Rat Glucosidase Alpha, Acid (GaA) ELISA Kit | GaA elisa kit
Rat Glucosidase Alpha, Acid (GaA) ELISA Kit
No significant cross-reactivity or interference between Glucosidase Alpha, Acid (GaA) and analogues was observed.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
NCBI and Uniprot Product Information
NCBI Description
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. [provided by RefSeq, Jul 2008]
Uniprot Description
GAA: Essential for the degradation of glygogen to glucose in lysosomes. Defects in GAA are the cause of glycogen storage disease type 2 (GSD2); also called acid alpha-glucosidase (GAA) deficiency or acid maltase deficiency (AMD). GSD2 is a metabolic disorder with a broad clinical spectrum. The severe infantile form, or Pompe disease, presents at birth with massive accumulation of glycogen in muscle, heart and liver. Cardiomyopathy and muscular hypotonia are the cardinal features of this form whose life expectancy is less than two years. The juvenile and adult forms present as limb-girdle muscular dystrophy beginning in the lower limbs. Final outcome depends on respiratory muscle failure. Patients with the adult form can be free of clinical symptoms for most of their life but finally develop a slowly progressive myopathy. Belongs to the glycosyl hydrolase 31 family.
Protein type: Hydrolase; Contractile; EC 3.2.1.20; Carbohydrate Metabolism - starch and sucrose; Carbohydrate Metabolism - galactose
Chromosomal Location of Human Ortholog: 17q25.2-q25.3
Cellular Component: membrane; lysosomal membrane; lysosome
Molecular Function: alpha-glucosidase activity; maltase activity; carbohydrate binding
Biological Process: heart morphogenesis; maltose metabolic process; tissue development; glycogen catabolic process; vacuolar sequestering; glucose metabolic process; locomotory behavior; sucrose metabolic process; muscle maintenance; neuromuscular process controlling posture; lysosome organization and biogenesis; diaphragm contraction; neuromuscular process controlling balance; regulation of the force of heart contraction; cardiac muscle contraction
Disease: Glycogen Storage Disease Ii
Research Articles on GaA
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Product Notes
The Rat GaA gaa (Catalog #AAA2025215) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA2025215 ELISA Kit recognizes Rat GaA. It is sometimes possible for the material contained within the vial of "Glucosidase Alpha, Acid (GaA), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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