Anti-ANO5/TMEM16E Antibody (N421A/85)

Our Anti-ANO5/TMEM16E mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N421A/85. It detects human ANO5/TMEM16E, and is purified by Protein A chromatography. It is great for use in ICC, WB.



SKU: 75-410

Volume: 100 µL
1-2 business days
Price:
Sale price$374.00

Product Specific References for Applications and Species

Immunocytochemistry: Human
PMID Dilution Publication
296653211:100Xu, 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
28489263not listedVihola, 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
36951953not listedSchmaier, A.A., et al. 2023. TMEM16E regulates endothelial cell procoagulant activity and thrombosis. Journal of Clinical Investigation, e163808.
36292621not listedSoontrapa, P., et al. 2022. Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review. Genes (Basel), 1736.
349634851:1000Li, 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.
29665321not listedXu, 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.
28489263not listedVihola, 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
269116751:100Griffin, 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
33818761Mavillard, F., et al. 2021. Novel ANO5 intronic Roma variant alters splicing causing muscular dystrophy. Clinical Genetics, 106-110.

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