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H0163

Sigma-Aldrich

抗 组蛋白去乙酰化酶 4 (HDAC4) 抗体,小鼠单克隆

enhanced validation

clone HDAC4-144, purified from hybridoma cell culture

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

mouse

品質等級

共軛

unconjugated

抗體表格

purified from hybridoma cell culture

抗體產品種類

primary antibodies

無性繁殖

HDAC4-144, monoclonal

形狀

buffered aqueous solution

分子量

antigen ~140 kDa

物種活性

human, rat, mouse

加強驗證

independent
Learn more about Antibody Enhanced Validation

濃度

~2 mg/mL

技術

immunocytochemistry: suitable
immunoprecipitation (IP): suitable
western blot: 1-2 μg/mL using total cell extracts of NIH3T3 fibroblasts cells

同型

IgG2a

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... HDAC4(9759)
mouse ... Hdac4(208727)
rat ... Hdac4(363287)

相關類別

一般說明

单克隆抗组蛋白脱乙酰化酶4(HDAC4)(小鼠IgG2a同种型)来源于HDAC4-144 杂交瘤,该杂交瘤是由小鼠骨髓瘤细胞(NS1)和以对应于C末端添加赖氨酸并与KLH结合的人HDAC4氨基酸的合成肽免疫的BALB / c小鼠脾细胞融合而产生的。HDAC4属于II类哺乳动物HDAC。

應用

小鼠单克隆抗组蛋白脱乙酰化酶4(HDAC4)已被用于:
  • 酶联免疫吸附测定(ELISA)
  • 免疫印迹
  • 免疫细胞化学
  • 免疫沉淀

生化/生理作用

组蛋白脱乙酰化酶(HDAC)催化组蛋白的脱乙酰作用。HDAC4与转录抑制有关。它通过其入核转运和出核转运信号在细胞核和细胞质之间动态迁移。HDAC4与14-3-3和肌细胞增强因子2(Mef2)蛋白质的相互作用干扰了这种穿梭,因此分别将HDAC4导入细胞质和细胞核。

外觀

0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。

免責聲明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

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您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Erasers of Histone Acetylation: The Histone Deacetylase Enzymes
Seto E, et al.
Cold Spring Harbor Perspectives in Biology, 6 (2014)
Pan Luo et al.
Brain research bulletin, 156, 50-57 (2020-01-11)
Cerebral ischemia-reperfusion (I/R) can trigger neuronal death through several biologically plausible pathways, but its underlying neurobiological mechanisms remain unclear. In this study, we tested whether hyperpolarization-activated cyclic nucleotide-gated channel 1 (HCN1) is altered in I/R that contributes to neuron damage
Yali Kong et al.
Molecular cancer therapeutics, 10(9), 1591-1599 (2011-06-24)
Inhibitors of histone deacetylases (HDAC) are an important emerging class of drugs for the treatment of cancers. HDAC inhibitors are currently under evaluation in clinical trials as single agents and as sensitizers in combinations with chemotherapies and radiation therapy. Although
Histone deacetylase 4 possesses intrinsic nuclear import and export signals
Wang AH, et al.
Molecular and Cellular Biology, 21, 5992-6005 (2001)
Chi Ma et al.
The Journal of biological chemistry, 286(6), 4819-4828 (2010-12-02)
Histone deacetylase (HDAC) 7 is a member of the HDAC family of deacetylases. Although some of the HDAC proteins have been shown to regulate neuronal survival and death, whether HDAC7 has a similar role is not known. In this study

文章

Huntington's disease (HD) is an autosomal dominant, late-onset neurodegenerative disorder characterized by a selective neuronal cell death in the cortex and striatum leading to cognitive dysfunction, motor impairment and behavioral changes.

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