AGA (Aspartylglucosaminidase, AGA)
Short Description: 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. [provided by RefSeq, Jan 2010].
More information related to gene AGA.
More information related to gene AGA.
Products related to AGA Gene:
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OriGene sr300123
RNAi
AGA
Species: Human
HPLC purified
- Application:
- RNA Interference
- Gene:
- Aspartylglucosaminidase
- Species:
- Human
- Purification:
- HPLC purified
Catalog No. ABIN3339919
$512.82
Plus shipping costs $50.00
1 kit
Shipping to:
United States
Delivery in 16 to 17 Business Days
ORF
Clon
Gateway Cloning Vector
pDONR223
Spectinomycin
unconjugated
Catalog No. ABIN5319264
$215.19
Plus shipping costs $50.00
2 μg
Shipping to:
United States
Delivery in 15 to 19 Business Days
Synonyms and alternative names related to AGA
- aspartylglucosaminidase (AGA)
- aspartylglucosaminidase (Aga)
- AGU
- ASRG
- AW060726
- GA
Gene-IDs for different species
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
Proteomics products related to AGA Gene
Other products related to AGA such as antibodies, ELISA kits and high-purity proteins are available on our partner website antibodies-online.com
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