AGA Polyclonal Antibody

Supplier: Elabscience
Product Type: Antibody
Clonality: Polyclonal
Descritpion: 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. 
Research Areas:
Applications: WB,IHC,ELISA
Recommended Dilutions: WB 1:200-1:1000, IHC 1:15-1:50
Size: 200 uL
Concentration: 0.2mg/mL
Swissprot: P20933
Gene Accession: BC012392
Reactivity: Human,Mouse,Rat
Host: Rabbit
Isotype: IgG
Immunogen: Recombinant protein of human AGA
Formulation: PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Purification: Affinity purification
Conjugation: Unconjugated
Calculated MW: 37kDa
Tissue Specificity/Positive Control:
Cellular Localization: Endoplasmic reticulum,endoplasmic reticulum,Extracellular region or secreted,extracellular exosome,extracellular region,extracellular space,Lysosome,azurophil granule lumen,lysosome
Storage: Store at -20C. Avoid freeze / thaw cycles.

Product Link: https://www.elabscience.com/p-aga_polyclonal_antibody-33946.html
Manual Link: https://www.elabscience.com/viewpdf-33946-elabscience-E-AB-14518.PDF