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Antigenic Specificity | Glucosidase, Alpha, Acid (GAA) (N-Term) |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | human |
Isotype | n/a |
Format | affinity purified |
Size | 50 µg |
Concentration | n/a |
Applications | Western Blotting (WB) |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | GAA is acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. |
Immunogen | GAA antibody was raised using the N terminal of GAA corresponding to a region with amino acids FGVIVRRQLDGRVLLNTTVAPLFFADQFLQLSTSLPSQYITGLAEHLSPL |
Other Names | E430018M07Rik|LYAG |
Gene, Accession # | Gene ID: 2548 |
Catalog # | ABIN635720 |
Price | |
Order / More Info | Glucosidase, Alpha, Acid (GAA) (N-Term) Antibody from ANTIBODIES-ONLINE GmbH |
Product Specific References | n/a |
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