Primary Antibody
Human, Mouse
N421A/85
ICC, IHC, WB
Mouse
Purified by Protein A chromatography
ANO5 GDD1 TMEM16E
110 kDa
Immunoblot against extracts of COS cells transiently transfected with untagged ANO5/TMEM16E, GFP- tagged ANO6/TMEM16F or untagged Kv2.1 plasmid probed with N421A/85 (left) or N86/38 (right) TC supe.
Product Specific References for Applications and Species
- Immunocytochemistry: Human
- Immunohistochemistry: Human
- Western Blot: Human | Mouse
- Additional Publications: Unspecified
| Immunocytochemistry: Human | ||
| PMID | Dilution | Publication |
| 29665321 | 1:100 | Xu, J., et al. 2018. A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptide. Journal of Pathology, Clinical Research, 135-142. |
| Immunohistochemistry: Human | ||
| PMID | Dilution | Publication |
| 28489263 | not listed | Vihola, A., et al. 2017. Diagnostic anoctamin-5 protein defect in patients with ANO5-mutated muscular dystrophy.. Neuropathology and Applied Neurobiology, 441-448. |
| Western Blot: Human | ||
| PMID | Dilution | Publication |
| 36951953 | not listed | Schmaier, A.A., et al. 2023. TMEM16E regulates endothelial cell procoagulant activity and thrombosis. Journal of Clinical Investigation, e163808. |
| 36292621 | not listed | Soontrapa, P., et al. 2022. Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review. Genes (Basel), 1736. |
| 34963485 | 1:1000 | Li, H., et al. 2021. BVES is a novel interactor of ANO5 and regulates myoblast differentiation. Cell & bioscience, 11(1), pp.1-10.. Cell & Bioscience, 1-10. |
| 29665321 | not listed | Xu, J., et al. 2018. A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptide. Journal of Pathology, Clinical Research, 135-142. |
| 28489263 | not listed | Vihola, A., et al. 2017. Diagnostic anoctamin-5 protein defect in patients with ANO5-mutated muscular dystrophy.. Neuropathology and Applied Neurobiology, 441-448. |
| Western Blot: Mouse | ||
| PMID | Dilution | Publication |
| 26911675 | 1:100 | Griffin, D.A., et al. 2016. Defective membrane fusion and repair in Anoctamin5-deficient muscular dystrophy.. Human Molecular Genetics, 1900-1911. |
| Additional Publications: Unspecified | ||
| PMID | Publication | |
| 33818761 | Mavillard, F., et al. 2021. Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophy. Clinical Genetics, 106-110. | |