| 產(chǎn)品編號(hào) | 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. |
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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.
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| 研究領(lǐng)域 | 心血管 細(xì)胞生物 神經(jīng)生物學(xué) 細(xì)胞周期蛋白 細(xì)胞分化 |
| 抗體來(lái)源 | Rabbit |
| 克隆類型 | Polyclonal |
| 交叉反應(yīng) | Human (predicted: Mouse,Rat,Cow) |
| 產(chǎn)品應(yīng)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(cè)分子量 | |
| 細(xì)胞定位 | 細(xì)胞核 細(xì)胞漿 細(xì)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(xiàng) | 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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