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GBA抗體,GBA抗原信息

發(fā)布時(shí)間:2022/5/26點(diǎn)擊次數(shù):161

產(chǎn)品名稱:Anti-GBA antibody

Rabbit  Anti-GBA  

別名:Glucosidase beta; Acid beta glucosidase; Acid beta-glucosidase; Alglucerase; Beta glucocerebrosidase; BETA GLUCOSIDASE, ACID; Beta-glucocerebrosidase; betaGC; D glucosyl N acylsphingosine glucohydrolase; D-glucosyl-N-acylsphingosine glucohydrolase; EC 3.2.1.45 ; Gba protein; GBA1; GC antibody GCase; GCB; GLCM_HUMAN; GLUC; Glucocerebrosidase (alt.); Glucocerebrosidase; GLUCOCEREBROSIDASE PSEUDOGENE; Glucosidase beta; Glucosidase, beta, acid; Glucosidase, beta; acid     

來(lái)源:Rabbit 

克隆類型:Polyclonal

濃度:1mg/ml

亞型:IgG

應(yīng)用: WB=1:500-1000 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500

反應(yīng): Human, Mouse,rat

免疫原:KLH conjugated synthetic peptide derived from human GBA

This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.


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GBA抗原

GBA antigen

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