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BZW2 Rabbit pAb (bs-8726R)  
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產(chǎn)品編號 bs-8726R
英文名稱 BZW2 Rabbit pAb
中文名稱 BZW2蛋白抗體
別    名 HSPC028; MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2; Basic leucine zipper and W2 domains 2; BZW 2; MST017; BZW2_HUMAN.  
Specific References  (2)     |     bs-8726R has been referenced in 2 publications.
[IF=3.923] Jin X et al. Role of the novel gene BZW2 in the development of hepatocellular carcinoma.J Cell Physiol. 2019 Feb 25.  IHC-P ;  Human.  
[IF=0.205] Wang S et al. Prognostic significance of BZW2 expression in lung adenocarcinoma patients. Int J Clin Exp Pathol. 2019 Dec 1;12(12):4289-4296. eCollection 2019.  IHC ;  Human.  
研究領域 心血管  細胞生物  神經(jīng)生物學  細胞周期蛋白  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human (predicted: Mouse,Rat,Cow)
產(chǎn)品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 48 kDa
檢測分子量
細胞定位 細胞核 細胞漿 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human BZW2: 151-250/419 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.

Function:
BZW2 belongs to the BZW family and contains one W2 domain. It may be involved in neuronal differentiation.

Similarity:
Belongs to the BZW family.
Contains 1 W2 domain.

SWISS:
Q9Y6E2

Gene ID:
28969

Database links:
UniProtKB/Swiss-Prot: Q9Y6E2.1

產(chǎn)品圖片
Sample:Raji (Human)Cell Lysate at 40 ug Primary: Anti-BZW2(bs-8726R)at 1/300 dilution Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution Predicted band size: 48kD Observed band size: 46kD
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