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Glucosidase, Alpha, Acid (GAA) ELISA Kits

GAA encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Additionally we are shipping GAA Antibodies (53) and GAA Proteins (14) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
GAA 367562 Q6P7A9
GAA 14387 P70699
GAA 2548 P10253
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Top GAA ELISA Kits at antibodies-online.com

Showing 4 out of 16 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.057 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
$663.16
Details
Mouse 14.3 pg/mL 31.25-2000 pg/mL 96 Tests Log in to see 9 to 11 Days
$682.11
Details
Rat 0.31-20 ng/mL   96 Tests Log in to see 9 to 11 Days
$720.00
Details
Cow
0.78-50 ng/mL   96 Tests Log in to see 11 to 13 Days
$1,029.60
Details

More ELISA Kits for GAA Interaction Partners

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. 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.

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

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

  4. 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.

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

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

  7. 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.

  8. 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.

  9. 7 of 27 in: Gene. 2014 Mar (show IRF1 ELISA Kits) 1;537(1) Novel GAA sequence variant c.1211 A>G reduces enzyme activity but not protein expression in infantile and adult onset Pompe disease.

  10. This study demonstrates that the c.-32-13T>G mutation of GAA gene abrogates the binding of the splicing factor (show SLU7 ELISA Kits) U2AF65 (show U2AF59 ELISA Kits) to the polypyrimidine tract of exon 2 and that several splicing factors affect exon 2 inclusion.

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.

Gene names and symbols associated with GAA

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

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
Selected quality suppliers for GAA (GAA) ELISA Kits
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