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重組人CD23蛋白

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產品編號bs-43216P
英文名稱Recombinant human FCER2/CD23 protein,N-His-Avi (HEK293)
中文名稱重組人CD23蛋白
別    名Fc EpsilonR II; FcεRII; Blast 2; Blast2; C type lectin domain family 4 member J; C-type lectin domain family 4, member J; CD 23; CD 23A; CD23 antigen; CD23A; CLEC 4J; CLEC4J; Fc epsilon RII; Fc fragment of IgE low affinity II receptor for; Fc fragment of IgE, low affinity II, receptor for (CD23); Fc of IgE, low affinity II, receptor for (CD23); Fc receptor IgE low affinity II alpha polypeptide; Fc receptor, IgE, low affinity II, alpha polypeptide, isoform CRA_a; FCE 2; FCE2; FCER 2; FCER2; FCER2A; IgE binding factor; IgE receptor lymphocyte; IgE-binding factor; IGEBF; Immunoglobulin E binding factor; Immunoglobulin E receptor, low affinity II; Low affinity immunoglobulin epsilon Fc receptor; Low affinity immunoglobulin epsilon Fc receptor membrane bound form; Low affinity immunoglobulin epsilon Fc receptor soluble form; Ly-42; Ly42; Lymphocyte antigen CD23; Lymphocyte IgE receptor; MGC93219  
理論分子量34.6kDa
性    狀Liquid
濃    度>1mg/ml
物    種Human
純    度>90% as determined by SDS-PAGE
純化方法AC
內毒素Not analyzed
表達系統HEK293 cell
標簽N-His-Avi
緩 沖 液PBS (pH=7.4)
保存條件Stored at -70℃ or -20℃. 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.
產品介紹The protein encoded by this gene is a B-cell specific antigen, and a low-affinity receptor for IgE. It has essential roles in B cell growth and differentiation, and the regulation of IgE production. This protein also exists as a soluble secreted form, then functioning as a potent mitogenic growth factor. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011]

SWISS:
P06734

Gene ID:
2208

CD23是一種II型跨膜糖蛋白,是存在于B細胞表面的IgE受體。在慢性B淋巴細胞白血病(CLL)和小B細胞淋巴瘤(SLL)為陽性,套細胞淋巴瘤和小核裂淋巴細胞淋巴瘤陰性。也表達于外周血B細胞的某些亞型、B淋巴細胞和EB病毒轉染的B淋巴瘤細胞系。CD23是慢性B淋巴細胞白血病,小B細胞淋巴瘤診斷和鑒別診斷有用的標記物。
產品圖片
The purity of the protein is greater than 90% as determined by reducing SDS-PAGE.
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