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Key Documents
G7163
α-Galactosidase, positionally specific from Escherichia coli
recombinant, expressed in E. coli, buffered aqueous solution
Synonim(y):
1,6-alpha-D-galactoside galactohydrolase, alpha-Galactosidase, melibiase
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About This Item
Numer CAS:
Numer MDL:
Kod UNSPSC:
12352204
NACRES:
NA.32
Polecane produkty
rekombinowane
expressed in E. coli
Poziom jakości
Postać
buffered aqueous solution
aktywność właściwa
≥20 units/mg protein
masa cząsteczkowa
80 kDa
Warunki transportu
wet ice
temp. przechowywania
2-8°C
informacje o genach
Escherichia coli CFT073 ... melA(1037886)
Powiązane kategorie
Działania biochem./fizjol.
Cleaves α(1→3)- and α(1→6)-linked, non-reducing terminal galactose from complex carbohydrates and glycoproteins. It is particularly efficient for removing α-linked galactose under conditions where the pH must be neutral or above, for example, with live cells.
Definicja jednostki
One unit will hydrolyze 1 μmole of p-nitrophenyl α-D-galactopyranoside per min at pH 6.5 at 25 °C.
Postać fizyczna
This product is a sterile-filtered aqueous buffered solution.
This page may contain text that has been machine translated.
inhibitor
Numer produktu
Opis
Cennik
substrat
Kod klasy składowania
12 - Non Combustible Liquids
Klasa zagrożenia wodnego (WGK)
WGK 2
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Certyfikaty analizy (CoA)
Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.
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Fabry disease (FD) is a genetic disorder resulting from deficiency of the lysosomal enzyme α-galactosidase A (α-Gal A), which leads to globotriaosylceramide (GL-3) accumulation in multiple tissues. We report on the safety and pharmacodynamics of migalastat hydrochloride, an investigational pharmacological
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Fabry disease (FD) is a rare, X-linked lysosomal storage disorder with multiorgan involvement. FD is caused by a partial or total deficit of α-galactosidase A enzyme, which is responsible for the accumulation of glycosphingolipids in a variety of cell types.
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