Aspartylglucosaminidase Proteine (AGA)

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. Zusätzlich bieten wir Ihnen AGA Antikörper (32) und AGA Kits (18) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
AGA 175 P20933
AGA 11593 Q64191
AGA 290923 P30919
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Top AGA Proteine auf antikoerper-online.de

Showing 10 out of 17 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 30 bis 35 Tage
$5,465.26
Details
Insektenzellen Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 50 Days
$6,869.04
Details
Escherichia coli (E. coli) Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 30 bis 35 Tage
$5,465.26
Details
Insektenzellen Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 50 Days
$6,869.04
Details
Human Cells Human His tag 50 μg Anmelden zum Anzeigen 20 bis 21 Tage
$382.80
Details
Escherichia coli (E. coli) Human His tag 100 μg Anmelden zum Anzeigen 13 bis 16 Tage
$400.00
Details
Wheat germ Human GST tag 10 μg Anmelden zum Anzeigen 11 bis 12 Tage
$414.29
Details
Baculovirus infected Insect Cells Human His tag   50 μg Anmelden zum Anzeigen 13 bis 16 Tage
$400.00
Details
Escherichia coli (E. coli) Human Unkonjugiert SDS-PAGE analysis of Human AGA Protein. 100 μg Anmelden zum Anzeigen 11 bis 18 Tage
$568.54
Details
Escherichia coli (E. coli) Maus Unkonjugiert SDS-PAGE analysis of Mouse AGA Protein. 100 μg Anmelden zum Anzeigen 11 bis 18 Tage
$611.18
Details

AGA Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Human , , , ,
, ,
Mouse (Murine) ,
,
Rat (Rattus)

Weitere Proteine zu Aspartylglucosaminidase (AGA) Interaktionspartnern

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 Proteine). 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 Protein Überblick

Protein Überblick

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 Aspartylglucosaminidase Proteine (AGA)

  • aspartylglucosaminidase (AGA)
  • aspartylglucosaminidase (Aga)
  • AGU Protein
  • ASRG Protein
  • AW060726 Protein
  • GA Protein

Bezeichner auf Proteinebene für Aspartylglucosaminidase Proteine (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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