Galactosidase, alpha (GLA) ELISA Kits

GLA encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. Additionally we are shipping GLA Antibodies (127) and GLA Proteins (18) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
GLA 2717 P06280
Anti-Rat GLA GLA 363494  
GLA 11605  
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Top GLA ELISA Kits at antibodies-online.com

Showing 10 out of 34 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.062 ng/mL 0.156-10 ng/mL 96 Tests Log in to see 15 to 17 Days
$832.83
Details
Mouse 7.81   96 Tests Log in to see 15 to 18 Days
$910.56
Details
Human 0.04 ng/mL 0.156-10 ng/mL   96 Tests Log in to see 2 to 3 Days
$713.90
Details
Guinea Pig
  96 Tests Log in to see 15 to 18 Days
$707.14
Details
Rabbit 1.875 pg/mL 3.125-200 pg/mL   96 Tests Log in to see 12 to 14 Days
$715.00
Details
Chicken 2.344 pg/mL 3.906-250 pg/mL   96 Tests Log in to see 12 to 14 Days
$715.00
Details
Pig 46.875 pg/mL 78.125-5000 pg/mL   96 Tests Log in to see 12 to 14 Days
$715.00
Details
Monkey 46.875 pg/mL 78.125-5000 pg/mL   96 Tests Log in to see 12 to 14 Days
$715.00
Details
Cow
  96 Tests Log in to see 15 to 18 Days
$707.14
Details
Sheep
  96 Tests Log in to see 15 to 18 Days
$707.14
Details

More ELISA Kits for GLA Interaction Partners

Human Galactosidase, alpha (GLA) interaction partners

  1. Mesenchymal stem cells with reduced GLA (show NAT8 ELISA Kits) activity are prone to apoptosis and senescence due to impaired autophagy and DNA repair capacity.

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

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

  4. Results found a novel heterozygous stop codon mutation in exon 1 of the GLA (show NAT8 ELISA Kits) 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.

  5. Study described the demographic data, wide clinical spectrum of phenotypes, and GLA (show NAT8 ELISA Kits) 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.

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

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

  8. High desphospho-uncarboxylated matrix Gla protein (show MGP ELISA Kits) 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

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

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

Mouse (Murine) Galactosidase, alpha (GLA) interaction partners

  1. Mice with alpha-galactosidase A deficiency show age-dependent and distinct deficits of the sensory system.

  2. In oocyte meiosis, GM130 (show GOLGA2 ELISA Kits) localization and expression patterns are regulated by FMNL1 (show FMNL1 ELISA Kits).

  3. The histological changes in Gla KO mice better resemble the type 2 later-onset phenotype observed in patients with residual alpha-galactosidase A activity.

  4. our findings imply that the alpha-GalA KO mouse is a good model in which to study the peripheral small fiber neuropathy exhibited by FD patients

  5. we demonstrate an age-dependent microvasculopathy of the mesenteric artery in a murine model of Fabry disease (galactosidase A-knockout mice) resulting from dysregulation of the vascular homeostatic enzyme endothelial nitric oxide synthase (eNOS (show NOS3 ELISA Kits))

  6. GM130 (show GOLGA2 ELISA Kits) regulates microtubule organization and might cooperate with the MAPK (show MAPK1 ELISA Kits) pathway to play roles in spindle organization, migration and asymmetric division during mouse oocyte maturation

  7. It suggested that there could be a combination of GLA deficiency and FVL (show F5 ELISA Kits) or other thrombosis-related gene defect in patients with genetic severe early-onset thrombosis.

  8. present Toll (show TLR4 ELISA Kits)-like receptor-dependent negative regulation of alpha-Gal-A as a mechanistic link between pathogen recognition and self lipid antigen induction for natural killer T cells

  9. Developed a novel recombinant lentiviral vector that engineers expression of alpha-galactosidase. Analysis of tissues at 26 wks demonstrated similar alpha-gal A enzyme activities but enhanced Gb3 reduction in hearts and kidneys compared with control.

