Cat. #151320
Anti-Spastin [Sp 3G11/1]
Cat. #: 151320
Sub-type: Primary antibody
Unit size: 100 ug
Availability: 1-2 weeks
Target: Spastin
Class: Monoclonal
Application: WB ; ChIP ; ELISA ; IHC ; IF ; WB
Reactivity: Human ; Mouse ; Rat
Host: Mouse
£300.00
This fee is applicable only for non-profit organisations. If you are a for-profit organisation or a researcher working on commercially-sponsored academic research, you will need to contact our licensing team for a commercial use license.
Contributor
Inventor: Giampietro Schiavo
Institute: Cancer Research UK, London Research Institute: Lincoln's Inn Fields
Tool Details
*FOR RESEARCH USE ONLY (for other uses, please contact the licensing team)
- Name: Anti-Spastin [Sp 3G11/1]
- Research fields: Cell biology;Cell signaling and signal transduction;Genetics;Metabolism;Neurobiology;Tissue-specific biology
- Clone: Sp 3G11/1
- Tool sub type: Primary antibody
- Class: Monoclonal
- Conjugation: Unconjugated
- Molecular weight: 52 kDa
- Strain: Balb/c
- Reactivity: Human ; Mouse ; Rat
- Host: Mouse
- Application: WB ; ChIP ; ELISA ; IHC ; IF ; WB
- Description: Spastin is thought have a role in microtubule dynamics through its function as a microtubule-severing protein. It is localised to the centrosome of neuronal cells but is not found in glial cells. Mutation in the ATPase binding domain of spastin causes hereditary spastic paraplegias (HSP), a large group of clinically similar disorders. Mutant forms of spastin are generally found throughout the cytoplasm rather then within the nucleus. There are two splice isoforms of spastin (one without exon4) and two alternative ATG start sites, which may determine the localisation of the translate protein.
- Immunogen: Recombinant human spastin
- Isotype: IgG2a
- Myeloma used: Sp2/0-Ag14
- Recommended controls: HeLa cell or rat brain extract
Target Details
- Target: Spastin
- Molecular weight: 52 kDa
- Tissue cell line specificity: HeLa cell or rat brain extract
- Target background: Spastin is thought have a role in microtubule dynamics through its function as a microtubule-severing protein. It is localised to the centrosome of neuronal cells but is not found in glial cells. Mutation in the ATPase binding domain of spastin causes hereditary spastic paraplegias (HSP), a large group of clinically similar disorders. Mutant forms of spastin are generally found throughout the cytoplasm rather then within the nucleus. There are two splice isoforms of spastin (one without exon4) and two alternative ATG start sites, which may determine the localisation of the translate protein.
Applications
- Application: WB ; ChIP ; ELISA ; IHC ; IF ; WB
Handling
- Format: Liquid
- Concentration: 1 mg/ml
- Unit size: 100 ug
- Storage buffer: PBS with 0.02% azide
- Storage conditions: -15° C to -25° C
- Shipping conditions: Shipping at 4° C
References
- Daftary et al. 2011. Mol Endocrinol. 25(9):1539-49. PMID: 21757506.
- A novel role for the AAA ATPase spastin as a HOXA10 transcriptional corepressor in Ishikawa endometrial cells.
- Lacroix et al. 2010. J Cell Biol. 189(6):945-54. PMID: 20530212.
- Lacroix et al. 2010. J Cell Biol. 189(6):945-54. PMID: 20530212.
- Tubulin polyglutamylation stimulates spastin-mediated microtubule severing.
- Salinas et al. 2005. J Neurochem. 95(5):1411-20. PMID: 16219033.
- Human spastin has multiple microtubule-related functions.