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> NADPH氧化酶活化蛋白p47抗體

產(chǎn)品資料

NADPH氧化酶活化蛋白p47抗體

NADPH氧化酶活化蛋白p47抗體
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  • 產(chǎn)品名稱:NADPH氧化酶活化蛋白p47抗體
  • 產(chǎn)品型號: p47-phox
  • 產(chǎn)品展商:單克隆抗體/多克隆抗體
  • 產(chǎn)品文檔:無相關(guān)文檔
簡單介紹
NADPH氧化酶活化蛋白p47抗體應(yīng)用于IHC、WB、 IF、IP、ELISA等科研實驗,按理化性質(zhì)和生物學(xué)功能IgM、IgG、IgA、IgE、IgD五類。按抗體的來源,可將其分為天然抗體和**抗體。NADPH氧化酶活化蛋白p47抗體生產(chǎn)每個流程都執(zhí)行嚴格的檢測標準,保證蛋白抗原產(chǎn)品質(zhì)量,質(zhì)量穩(wěn)定,實驗效果明顯。
產(chǎn)品描述

NADPH氧化酶活化蛋白p47抗體

規(guī)格:1mg/1ml


英文名: p47-phox

別名: Cyclin-dependent kinase inhibitor p27; cyclin-dependent kinase inhibitor 1B; cyclin-dependent kinase inhibitor 1B (p27, Kip1).

分子量: 43kDa

儲存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆類型:Polyclonal

亞型:IgG

純化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human p47-phox

交叉反應(yīng):Human, Mouse, Rat, Dog, Pig, Cow, Rabbit,

細胞定位:細胞漿

NADPH氧化酶活化蛋白p47抗體產(chǎn)品介紹:background: The heredity chronic granulomatous disease (CGF) has been linked to mutations in p47-phox and p67-phox. The cytosolic proteins p47-phox and p67-phox, also designated neutrophil cytosol factor (NCF)1 and NCF2, respectively, are required for activation of the superoxide-producing NADPH oxidase in neutrophils and other phagocytic cells. During activation of the NADPH oxidase, p47-phox and p67-phox migrate to the plasma membrane where they associate with cytochrome b558 and the small G protein Rac to form the functional enzyme complex. Both p47-phox and p67-phox contain two Src homology 3 (SH3) domains. The C-terminal SH3 domain of p67-phox has been shown to interact with the proline-rich domain of p47-phox, suggesting that p47-phox may faciliate the transport NADPH氧化酶活化蛋白p47抗體of p67-phox to the membrane. Function: NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production). Subunit: Interacts with NOXA1. Interacts with ADAM15. Interacts with TRAF4. Interacts with FASLG. Subcellular Location: Cytoplasm. Post-translational modifications: Phosphorylated by PRKCD; phosphorylation induces activation of NCF1 and NADPH oxidase activity. DISEASE: Defects in NCF1 are the cause of chronic granulomatous disease autosomal recessive cytochrome-b-positive type 1 (CGD1) [MIM:233700]. Chronic granulomatous disease is a genetically heterogeneous disorder characterized byNADPH氧化酶活化蛋白p47抗體 the inability of neutrophils and phagocytes to kill microbes that they have ingested. Patients suffer from life-threatening bacterial/fungal infections. Similarity: Contains 1 PX (phox homology) domain. Contains 2 SH3 domains. Gene ID: 653361 Database links: Entrez Gene: 653361 Human Entrez Gene: 17969 Mouse Entrez Gene: 114553 Rat Omim: 608512 Human SwissProt: P14598 Human SwissProt: Q09014 Mouse Unigene: 647047 Human Unigene: 655201 Human Unigene: 425296 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

NADPH氧化酶活化蛋白p47抗體產(chǎn)品應(yīng)用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (石蠟切片需做抗原修復(fù)) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究領(lǐng)域:細胞生物  **學(xué)  

儲存條件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

來源: Rabbit

外觀: Lyophilized or Liquid





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