

Product description
This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. De
Source
Rabbit
Applications
WB
Reactivity
Human, Mouse,Rat
Dilution
WB 1:500-2000
Storage
-20°C/1 year
Specificity
This antibody detects endogenous levels of LYAG at Human/Mouse/Rat
Source/Purification
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Immunogen
Synthesized peptide derived from human LYAG
Uniprot No
P10253
Alternative names
Lysosomal alpha-glucosidase (EC 3.2.1.20) (Acid maltase) (Aglucosidase alfa) [Cleaved into: 76 kDa lysosomal alpha-glucosidase; 70 kDa lysosomal alpha-glucosidase]
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.221% sodium azide.
Clonality
Polyclonal
Background
This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. De
Other
Gene_name: GAA ; Protein_name: LYAG; Expression: Duodenum,Liver,Placenta,Plasma,Testis,Urine,
Mol.Wt (Da)
105 kD
Concentration
1 mg/ml
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