E-KAB-0257
Human GLA Alpha Antibody Pair Set
Größe
£793.80
War £882.00
- SKU:
- E-KAB-0257
- Zusätzliche Namen:
- GLA,Agalsidase,Alpha-galactosidase A,Alpha-D-galactosidase A,Alpha-D-galactoside galactohydrolase,Galactosylgalactosylglucosylceramidase GLA
- Anwendung:
- ELISA
- Spezies-Reaktivität:
- Human
- Lagerbedingungen:
- -20[o]C Avoid freeze/thaw cycles.
- Hersteller:
- Elabscience
- Reaktivitäten:
- Human
- Buffer:
- Capture Antibody:PBS with 0.04% Proclin 300, 50% glycerol, pH 7.4, Detection Antibody:PBS with 0.04% Proclin 300, 1% protective protein, 50% glycerol, pH 7.4
- Immunogen:
- GLα
- Formulierung:
- Capture Antibody:PBS with 0.04% Proclin 300, 50% glycerol, pH 7.4, Detection Antibody:PBS with 0.04% Proclin 300, 1% protective protein, 50% glycerol, pH 7.4
- Uniprot:
- P06280
- Synonyme:
- agalsidase alfa;alpha-D-galactosidase A;Alpha-D-galactoside galactohydrolase;alpha-D-galactoside galactohydrolase 1;alpha-gal A;alpha-galactosidase A;GALA;galactosylgalactosylglucosylceramidase GLA;melibiase
- Weitere Details:
- GLA,also named as Melibiase,Agalsidase and Alpha-galactosidase A,belongs to the glycosyl hydrolase 27 family. It hydrolyzes terminal,non-reducing alpha-D-galactose residues in alpha-D-galactosides,including galactose oligosaccharides,galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy (ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease,a lysosomal storage disease.
- Versandbedingungen:
- Blue Ice