AGA Proteins
(Aspartylglucosaminidase (AGA))
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].
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9 results
AGA
Origin: Human
Host: Wheat germ
Recombinant
WB, ELISA, AA, AP
1 image
AGA
Origin: Human
Host: Escherichia coli (E. coli)
Recombinant
> 95 %
SDS, WB, Imm, PC
AGA
Origin: Mouse
Host: Escherichia coli (E. coli)
Recombinant
> 95 %
SDS, WB, Imm, PC
AGA
Origin: Human
Host: Escherichia coli (E. coli)
Recombinant
> 90 % pure
SDS
AGA
Origin: Human
Host: Baculovirus infected Insect Cells
Recombinant
> 90% by SDS-PAGE
SDS
AGA
Origin: Elizabethkingia miricola
Host: Yeast
Recombinant
> 90 %
ELISA
Aliases for AGA Proteins
aspartylglucosaminidase (AGA) Proteinsaspartylglucosaminidase (Aga) Proteins
AGU Proteins
ASRG Proteins
AW060726 Proteins
GA Proteins
Did you look for something else?
- AFT1 Proteins
- AFMID Proteins
- AFG3L2 Proteins
- AFF4 Proteins
- AFF2 Proteins
- AFAP1L2 Proteins
- AFAP Proteins
- Afamin Proteins
- AF9 Proteins
- AES Proteins
- AEN Proteins
- AEBP2 Proteins
- AEBP1 Proteins
- Advillin Proteins
- ADSSL1 Proteins
- ADSS Proteins
- ADRP Proteins
- ADRM1 Proteins
- Adrenomedullin Proteins
- ADRBK2 Proteins
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