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產(chǎn)品名稱:Anti-GBA抗體*,β-葡萄糖腦苷脂酶抗體
中文名稱:β-葡萄糖腦苷脂酶抗體
英文名稱:Anti-GBA/Glucosidase beta
產(chǎn)品編號(hào):BYK-11779R
產(chǎn)品別名: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; Gba protein; GBA1; GC antibody GCase; GCB; GLCM_HUMAN; GLUC; Glucocerebrosidase (alt.); Glucocerebrosidase; GLUCOCEREBROSIDASE PSEUDOGENE; Glucosidase beta; Glucosidase, beta, acid; Glucosidase, beta; acid (includes glucosylceramidase); Glucosylceramidase; Imiglucerase; Lysosomal glucocerebrosidase.
本公司另供應(yīng)“β-葡萄糖腦苷脂酶抗體”的標(biāo)記有:Alexa Fluor 350 Alexa Fluor 488 Alexa Fluor 555 Alexa Fluor 647 AP APC Biotin Cy3 Cy5 Cy5.5 Cy7 FITC Gold HRP PE PE-Cy3 PE-CY5 PE-CY5.5 PE-CY7 RBITC.
產(chǎn)品規(guī)格:100ug/200ug
產(chǎn)品濃度: 1mg/1ml
抗體來源:兔源、鼠源、山羊
克 ?。?jiǎn)慰寺】贵w、多克隆抗體
抗體類型:一抗
性 狀: 凍干粉或液體
保存條件:Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Anti-GBA抗體*,β-葡萄糖腦苷脂酶抗體技術(shù)說明,產(chǎn)品*,由于篇幅原因,更多信息請(qǐng):
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Anti-ZNF217/FITC 熒光素標(biāo)記鋅指脂蛋白217抗體IgG
Anti-ZNF268(1a)/FITC 熒光素標(biāo)記鋅指脂蛋白-1a抗體IgG
Anti-ZNF268(1b)/FITC 熒光素標(biāo)記鋅指脂蛋白-1b抗體IgG
Anti-ZNF268(1c)/FITC 熒光素標(biāo)記鋅指脂蛋白-1c抗體IgG
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Anti-CD97/FITC 熒光素標(biāo)記CD97抗體IgG
Anti-CD99/E2 antigen/FITC 熒光素標(biāo)記CD99抗體IgG
Anti-XAF1/FITC 熒光素標(biāo)記XIAP相關(guān)因子1凋亡抑制蛋白抗體IgG
Anti-XBP-1/FITC 熒光素標(biāo)記細(xì)胞核轉(zhuǎn)錄因子X盒結(jié)合蛋白抗體IgG
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Anti-XIAP/FITC 熒光素標(biāo)記X-連鎖凋亡蛋白/性連鎖凋亡抑制蛋白抗體IgG
Anti-XRCC1/FITC 熒光素標(biāo)記X射線修復(fù)交叉互補(bǔ)蛋白/細(xì)胞堿基切除修復(fù)基因抗體IgG
Anti-YBX-1/FITC 熒光素標(biāo)記高保留轉(zhuǎn)錄因子抗體IgG
Anti-GBA抗體*,β-葡萄糖腦苷脂酶抗體產(chǎn)品介紹:
Beta-Glucosidase is a predominantly liver enzyme which efficiently hydrolyzes Beta-D-glucoside and Beta-D-galactoside. Defects in Beta-Glucosidase cause Gaucher disease, an inherited condition distinguished by the accumulation of glucosylceramide within the cells of the reticuloendothelial system. Beta-Glucosidase is used in enzyme replacement treatment aimed at treating Gaucher disease. The absorption of dietary flavonoid glycosides in humans involves a critical deglycosylation step that is mediated by epithelial Beta-glucosidases.
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