HEXA Mouse Monoclonal Antibody [Clone ID: 3F10]
CAT#: AM06756PU-N
HEXA mouse monoclonal antibody, clone 3F10, Purified
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CNY 5,775.00
货期*
5周
规格
Specifications
Product Data | |
Clone Name | 3F10 |
Applications | ELISA, FC, WB |
Recommend Dilution | ELISA: 1/10000. Western Blot: 1/500 - 1/2000. Flow Cytometry: 1/200 - 1/400. |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Purified recombinant fragment of Human HEXA expressed in E. Coli. |
Specificity | Recognizes Beta-hexosaminidase alpha / HEXA |
Formulation | PBS State: Purified State: Liquid purified antibody Stabilizer: 0.5% protein stabilizer Preservative: 0.05% Sodium Azide |
Concentration | lot specific |
Conjugation | Unconjugated |
Storage Condition | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Predicted Protein Size | 60.7 kDa |
Gene Name | hexosaminidase subunit alpha |
Database Link | |
Background | 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). |
Synonyms | beta-N-acetylhexosaminidase; MGC99608; N-acetyl-beta-glucosaminidase; TSD |
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