Tau-Tubulin Kinase 2 (TTBK2) Antibody
286€ (100 µl)
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935106861
info@markelab.com
name
Tau-Tubulin Kinase 2 (TTBK2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx129224
tested applications
WB, IHC, IF/ICC
Description
Tau-Tubulin Kinase 2 Antibody is a Rabbit Polyclonal against Tau-Tubulin Kinase 2.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Target: Tau-Tubulin Kinase 2 (TTBK2) Immunogen: tTBK2 (Trp21-Thr314) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | WB: 0.01-2 µg/ml, IHC: 5-20 µg/ml, IF/ICC: 5-20 µg/ml. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Purification | Purified by antigen-specific affinity chromatography, followed by Protein A affinity chromatography. |
| Size 1 | 100 µl |
| Size 2 | 200 µl |
| Size 3 | 1 ml |
| Form | Liquid |
| Tested Applications | WB, IHC, IF/ICC |
| Buffer | 0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol. |
| Availability | Shipped within 5-7 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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