推荐产品
生物来源
rabbit
质量水平
偶联物
unconjugated
抗体形式
IgG fraction of antiserum
抗体产品类型
primary antibodies
克隆
polyclonal
表单
buffered aqueous solution
分子量
antigen ~134 kDa
种属反应性
human, mouse
技术
immunoprecipitation (IP): 5-10 μg using RIPA extract of 500 μg of 293T cells expressing recombinant mouse HDAC6.
microarray: suitable
western blot: 1:1,000 using 293T cells expressing recombinant mouse HDAC6 in a chemiluminescent detection system.
UniProt登记号
运输
dry ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
human ... HDAC6(10013)
mouse ... Hdac6(15185)
一般描述
Anti-Histone Deacetylase 6 (HDAC6), is produced in rabbit using a synthetic peptide corresponding to amino acid residues 1199-1213 of human HDAC6. Mammalian HDACs can be divided into three classes according to sequence homology. Class I consists of the yeast Rpd3-like proteins HDAC1, HDAC2, HDAC3 and HDAC8. Class II consists of the yeast Hda1-like proteins HDAC4, HDAC5, HDAC6, HDAC7, HDAC9 and HDAC10. Class III consists of the yeast Sir2-like proteins. Class I HDACs are ubiquitously expressed, most class II HDACs are tissue-specific. Class II HDACs are larger than those of class I and their catalytic domain is located in the carboxy-terminal half of the protein. HDAC6 is a unique deacetylase among class II members in that it contains a duplicate of the catalytic domain in its NH2 terminus as well. The deacetylase activity of class II HDACs is regulated by subcellular localization. Endogenous HDAC6 is predominantly cytoplasmic where it associates with microtubules and functions as an a-tubulin deacetylase. HDAC6 contains a conserved zinc finger motif that is probably involved in the regulation of ubiquitination. The gene HDAC6 is mapped to human chromosome Xp11.23.
特异性
Anti-Histone Deacetylase 6 (HDAC6) recognizes human and mouse HDAC6 (~134 kDa). Detection of HDAC6 by immunoblotting is specifically inhibited with the immunizing peptide. Additional nonspecific bands of approx. 50 kDa may be detected in various extract preparations.
免疫原
synthetic peptide corresponding to amino acid residues 1199-1213 of human HDAC6. The corresponding sequence in mouse differs by one amino acid.
应用
Anti-Histone Deacetylase 6 (HDAC6) recognizes human and mouse HDAC6 (~134 kDa). Applications include immunoblotting, immunoprecipitation, immunocytochemistry and immunohistochemistry.
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunohistochemistry (1 paper)
Western Blotting (1 paper)
Immunohistochemistry (1 paper)
Western Blotting (1 paper)
生化/生理作用
Histone Deacetylase 6 (HDAC6) is an enzyme responsible for deacetylation of histones. HDAC6 is a part of transcriptional corepressor complexes. Overexpression or destruction of HDAC6 may lead to Alzheimer, Parkinson and cardiovascular diseases. Overexpression of HDAC6 is implicated in various cancers like malignant melanoma, lung and bladder cancer. It promotes tumorigenesis, cell migration and invasion. HDAC6 also regulates the expression of critical immune system molecules, targets of chemotherapy like programmed death receptor-1 (PD-1). Mutations in HDAC6 causes X-linked chondrodysplasia.
外形
0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。
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.
未找到合适的产品?
试试我们的产品选型工具.
法规信息
常规特殊物品
历史批次信息供参考:
The human histone deacetylase family
Experimental Cell Research, 262(2), 75-83 (2001)
The class I-specific HDAC inhibitor MS-275 modulates the differentiation potential of mouse embryonic stem cells
Biology Open, 2(10), 1070-1077 (2013)
Histone deacetylase 6 in cancer
Journal of Hematology & Oncology, 11(1), 111-111 (2018)
Activation of autophagy in mesenchymal stem cells provides tumor stromal support
Carcinogenesis, 32(7), 964-972 (2011)
iScience, 27(1), 108689-108689 (2024-01-16)
High glucose has been proved to impair cognitive function in type 2 diabetes, but the underlying mechanisms remain elusive. Here, we found that high glucose increased transcription factors' SP1 O-GlcNAcylation in regulatory T (Treg) cells. Glycosylated SP1 further enhanced HDAC2
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门