  10. alpha-galactosidase A deficiency could be an important genetic modifier for the enhanced thrombosis associated with FV Leiden associated thrombosis.

GLA Antigen Profile

Antigen 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 Galactosidase, alpha (GLA) ELISA Kits

  • galactosidase, alpha (GLA) antibody
  • galactosidase, alpha (gla) antibody
  • alpha-galactosidase (agaN) antibody
  • aga (aga) antibody
  • alpha-galactosidase (agaL) antibody
  • alpha-galactosidase (SCO0541) antibody
  • alpha-galactosidase (rafA) antibody
  • alpha-galactosidase (melA) antibody
  • Alpha-galactosidase (galA) antibody
  • alpha-galactosidase A (ANI_1_2528074) antibody
  • alpha-galactosidase A (ANI_1_1502124) antibody
  • alpha-galactosidase A (AOR_1_390174) antibody
  • alpha-galactosidase A (CpipJ_CPIJ002066) antibody
  • alpha-galactosidase (aga) antibody
  • alpha-galactosidase A (MCYG_00962) antibody
  • alpha-galactosidase A (MCYG_00791) antibody
  • alpha-galactosidase (gla) antibody
  • alpha-galactosidase A (Tsp_02909) antibody
  • alpha-galactosidase A (Tsp_02508) antibody
  • galactosidase, alpha (Gla) antibody
  • golgi autoantigen, golgin subfamily a, 2 (Golga2) antibody
  • Ags antibody
  • alpha-GAL antibody
  • AO090005000217 antibody
  • AW555139 antibody
  • GALA antibody
  • GM130 antibody
  • MGC130872 antibody
  • mKIAA4150 antibody
  • SCF11.21 antibody
  • SMU.877 antibody
  • zgc:101584 antibody

Protein level used designations for Galactosidase, alpha (GLA) ELISA Kits

galactosidase, alpha , galactosidase alpha , Alpha-galactosidase A , alpha-D-galactosidase A , alpha-galactosidase A-like , alpha-galactosidase , Alpha-galactosidase , alpha-galactosidase A , agalsidase alfa , alpha-D-galactoside galactohydrolase 1 , alpha-gal A , melibiase , alpha-D-galactoside galactohydrolase , 130 kDa cis-Golgi matrix protein , Golgin subfamily A member 2 , SY11 protein , golgin-95

GENE ID SPECIES
280806 Bos taurus
465761 Pan troglodytes
703129 Macaca mulatta
734749 Xenopus laevis
100022779 Monodelphis domestica
100060370 Equus caballus
100145767 Xenopus (Silurana) tropicalis
100409841 Callithrix jacchus
100480888 Ailuropoda melanoleuca
100595113 Nomascus leucogenys
988766 Clostridium perfringens str. 13
1021683 Bifidobacterium longum NCC2705
1028243 Streptococcus mutans UA159
1095964 Streptomyces coelicolor A3(2)
1174420 Yersinia pestis CO92
1255824 Salmonella enterica subsp. enterica serovar Typhimurium str. LT2
2956399 Yersinia pseudotuberculosis IP 32953
3977399 Lactobacillus salivarius UCC118
4983447 Aspergillus niger CBS 513.88
4987403 Aspergillus niger CBS 513.88
5989256 Aspergillus oryzae RIB40
6032795 Culex quinquefasciatus
7264928 Bifidobacterium animalis subsp. lactis AD011
9223595 Arthroderma otae CBS 113480
9226616 Arthroderma otae CBS 113480
9450395 Brachyspira pilosicoli 95/1000
10899858 Trichinella spiralis
10903123 Trichinella spiralis
2717 Homo sapiens
363494 Rattus norvegicus
450083 Danio rerio
422188 Gallus gallus
532742 Bos taurus
11605 Mus musculus
100344610 Oryctolagus cuniculus
100718405 Cavia porcellus
407057 Sus scrofa
480988 Canis lupus familiaris
99412 Mus musculus
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