HEXB Rabbit Polyclonal Antibody
CNY 1350.00
货期*
2周
规格
Specifications
| Product Data | |
| Applications | WB |
| Recommend Dilution | WB: 1:500~1:1000 IHC: 1:50~1:200 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide, corresponding to amino acids 481-530 of Human Hexb. |
| Specificity | Hexb (S516) polyclonal antibody detects endogenous levels of Hexb protein. |
| Isotype | IgG |
| Formulation | Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2 |
| Concentration | 1mg/ml |
| Conjugation | Unconjugated |
| Storage Condition | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles. |
| Predicted Protein Size | ~ 63 kDa |
| Gene Name | hexosaminidase subunit beta |
| Database Link | |
| Background | Hexosaminidase B (HEXB), also designated beta-hexosaminidase B, is a Hexosaminidase B (HEXB), also designated b-hexosaminidase B, is a tetramer of two b-A and two b-B chains and is found in the lysosomes of cells. Sandhoff disease (SD), also known as GM2-gangliosidosis type II, is caused by mutations in the HEXB gene that affect the b subunit. These mutations disrupt the activity of HEXB and HEXA, which prevents the breakdown of GM2 ganglioside, a fatty material found in the brain, therby rendering both the HEXA and HEXB enzymes deficient. SD is a rare autosomal recessive disorder characterized by an accumulation of GM2 ganglioside, which causes progressive destruction of the central nervous system. Sandhoff disease is similar to Tay-Sachs disease, which is caused by mutations in the HEXA gene, although SD is more severe. |
| Synonyms | Beta-hexosaminidase subunit beta; Beta-N-acetylhexosaminidase subunit beta; Cervical cancer proto-oncogene 7 protein; HCC-7; HCC7; HEXB; Hexosaminidase subunit B; N-acetyl-beta-glucosaminidase subunit beta |
| Note | For research use only, not for use in diagnostic procedure. |
| Reference Data | |
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