anti-Gla Gene Product (GLA) Antibodies

GLA encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins.

list all antibodies Gene Name GeneID UniProt
GLA 2717 P06280
GLA    
GLA    
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Top anti-GLA Antibodies at antibodies-online.com

Showing 10 out of 23 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Bat Rabbit Un-conjugated WB 50 μg Log in to see 7 to 9 Days
$551.83
Details
Human Rabbit Biotin ELISA, IHC (p)   100 μg Log in to see 7 to 9 Days
$463.83
Details
Human Rabbit Biotin ELISA, WB   100 μg Log in to see 7 to 9 Days
$537.17
Details
Human Rabbit FITC ELISA, WB   100 μg Log in to see 7 to 9 Days
$551.83
Details
Human Rabbit FITC ELISA, IHC (p)   100 μg Log in to see 7 to 9 Days
$581.17
Details
Mouse Rabbit Biotin ELISA, WB   100 μg Log in to see 7 to 9 Days
$581.17
Details
Mouse Rabbit FITC ELISA, WB   100 μg Log in to see 7 to 9 Days
$581.17
Details
Human Rabbit HRP ELISA, IHC (p)   100 μg Log in to see 7 to 9 Days
$581.17
Details
Mouse Rabbit HRP ELISA, WB   100 μg Log in to see 7 to 9 Days
$581.17
Details
Human Rabbit Biotin ELISA, WB   100 μg Log in to see 7 to 9 Days
$610.50
Details

GLA Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human ,
, ,
,
, ,
Mouse (Murine)


, ,
Rat (Rattus)


More Antibodies against GLA Interaction Partners

Human Gla Gene Product (GLA) interaction partners

  1. we review the various types of GLA (show NAT8 Antibodies) variants and recommend that pathogenicity be considered only when associated with elevated globotriaosylceramide in disease-relevant organs and tissues as analyzed by mass spectrometry.

  2. findings revealed the alternative splicing mechanism of GLA (show NAT8 Antibodies) (IVS4+919G>A), and a potential treatment for this specific genetic type of Fabry disease by amiloride in the future

  3. Results found a novel heterozygous stop codon mutation in exon 1 of the GLA (show NAT8 Antibodies) gene in female patients with Fabry Disease with methylation in the non-mutated allele thought to be associated with the clinical severity of the disease.

  4. Study described the demographic data, wide clinical spectrum of phenotypes, and GLA (show NAT8 Antibodies) mutation spectrum of Fabry disease in Korea. Most of the patients had classical Fabry disease, with a 4 times higher incidence than that of late-onset Fabry disease, indicating an underdiagnosis of mild, late-onset Fabry disease.

  5. we reviewed other small molecules that were reported to have a stabilizing effect on some GLA (show NAT8 Antibodies) missense mutations in vitro and might be developed to act in synergy or as an alternative to 1-deoxygalactonojirimycin

  6. No pathogenic mutations in the coding regions of the GLA (show NAT8 Antibodies) gene were identified in this group of patients and thus no Fabry disease was found in this study.

  7. High desphospho-uncarboxylated matrix Gla protein (show MGP Antibodies) level, reflecting a poor vitamin K status, seems to be associated with kidney damage and may be also a marker of cardiovascular risk in CKD patients

  8. Case Report: Kidney transplantation from a mother with unrecognized Fabry disease to her son with low alpha-galactosidase A activity.

  9. p.M187R GLA (show NAT8 Antibodies) mutation in Fabry disease causes a severe systemic and ophthalmologic phenotype, in both male and female patients.

  10. The results of the current study suggest that the GLA (show NAT8 Antibodies) haplotype D313Y does not lead to severe organ manifestations as seen in genotypes known to be causal for classical Fabry disease.

GLA Antigen Profile

Protein Summary

This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.

Gene names and symbols associated with anti-Gla Gene Product (GLA) Antibodies

  • galactosidase, alpha (GLA) antibody
  • GALA antibody

Protein level used designations for anti-Gla Gene Product (GLA) Antibodies

agalsidase alfa , alpha-D-galactosidase A , alpha-D-galactoside galactohydrolase 1 , alpha-gal A , alpha-galactosidase A , melibiase

GENE ID SPECIES
2717 Homo sapiens
Selected quality suppliers for anti-GLA (GLA) Antibodies
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