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Rabbit Anti-BZW2  antibody (bs-8726R)
~~~促销,代码KX240301~~~
~~~促销,代码KX240302~~~
订购热线:400-901-9800
订购邮箱:sales@bioss.com.cn
订购QQ:  400-901-9800
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-8726R
英文名称 BZW2
中文名称 BZW2蛋白抗体
别    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.  
研究领域 心血管  细胞生物  神经生物学  细胞周期蛋白  细胞分化  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human (predicted: Mouse,Rat,Cow)
产品应用 WB=1:500-2000, IHC-P=1:100-500, IHC-F=1:100-500, IF=1:50-200, ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 48kDa
细胞定位 细胞核 细胞浆 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human BZW2: 151-250/419 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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

产品图片
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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