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Aspartylglucosaminidase (AGA) ELISA Kits

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Mouse AGA AGA 11593 Q64191
Anti-Rat AGA AGA 290923 P30919
Anti-Human AGA AGA 175 P20933
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More ELISA Kits for Aspartylglucosaminidase Interaction Partners

Mouse (Murine) Aspartylglucosaminidase (AGA) interaction partners

Human Aspartylglucosaminidase (AGA) interaction partners

  1. study reports 2 novel aspartylglucosaminidase gene mutations, one in Qatari twins with an early, perinatal presentation not previously described for aspartylglucosaminuria and the other in 3 Turkish children with newly diagnosed aspartylglucosaminuria and a more classical disease course

  2. [review] Natural killer (NK) cell tumors, subtypes of myeloid leukemias and T-cell lymphomas respond to ASNase; ovarian carcinomas and other solid tumors have been proposed as additional targets for ASNase, with a potential role for glutaminase (show GLS ELISA Kits). activity.

  3. Molecular mechanism for the autoproteolytic activation of aspartylglucosaminidase.

  4. A new point mutation, c.44T>G, found in a Finnish compound heterozygote causes a L15R AA substitution in the signal sequence of the AGA enzyme, affecting AGA translocation by altering a critical hydrophobic core structure in the signal sequence.

  5. aspartylglucosaminidase may have a role in development of congenital disorders of glycosylation type I

  6. The amino acid substitutions in aspartylglucosaminidase responsible for aspartylglucosaminuria were classified and divided in three groups.

  7. Increased AGA plasma activity, although a consistent finding in congenital disorders of glycosylation patients, is not specific to this group of disorders.

Aspartylglucosaminidase (AGA) Antigen Profile

Antigen Summary

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. Alternatively spliced transcript variants have been identified.

Gene names and symbols associated with AGA

  • aspartylglucosaminidase (Aga) antibody
  • aspartylglucosaminidase (AGA) antibody
  • aspartylglucosaminidase (aga) antibody
  • aspartylglucosaminidase (LOC751092) antibody
  • aspartylglucosaminidase (LOC100119424) antibody
  • aspartylglucosaminidase (LOC100231883) antibody
  • AGA antibody
  • AGU antibody
  • ASRG antibody
  • AW060726 antibody
  • GA antibody
  • MGC77327 antibody
  • NV17046 antibody
  • zgc:77327 antibody

Protein level used designations for AGA

N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase , N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase , glycosylasparaginase , N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase , aspartylglucosaminidase , N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase-like , aspartylglucosylamine deaspartylase

GENE ID SPECIES
11593 Mus musculus
290923 Rattus norvegicus
422558 Gallus gallus
461616 Pan troglodytes
475638 Canis lupus familiaris
496249 Xenopus laevis
511345 Bos taurus
566517 Danio rerio
699740 Macaca mulatta
751092 Bombyx mori
100119424 Nasonia vitripennis
100231883 Taeniopygia guttata
100453921 Pongo abelii
175 Homo sapiens
100592376 Nomascus leucogenys
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