anti- Alpha galactosidase A antibody

Clonality	polyclonal
Host	Rabbit
Specificity	Human, Mouse, Rat
Tested Application	ELISA, IHC, IP, WB
Delivery Time	2 to 4 working days
Isotype	IgG
Form	liquid
Purification	Immunogen affinity purified
Purity	≥95% as determined by SDS-PAGE
Uniprot ID	P06280
Calculated MW	49 kDa
Ссылка на страницу на сайте производителя	ссылка
Инструкция	PDF
Storage	PBS with 0.02% sodium azide and 50% glycerol pH 7.3,-20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
Background	GLA, also named as Melibiase, Agalsidas and Alpha-galactosidase A, Belongs to the glycosyl hydrolase 27 family. It hydrolysis of 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.
Immunogen	galactosidase, alpha
Synonyms	Alpha galactosidase A, galactosidase, alpha
Recommended dilution	WB: 1:500-1:5000; IHC: 1:20-1:200; IP: 1:500-1:5000
Immunohistochemistry of paraffin-embedded human liver using FNab00328(GLA antibody) at dilution of 1:50
HeLa cells were subjected to SDS PAGE followed by western blot with FNab00328(GLA antibody) at dilution of 1:1000

Область использования: Поликлональные антитела	Производство:	Fine Biotech
	Метод:	Антитела
	Объем:	100µg
	Кат. номер:	FNab00328
Цена (с НДС 20%):	по запросу	В корзину
Наименование: anti- Alpha galactosidase A antibody. Примечание: