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Huntingtin pS13 antibody
Huntington disease protein (HD protein)
Gene name : HTT, HD, IT15
Gene name : HTT, HD, IT15
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00012853
Defects in HTT are the cause of Huntington disease (HD). HD is an autosomal dominant neurodegenerative disorder characterized by involuntary movements (chorea), general motor impairment, psychiatric disorders and dementia.
| ID Covalab | pab0870-IP |
|---|---|
| Product type | Primary antibodies |
| Clonality | Polyclonal antibody |
| Raised in | Rabbit |
| Immunogen | synthetic peptide derived from N terminal part of human Huntingtin containing a phospho serine at position 13 |
| Activity cross reaction | Reacts with the human 347 kDa Huntingtin pS13 protein. Cross react with mouse and rat protein due to sequence homology. |
| Species | Hu, Ms, Rat |
| Labelling | None |
| Form | Antigen affinity purified |
| Preservative | 0.02% NaN3 |
| Storage instructions | For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt. |
| Target | Huntingtin pS13 |
| Uniprot ID | P42858 |
| Applications | ELISA, IHC, WB |
| Working dilutions | Optimal dilutions should be determined by the end user. |
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