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Browse our GAA (GAA) ELISA Kits

Full name:
Glucosidase, Alpha, Acid ELISA Kits (GAA)
On www.antibodies-online.com are 20 Glucosidase, Alpha, Acid (GAA) ELISA Kits from 6 different suppliers available. Additionally we are shipping GAA Antibodies (72) and GAA Proteins (16) and many more products for this protein. A total of 114 GAA products are currently listed.
Synonyms:
E430018M07Rik, LYAG

GAA (GAA) ELISA Kits by Reactivity

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Mouse (Murine) Glucosidase, Alpha, Acid (GAA) interaction partners

  1. GAA deficiency results in reduced mTORC1 activation that is partly responsible for the skeletal muscle wasting phenotype and can be amerliorated by leucine supplementation.

  2. Results describe the inhibitory effects of Chana series chalcone derivatives on the activities of alpha-glucosidase (show AGLU ELISA Kits) and DPP-4 (show DPP4 ELISA Kits), and on adipocyte differentiation.

  3. Power and torque did not change with age in control animals, but declined significantly in acid 1-4 alpha-glucosidase (show AGLU ELISA Kits) knockout mice in three age groups.

  4. These studies suggest that hyase enhances penetration of enzyme into the tissues including muscle during ERT (show ELF3 ELISA Kits) and therefore hyase pretreatment may be important in treating Pompe disease.

Human Glucosidase, Alpha, Acid (GAA) interaction partners

  1. This is the first report of the alpha-glucosidase (show AGLU ELISA Kits) inhibitory activity of compounds 20, 26, and 29, and the findings support the important role of Eremanthus species as novel sources of new drugs and/or herbal remedies for treatment of type 2 diabetes.

  2. Compared with controls, GAA gene expression levels in coronary artery disease (CAD (show CAD ELISA Kits)) patients were significantly increased, suggesting that GAA may be involved in the CAD (show CAD ELISA Kits) development.

  3. Study reports on the clinical, biochemical, morphological, muscle imaging, and genetic findings of six adult Pompe patients from five unrelated families with the c.-32-13T>G GAA gene mutation in homozygous state. All patients had decreased GAA activity and elevated creatine kinase levels.

  4. glycogen (show GYS1 ELISA Kits) storage disease type II is caused by deficiency of GAA activity resulting from mutation of GAA gene

  5. RT-PCR followed by DNA sequence analysis of patients with Pompe disease revealed new variant in GAA gene resulting in aberrant splicing event.

  6. Findings indicate that GAA c.2238G > C (p.W746C) novel mutation is the most common mutation in mainland Chinese late-onset Pompe patients, as observed in Taiwanese patients expanding the genetic spectrum of the disease.

  7. this study shows several alterations distributed along the GAA gene in a sample of Brazilian families.

  8. GAA deficiency results in reduced mTORC1 activation that is partly responsible for the skeletal muscle wasting phenotype and can be amerliorated by leucine supplementation.

  9. The phenotype LO-GSDII with GAA mutation in the North of Italy seems not significantly different from other LO-GSDII populations in Europe or the USA.

  10. Data shows the largest informative family with late-onset Pompe disease described in the literature showing a peculiar complex set of mutations of GAA gene that may partially elucidate the clinical heterogeneity of this family.

GAA Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with GAA

  • glucosidase, alpha, acid (Gaa) Elisa Kit
  • glucosidase, alpha; acid (GAA) Elisa Kit
  • E430018M07Rik Elisa Kit
  • LYAG Elisa Kit

Protein level used designations for GAA

acid (Pompe disease, glycogen storage disease type II) , acid alpha-glucosidase , acid maltase , glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) , lysosomal alpha-glucosidase , aglucosidase alfa

GENE ID SPECIES
367562 Rattus norvegicus
14387 Mus musculus
2548 Homo sapiens
483352 Canis lupus familiaris
280798 Bos taurus
100173365 Pongo abelii
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