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Huntingtin antibody
Huntington disease protein (HD protein)
Gene name : HTT, HD, IT15
Gene name : HTT, HD, IT15
As low as
€294.00
In stock
Ref
00012849
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 | pab0869-P |
|---|---|
| Product type | Primary antibodies |
| Clonality | Polyclonal antibody |
| Raised in | Rabbit |
| Immunogen | synthetic peptide derived from N terminal part of human Huntingtin |
| Activity cross reaction | Reacts with the human Huntingtin protein. Cross react with mouse and rat protein due to sequence homology. |
| Species | Hu, Ms, Rat |
| Labelling | None |
| Form | Purified (protein A) |
| Preservative | None |
| Storage instructions | Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt. |
| Target | Huntingtin |
| Uniprot ID | P42858 |
| Applications | ELISA, ICC, WB |
| Working dilutions | Optimal dilutions should be determined by the end user. |
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