例句In this paper, the method was based on the hydrolysis of lactose by a β-galactosidase and the liberated glucose was determined.该法基于乳糖酶对乳糖的水解反应,测定所生成的葡萄糖量。 概述 概述 α-半乳糖苷酶(α-GAL,也称为α-GALA)是一种糖苷水解酶,可水解糖脂和糖蛋白中的末端α-半乳糖...
Fabry disease is caused by a deficiency of & alpha;-galactosidase A (GLA) leading to the lysosomal accumulation of globotriaosylceramide (Gb3) and other glycosphingolipids. Fabry patients experience significant damage to the heart, kidney, and blood vessels that can be fatal. Here we apply...
IP result of anti-Alpha Galactosidase A (IP:15428-1-AP, 3ug; Detection:15428-1-AP 1:1000) with HEK-293 cells lysate 1800ug.View All Images (16) IHC staining of human liver cancer using 15428-1-AP Immunohistochemical analysis of paraffin-embedded human liver cancer tissue slide using 15428...
66121-1-Ig targets Alpha Galactosidase A in WB, IHC, IF/ICC, ELISA applications and shows reactivity with human samples. Tested Applications WB, IHC, IF/ICC, ELISA Application Description Cited Applications WB Tested Reactivity human Cited Reactivity human Immunogen Alpha Galactosidase A fusion prot...
摘要: A review of the article "Alpha-galactosidase A activity levels in Turkish male hemodialysis patients," by S. Duman and colleagues, which appeared in the periodical "Therapeutic Apheresis and Dialysis" in 2012, is presented.年份: 2013 ...
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摘要: An isolated polypeptide having alpha-galactosidase activity and characterized as having a pH optimum in the range of 5.0-7.0, and a temperature optimum within the range of 50-70° C. The alpha-galactosidase is derived from Aspergillus niger....
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Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 gene Homozygous loss-of-function mutations in the gene coding for the homeobox transcription factor PDX1 leads to pancreatic agenesis, whereas certain heterozyg... X Wang,S Chen...
The present application provides for compositions comprising α-galactosidase A in combination with an active site-specific chaperone for the α-galactosidase A, and methods for treating Fabry disease in a subject in need thereof, that includes a method of administering to the subject such ...