HEXA antibody [3F10]

Cannot supply to this region.

SKU:: GTX60574
Additional Names:: hexosaminidase subunit alpha , TSD
Application:: ELISA, Flow Cytometry, WB
Concentration:: 1 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Protein G Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Mouse
Reactivities:: Human
Buffer:: PBS, 0.05% Sodium azide.
Immunogen:: Purified recombinant fragment of human HEXA expressed in E. Coli.
Clone:: 3F10
Uniprot:: P06865
Synonyms:: beta-hexosaminidase subunit alpha;beta-N-acetylhexosaminidase subunit alpha;hexosaminidase A (alpha polypeptide);hexosaminidase subunit A;N-acetyl-beta-glucosaminidase subunit alpha;TSD
Extra Details:: This gene encodes the alpha subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Alpha subunit gene mutations lead to Tay-Sachs disease (GM2-gangliosidosis type I). [provided by RefSeq, Jul 2009]

Shipping Conditions:: Blue Ice