
等级
Powered by Bethyl Laboratories, Inc.
种属反应性
human, mouse
技术
immunohistochemistry: 1:500- 1:2,000
immunoprecipitation (IP): 2-5 μg/mg
western blot: 1:1,000- 1:10,000
登记号
BAB13924.1
运输
wet ice
储存温度
2-8°C
靶向翻译后修饰
unmodified
基因信息
rabbit ... MOF/MYST1(84148)
免疫原
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).
外形
Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09% Sodium Azide
其他说明
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.
免责声明
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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储存分类代码
12 - Non Combustible Liquids
WGK
nwg
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
常规特殊物品
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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