产品名称 | GBA Antibody |
产品货号 | ABB6742 |
其他名称 | Alglucerase; betaGC; GBA1; GCase; GCB; GLUC; Glucosylceramidase; Imiglucerase; |
Gene ID | Human:P04062     |
SwissPro | Human:http://www.uniprot.org/uniprot/P04062     |
宿主种属 | Rabbit IgG |
应用范围 | WB IHC |
稀释比例 | WB 1:500~1:2000 IHC 1:50~1:200 |
反应种属 | Human Rat |
克隆性 | Monoclonal |
免疫原 | A synthesized peptide derived from human GBA |
保存液 | Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at +4°C short term. Store at -20°C long term. Avoid freeze / thaw cycle. |
纯化方式 | Affinity-chromatography |
保存条件 | -20 |
背景资料 | 60kDa |
产品概述 | Defects in GBA are the cause of Gaucher disease (GD) [MIM:230800]; also known as glucocerebrosidase deficiency. GD is the most prevalent lysosomal storage disease, characterized by accumulation of glucosylceramide in the reticulo-endothelial system. |
¥2200元
产品规格