ZNF799抗体

ZNF799抗体经ICC, IHC严格验证,品质保证.适用于多种种属反应性,被多篇文献引用并有用户反馈信息.确保特异性!产品具有以下特点:

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产品编号xy-16449R

英文名称ZNF799

中文名称锌指蛋白799抗体

别    名HIT 40; HIT40; HIT-40; MGC71805; OTTHUMP; Protein for MGC71805; Zinc finger protein 14; Zinc finger protein 799; Zinc finger protein 842; Zinc finger protein HIT 40; ZN799_HUMAN; ZNF799; ZNF842.  

说 明 书100ul  200ul

研究领域转录调节因子  锌指蛋白  表观遗传学  

抗体来源Rabbit

克隆类型Polyclonal

ZNF799抗体交叉反应 Human,

产品应用WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

分 子 量71kDa

细胞定位细胞核

性    状Lyophilized or Liquid

浓    度1mg/1ml

免 疫 原KLH conjugated synthetic peptide derived from human ZNF799

亚    型IgG

纯化方法affinity purified by Protein A

储 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件Store at -20 癈 for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20癈. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 癈.

PubMedPubMed

产品介绍background:

HIT-40 is a 643 amino acid nuclear protein that belongs to the Kr黳pel C2H2-type zinc-finger protein family. Containing eighteen C2H2-type zinc fingers and one KRAB domain, HIT-40 may be involved in transcriptional regulation. HIT-40 exists as two isoforms due to alternative splicing events, and is encoded by a gene that maps to human chromosome 19p13.2. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG families, and Fc?receptors. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19.

Function:

May be involved in transcriptional regulation.

Subcellular Location:

Nucleus.

Similarity:

Belongs to the krueppel C2H2-type zinc-finger protein family.

Contains 18 C2H2-type zinc fingers.

Contains 1 KRAB domain.

Gene ID:

90576