Tau-Tubulin Kinase 2 (TTBK2) Antibody
377€ (100 µg)
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935106861
info@markelab.com
name
Tau-Tubulin Kinase 2 (TTBK2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx239076
tested applications
ELISA, WB, IHC
Description
TTBK2 Antibody is a Rabbit Polyclonal against TTBK2.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Target: Tau-Tubulin Kinase 2 (TTBK2) Immunogen: tau tubulin kinase 2 |
| Host | Rabbit |
| Reactivity | Human, Rat |
| Assay Type | Concentration: 2 mg/ml |
| Recommended Dilution | WB: 1/500 - 1/2000, IHC: 1/50 - 1/200. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | Observed MW: 137 kDa |
| Purity | ≥ 95% (SDS-PAGE) |
| Purification | Purified by immunogen affinity chromatography. |
| Size 1 | 100 µg |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | PBS, pH 7.3, with 0.02% sodium azide and 50% glycerol. |
| Availability | Shipped within 5-12 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q6IQ55 |
| Background | Antibody anti-TTBK2 |
| Status | RUO |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |
Descripción
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TTBK2 antibody
This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.
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Tau-Tubulin Kinase 2 (TTBK2) Antibody
TTBK2 Antibody is a Rabbit Polyclonal Antibody against TTBK2.
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Tau-Tubulin Kinase 2 (TTBK2) Antibody
This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11) ; a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.
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