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Aspartylglucosaminidase (AGA) ELISA Kits

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

list all ELISA KIts Gen GeneID UniProt
Anti-Human AGA AGA 175 P20933
Anti-Maus AGA AGA 11593 Q64191
Anti-Ratte AGA AGA 290923 P30919
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Weitere ELISA Kits für Aspartylglucosaminidase Interaktionspartner

Human Aspartylglucosaminidase (AGA) Interaktionspartner

  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 (zeige 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.

Mouse (Murine) Aspartylglucosaminidase (AGA) Interaktionspartner

Aspartylglucosaminidase (AGA) Antigen-Profil

Beschreibung des Gens

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.

Genbezeichner und Symbole assoziert mit AGA

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

Bezeichner auf Proteinebene für 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 , aspartylglucosaminidase , N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase-like

GENE ID SPEZIES
175 Homo sapiens
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
100592376 Nomascus leucogenys
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