HEXB Break Apart FISH Probe

Hexosaminidase B is the beta 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. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
HEXBBA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
HEXBBA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

Hexosaminidase B is the beta 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. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]

Gene Details

Gene Symbol : HEXB

Gene Name : Hexosaminidase subunit beta

Chromosome : CHR 5: 746,400,22-747,212,87

Locus : 5q13.3

Alt. Genes : ZNF263

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