Product Name	BZW2
Chinese Name	BZW2蛋白抗体
Alias	HSPC028; MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2; Basic leucine zipper and W2 domains 2; BZW 2; MST017; BZW2_HUMAN.
literatures	Specific References  (2)     |     SL8726R 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.   PubMed:30805927 [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.   PubMed:31933829
Research Area	Cardiovascular  Cell biology  Neurobiology  Cyclin  Cell differentiation
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	Human,  (predicted: Mouse, Rat, Cow, )
Applications	WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 （Paraffin sections need antigen repair） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight	48kDa
Cellular localization	The nucleus cytoplasmic The cell membrane
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human BZW2: 151-250/419
Lsotype	IgG
Purification	affinity purified by Protein A
Buffer Solution	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed	PubMed
Product Detail	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
Product Picture	Sample:Raji (Human)Cell Lysate at 40 ug Primary: Anti-BZW2(SL8726R)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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