HEXA rabbit pAb

HEXA rabbit pAb

AO-06-ES3963-100

HEXA rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3963
Product nameHEXA rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameHEXA; Beta-hexosaminidase subunit alpha; Beta-N-acetylhexosaminidase subunit alpha; Hexosaminidase subunit A; N-acetyl-beta-glucosaminidase subunit alpha
Size100μL
Unit price ($)248
Human gene ID3073
Human Swiss-ProtP06865
SourceRabbit
IsotypeIgG
TargetHEXA
Fields>>Other glycan degradation;>>Various types of N-glycan biosynthesis;>>Amino sugar and nucleotide sugar metabolism;>>Glycosaminoglycan degradation;>>Sphingolipid metabolism;>>Glycosphingolipid biosynthesis - globo and isoglobo series;>>Glycosphingolipid biosynthesis - ganglio series;>>Metabolic pathways;>>Lysosome
Gene nameHEXA
Protein nameBeta-hexosaminidase subunit alpha
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID15211
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP29416
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID300757
Rat gene linkView Rat Gene
Rat Swiss-ProtQ641X3
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from HEXA . at AA range: 121-170
SpecificityHEXA Polyclonal Antibody detects endogenous levels of HEXA protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)60kD
BackgroundThis 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. [provided by RefSeq, Jan 2016],
Functioncatalytic activity:Hydrolysis of terminal non-reducing N-acetyl-D-hexosamine residues in N-acetyl-beta-D-hexosaminides.,disease:Defects in HEXA are the cause of GM2-gangliosidosis type 1 (GM2G1) [MIM:272800]; also known as Tay-Sachs disease. GM2-gangliosidosis is an autosomal recessive lysosomal storage disease marked by the accumulation of GM2 gangliosides in the neuronal cells. GM2G1 is characterized by GM2 gangliosides accumulation in the absence of HEXA activity, leading to neurodegeneration and, in the infantile form, death in early childhood. GM2G1 has an increased incidence among Ashkenazi Jews and French Canadians in eastern Quebec. It exists in several forms: infantile (most common and most severe), juvenile and adult (late onset).,function:Responsible for the degradation of GM2 gangliosides, and a variety of other molecules containing terminal N-acetyl hexosamines, in the brain
Subcellular locationLysosome.
ExpressionBrain,Eye,Liver,Ovary,Uterus,

Additional Images

Image 1
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Western Blot analysis of HepG2 cells using HEXA Polyclonal Antibody. Antibody was diluted at 1:1000. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded rat-brain, antibody was diluted at 1:100
: AO-06-ES3963-100
: 10 Produits
Hurry! only 10 items left in stock.

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