HEXA antibody
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


HEXA antibody
Background :
This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons, the underlying cause of neurodegenerative disorders termed the GM2 gangliosidoses, including Tay-Sachs disease (GM2-gangliosidosis type I) . Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.Synonyms :
Beta-hexosaminidase subunit alpha|Beta-N-acetylhexosaminidase subunit alpha (Hexosaminidase subunit A) |N-acetyl-beta-glucosaminidase subunit alpha|HEXAGene ID :
3073UniProt :
P06865Host :
RabbitReactivity :
Human, Mouse, RatImmunogen :
Hexosaminidase A (alpha polypeptide)Target :
HEXAClonality :
PolyclonalIsotype :
IgGApplications :
ELISA, WB, IHCField of Research :
Neuroscience, MetabolismPurification :
Immunogen affinity purifiedDilution :
WB: 1:500 - 1:2000; IHC: 1:50 - 1:200Purity :
≥95% as determined by SDS-PAGEForm :
LiquidMolecular Weight :
60 kDaShipping Conditions :
4°C with ice bagStorage Conditions :
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20°C for 12 months (Avoid repeated freeze / thaw cycles.)Tested Applications :
ELISA, WB, IHC
