CHMP2B Antibody (monoclonal) (M02)
Mouse monoclonal antibody raised against a full length recombinant CHMP2B.
|Calculated MW||23907 Da|
|Other Names||Charged multivesicular body protein 2b, CHMP25, Chromatin-modifying protein 2b, CHMP2b, Vacuolar protein sorting-associated protein 2-2, Vps2-2, hVps2-2, CHMP2B|
|Target/Specificity||CHMP2B (AAH01553.1, 1 a.a. ~ 213 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.|
|Format||Clear, colorless solution in phosphate buffered saline, pH 7.2 .|
|Storage||Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.|
|Precautions||CHMP2B Antibody (monoclonal) (M02) is for research use only and not for use in diagnostic or therapeutic procedures.|
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abgent to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
firstname.lastname@example.org, and receive a free "I Love Antibodies" mug.
Provided below are standard protocols that you may find useful for product applications.
This gene encodes a component of the heteromeric ESCRT-III complex (Endosomal Sorting Complex Required for Transport III) that functions in the recycling or degradation of cell surface receptors. ESCRT-III functions in the concentration and invagination of ubiquitinated endosomal cargos into intralumenal vesicles. The protein encoded by this gene is found as a monomer in the cytosol or as an oligomer in ESCRT-III complexes on endosomal membranes. It is expressed in neurons of all major regions of the brain. Mutations in this gene result in one form of familial frontotemporal lobar degeneration.
CHMP2B mutations are rare in French families with frontotemporal lobar degeneration. Ghanim M, et al. J Neurol, 2010 Jul 14. PMID 20625756.FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS. Tsai CP, et al. Neurobiol Aging, 2010 May 14. PMID 20472325.Immunopositivity for ESCRT-III subunit CHMP2B in granulovacuolar degeneration of neurons in the Alzheimer's disease hippocampus. Yamazaki Y, et al. Neurosci Lett, 2010 Jun 21. PMID 20420883.Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients. Kaivorinne AL, et al. Eur J Neurol, 2010 Apr 20. PMID 20412296.Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS). Cox LE, et al. PLoS One, 2010 Mar 24. PMID 20352044.
If you have used an Abgent product and would like to share how it has performed, please click on the "Submit Review" button and provide the requested information. Our staff will examine and post your review and contact you if needed.
If you have any additional inquiries please email technical services at email@example.com.