GeneBio Systems
Human HEXA ELISA Kit PicoKine®
Human HEXA ELISA Kit PicoKine®
SKU:EK2215
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Size: 96 wells/kit, with removable strips.
Storage: Store at 4℃ for 6 months, at -20℃ for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)
Form:
Reactivity: Human
Applications: ELISA
Application Details:
Gene Name: HEXA
Specificity: Natural and recombinant human HEXA
Background: Hexosaminidase A (alpha polypeptide), also known as HEXA, is an enzyme that in humans is encoded by the HEXA gene, located on the 15th chromosome. 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.
Immunogen: Expression system for standard: NS0; Immunogen sequence: M1-T529
Clonality:
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Purification:
Reconstitution:
Reference:
Uniprot ID: P06865
Host:
Concentration:
Conjugate:
Cross Reactivity: There is no detectable cross-reactivity with other relevant proteins.
Isotype:
Phospho_site:
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Observed Molecular Weight:
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Gene ID: 3073
Protein Name: Beta-hexosaminidase subunit alpha
Gene Full Name: hexosaminidase subunit alpha
Synonyms: HEXA; Hexosaminidase subunit A; TSD
