GLA/alpha-Galactosidase A, Human (HEK293, His)
GLA/alpha-Galactosidase A Protein, Human (HEK293, His), a recombinant human alpha-Galactosidase A produced in HEK293 cells, has a His tag at the C-terminus. alpha-Galactosidase A is the lysosomal exoglycosidase responsible for the hydrolysis of terminal α-galactosyl residues from glycoconjugates and is the defective enzyme causing Fabry disease[1].
Product Specifications
Product Name Alternative
GLA/alpha-Galactosidase A Protein, Human (HEK293, His), Human, HEK293
UNSPSC
12352202
Type
Recombinant Proteins
Assay Protocol
https://www.medchemexpress.com/cytokines/alpha-galactosidase-a-protein-human-hek293-his.html
Purity
98.0
Smiles
LDNGLARTPTMGWLHWERFMCNLDCQEEPDSCISEKLFMEMAELMVSEGWKDAGYEYLCIDDCWMAPQRDSEGRLQADPQRFPHGIRQLANYVHSKGLKLGIYADVGNKTCAGFPGSFGYYDIDAQTFADWGVDLLKFDGCYCDSLENLADGYKHMSLALNRTGRSIVYSCEWPLYMWPFQKPNYTEIRQYCNHWRNFADIDDSWKSIKSILDWTSFNQERIVDVAGPGGWNDPDMLVIGNFGLSWNQQVTQMALWAIMAAPLFMSNDLRHISPQAKALLQDKDVIAINQDPLGKQGYQLRQGDNFEVWERPLSGLAWAVAMINRQEIGGPRSYTIAVASLGKGVACNPACFITQLLPVKRKLGFYEWTSRLRSHINPTGTVLLQLENTMQMSLKDLLHHHHHH
Molecular Formula
2717 (Gene_ID) P06280 (L32-L429) (Accession)
Molecular Weight
50-60 kDa
References & Citations
[1]Fitzmaurice TF, et al. Human alpha-galactosidase A: high plasma activity expressed by the -30G-->A allele. J Inherit Metab Dis. 1997 Sep;20 (5) :643-57.|[2]Guce AI, et al. Catalytic mechanism of human alpha-galactosidase. J Biol Chem. 2010 Feb 5;285 (6) :3625-32.
Shipping Conditions
Dry ice
Storage Conditions
Stored at -80°C for 1 year
Scientific Category
Recombinant Proteins
Available Sizes
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