Aspartylglucosaminidase (AGA) Kits ELISA

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. De plus, nous expédions AGA Anticorps (24) et AGA Protéines (13) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
AGA 175 P20933
AGA 11593 Q64191
AGA 290923 P30919
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Top AGA Kits ELISA sur anticorps-enligne.fr

Showing 7 out of 7 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Singe 1.0 ng/mL 5-100 ng/mL   96 Tests Connectez-vous pour afficher 15 to 18 Days
$707.14
Détails
Poulet
  96 Tests Connectez-vous pour afficher 15 to 18 Days
$707.14
Détails
Mouton
  96 Tests Connectez-vous pour afficher 15 to 18 Days
$707.14
Détails
Humain
0.312-20 ng/mL   96 Tests Connectez-vous pour afficher 15 to 18 Days
$875.60
Détails
Rat
  96 Tests Connectez-vous pour afficher 15 to 18 Days
$875.60
Détails
Souris
  96 Tests Connectez-vous pour afficher 15 to 18 Days
$875.60
Détails
Porc
  96 Tests Connectez-vous pour afficher 15 to 18 Days
$1,029.60
Détails

Plus Kits ELISA pour AGA partenaires d'interaction

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 (Montrer GLS Kits ELISA). 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.

Mouse (Murine) Aspartylglucosaminidase (AGA) interaction partners

AGA profil antigène

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) anticorps
  • aspartylglucosaminidase (Aga) anticorps
  • AGU anticorps
  • ASRG anticorps
  • AW060726 anticorps
  • GA anticorps

Protein level used designations for AGA

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

GENE ID SPECIES
175 Homo sapiens
11593 Mus musculus
290923 Rattus norvegicus
100152203 Sus scrofa
Fournisseurs de qualité sélectionnés pour AGA (AGA) Kits ELISA
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