Aspartylglucosaminidase (AGA) ELISA Kits

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. Zusätzlich bieten wir Ihnen AGA Antikörper (24) und AGA Proteine (13) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
AGA 175 P20933
AGA 11593 Q64191
AGA 290923 P30919
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Top AGA ELISA Kits auf antikoerper-online.de

Showing 7 out of 7 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Affe 1.0 ng/mL 5-100 ng/mL   96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
Details
Huhn
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
Details
Schaf
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$707.14
Details
Human
0.312-20 ng/mL   96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$875.60
Details
Maus
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$875.60
Details
Ratte
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$875.60
Details
Schwein
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$1,029.60
Details

Weitere ELISA Kits für AGA Interaktionspartner

Human Aspartylglucosaminidase (AGA) Interaktionspartner

  1. We show that gene-silenced cells show specifically reduced AGA activity and store globotriaosylceramide. In gene-silenced cells, release of the neurotransmitter acetylcholine is significantly reduced, demonstrating that this model may be used to study specific neuronal functions such as neurotransmitter release in Fabry disease

  2. 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

  3. [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.

  4. Molecular mechanism for the autoproteolytic activation of aspartylglucosaminidase.

  5. 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.

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

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

  8. 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

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
  • AGU Antikörper
  • ASRG Antikörper
  • AW060726 Antikörper
  • GA 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

GENE ID SPEZIES
175 Homo sapiens
11593 Mus musculus
290923 Rattus norvegicus
100152203 Sus scrofa
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