NAGA (NM_000262) Human Recombinant Protein
Product Specifications
Background
NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of Schindler disease types I and II (type II also known as Kanzaki disease) . [provided by RefSeq, Jul 2008]
Synonyms
D22S674; GALB
Gene ID
4668
UniProt
P17050, A0A024R1Q5
Accession Number mRNA
NM_000262
Chromosomal Location
22q13.2
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Glycosphingolipid biosynthesis - globo series, Lysosome
Field of Research
Glycosphingolipid biosynthesis - globo series, Lysosome
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome
Molecular Weight
44.7 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
NAGA
Species
Human
Protein ID
NP_000253
Overview
Recombinant protein of human N-acetylgalactosaminidase, alpha- (NAGA)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/4668
Uniprot URL
https://www.uniprot.org/uniprot/P17050
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000262
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000253
Curated Selection
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