AGA Antibodies

AND AGA ELISA kits, AGA Proteins

Many biological assays use antibodies to detect AGA, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with AGA in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop AGA antibodies...

We validate the specificity of these antibodies to AGA by testing them on tissues known to express AGA positively and negatively. Browse below to find the AGA antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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AGA Infographic by Boster Bio

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Human AGA Recombinant Protein

SDS-PAGE

$350
Cat # PROTP20933
Starting from 10ug

AGA Overview

Facts about N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase.

AGA 3D structure. Source: alphafold

N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase (AGA)

Cleaves the GlcNAc-Asn bond that joins oligosaccharides to the peptide of asparagine-linked glycoproteins. .

Gene Information

Human
Gene Name:	AGA
Uniprot:	P20933
Entrez:	175

Family

Belongs to:

Ntn-hydrolase family

Alternative Names

AGU; aspartylglucosaminidase; aspartylglucosylamine deaspartylase; ASRG; EC 3.5.1; EC 3.5.1.26; GA; glycosylasparaginase; N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase; N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase

Molecular Weight

Mass (kDA):
37.208 kDA

Genomic Context


Human

Location:	4q34.3
Sequence:	4; NC_000004.12 (177430774..177442503, complement)

Subcellular Localizations

Lysosome.

Diseases

Small For Gestational Age (disorder)
Fetal Growth Retardation
Celiac Disease
Growth Retardation
Diabetes Mellitus
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Hypertensive Disease
Malignant Neoplasms
Hemorrhage
Neoplasms
Insulin Resistance
Obesity
Androgenetic Alopecia

Atrophy
Malnutrition
Carcinoma
Pain
Pre-eclampsia
Infant, Very Low Birth Weight
Infective Disorder

Pathways

Pathogenesis
Translation
Secretion
Excretion
Transport
Coagulation
Localization
Insulin Secretion
Immune Response
Menarche
Cell Growth
Anagen
Brain Development

Inflammatory Response
Telogen
Aging
Drug Resistance
Platelet Aggregation
Bone Resorption
Hypersensitivity

PTMs

Phosphorylation
Cleavage
Glycosylation
Oxidation
Deamidation
Methylation
Deamination
Acylation

Amination
Deglycosylation
Carboxylation
Decarboxylation
Depoxidation
Biotinylation
Nitration
Reduction

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/AGA

References

PMID: 2401370 by Fisher K.J., et al. Cloning and sequence analysis of a cDNA for human glycosylasparaginase. A single gene encodes the subunits of this lysosomal amidase.

PMID: 1703489 by Ikonen E., et al. Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease.