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| Antigenic Specificity | LYAG |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human |
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| Isotype | n/a |
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| Format | purified |
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| Size | 400 µl |
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| Concentration | n/a |
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| Applications | Immunohistochemistry (Paraffin): 1:1000, Western Blot: 1:1000-1:2000 |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | LYAG Polyclonal Antibody. This gene encodes 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. Three transcript variants encoding the same protein have been found for this gene. |
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| Immunogen | n/a |
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| Other Names | Lysosomal alpha-glucosidase; Acid maltase; Aglucosidase alfa; 76 kDa lysosomal alpha-glucosidase; 70 kDa lysosomal alpha-glucosidase; GAA |
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| Gene, Accession # | Entrez: 2548; Uniprot: P10253 |
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| Catalog # | PA5-71724 |
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| Price | |
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| Order / More Info | LYAG Antibody from INVITROGEN ANTIBODIES |
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| Product Specific References | n/a |
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