Huntingtin (HTT) Antibody
442€ (100 µg)
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name
Huntingtin (HTT) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx461530
tested applications
ELISA, SPR
Description
Huntingtin (HTT) Antibody is a monoclonal Nanobody expressed in CHO cells for the detection of Human HTT.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Huntingtin (HTT) |
| Host | CHO cells |
| Reactivity | Human |
| Clonality | Monoclonal |
| Conjugation | Unconjugated |
| Isotype | VHH-8His-Cys-tag |
| Clone ID | A504 |
| Purity | > 95% (SDS-PAGE) |
| Purification | Purified by Protein A/G affinity chromatography. |
| Size 1 | 100 µg |
| Size 2 | 1 mg |
| Form | Liquid |
| Tested Applications | ELISA, SPR |
| Buffer | 0.01 M PBS, pH 7.4. |
| Availability | Shipped within 5-12 working days. |
| Storage | Store at 4 °C if the entire vial will be used within 1 week. Aliquot and store at -20 °C or -80 °C for long-term storage. Avoid repeated freeze-thaw cycles. |
| Dry Ice | No |
| UniProt ID | P42858 |
| Gene ID | 3064 |
| NCBI Accession | NP_002102.4 |
| Background | Antibody anti-HTT |
| Status | RUO |
| Note | Concentration: 1 mg/ml - |
Descripción
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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.
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