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Rabbit Anti-ZNF799/AP Conjugated antibody (bs-16449R-AP)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-16449R-AP
英文名稱 Rabbit Anti-ZNF799/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標記的鋅指蛋白799抗體
別    名 HIT 40; HIT40; HIT-40; MGC71805; OTTHUMP00000209843; Protein for MGC71805; Zinc finger protein 14; Zinc finger protein 799; Zinc finger protein 842; Zinc finger protein HIT 40; ZN799_HUMAN; ZNF799; ZNF842.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 轉錄調節因子  鋅指蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, 
產品應用 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 71kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZNF799
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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.
產品介紹 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.

Database links:

Entrez Gene: 90576 Human

SwissProt: Q96GE5 Human

Unigene: 546637 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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