HTT antibody

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935106861
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name
HTT antibody
category
Primary Antibodies
provider
FineTest
reference
FNab09844
tested applications
ELISA, IF, IHC
Description
HTT(huntingtin), also named as HD and IT15, belongs to the huntingtin family. HTT may play a role in microtubule-mediated transport or vesicle function. Defects in HTT are the cause of Huntington disease (HD) which is an autosomal dominant neurodegenerative disorder characterized by involuntary movements (chorea), general motor impairment, psychiatric disorders and dementia.
Documents del producto
Product specifications
Category | Primary Antibodies |
Immunogen Target | Huntingtin (HTT) |
Host | Rabbit |
Reactivity | Human, Mouse |
Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50-1:500; IF: 1:50-1:500 |
Clonality | polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Observed MW | 348 kDa |
Purity | ≥95% as determined by SDS-PAGE |
Purification | Immunogen affinity purified |
Size 1 | 100µg |
Form | liquid |
Tested Applications | ELISA, IF, IHC |
Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
UniProt ID | P42858 |
Gene ID | 3064 |
Alias | Huntingtin,Huntington disease protein (HD protein),Huntingtin, myristoylated N-terminal fragment,HTT,HD,IT15 |
Background | Antibody anti-HTT |
Status | RUO |
Note | Mol. Weight 348 kDa |
Descripción
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HTT antibody
HTT(huntingtin), also named as HD and IT15, belongs to the huntingtin family. HTT may play a role in microtubule-mediated transport or vesicle function. Defects in HTT are the cause of Huntington disease (HD) which is an autosomal dominant neurodegenerative disorder characterized by involuntary movements (chorea), general motor impairment, psychiatric disorders and dementia.
Ver Producto