产品名称 | Galactosidase alpha Antibody |
产品货号 | ABF302329 |
基因名称 | Galactosidase alpha |
蛋白名称 | Galactosidase alpha |
其他名称 | Alpha gal A; GALA; Galactosidase, alpha; GLA; Melibiase; |
SwissPro | Human:P06280     |
宿主种属 | Rabbit |
应用范围 | WB IHC ICC/IF IP FC |
稀释比例 | WB 1:500~1:2000 IHC 1:50~1:200 ICC/IF 1:50~1:200 IP 1:50 FC 1:80 |
反应种属 | Human |
克隆性 | Monoclonal |
免疫原 | A synthesized peptide derived from human Galactosidase alpha |
特异性 | Galactosidase alpha Antibody detects endogenous levels of total Galactosidase alpha |
同种型 | Rabbit IgG |
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°C/1 year |
背景资料 | 46kDa |
产品概述 | Defects in GLA are the cause of Fabry disease (FD) [MIM:301500]. FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. The disease consists of an inborn error of glycosphingolipid catabolism. |
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