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CHMP3 encodes a protein that sorts transmembrane proteins into lysosomes/vacuoles via the multivesicular body (MVB) pathway. Additionally we are shipping CHMP3 Antibodies (23) and many more products for this protein.
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Protein kinase CK2 (show CSNK2A1 Proteins) alpha (show CSNK2A2 Proteins) is involved in the phosphorylation of the ESCRT-III subunits CHMP3 and CHMP2B (show CHMP2B Proteins), as well as of VPS4B/SKD1 (show vps4b Proteins), an ATPase that mediates ESCRT-III disassembly.
tight coupling of ESCRT-III CHMP3 and AMSH (show STAMBP Proteins) functions and provide insight into the regulation of ESCRT-III
data suggest that mac25/IGFBP-rP1 (show IGFBP7 Proteins) and 25.1 (NEDF) may play a functional role in the NE differentiation of NSCLC cell lines and may provide a novel therapeutic target for treating lung cancers, in particular NSCLC with NE differentiation
ESCRT subunit is important for degradation of the epidermal growth factor receptor (EGFR (show EGFR Proteins)) and for transport of the receptor from endosomes to lysosomes.
A dominant-negative version of CHMP3, which specifically prevents targeting of AMSH (STAMBP (show STAMBP Proteins)) to endosomes, inhibits degradation but not internalization of epidermal growth factor receptor (show EGFR Proteins).
Data demonstrate that the VPS24 gene gives rise to two functionally distinct proteins, one of which is involved in the ESCRT pathway and another novel protein that serves an anti-apoptotic role.
expression of dominant negative forms of Vps4 (show VPS4A Proteins) and Vps24, two components of the MVB pathway, rresult in an impairment in infectious herpes simplex virus assembly/egress
UBPY (show USP8 Proteins) MIT domain and another ubiquitin isopeptidase, AMSH (show STAMBP Proteins), reveals common interactions with CHMP1A (show CHMP1A Proteins) and CHMP1B but a distinct selectivity of AMSH (show STAMBP Proteins) for CHMP3/VPS24, a core subunit of the ESCRT-III complex, and UBPY (show USP8 Proteins) for CHMP7 (show CHMP7 Proteins).
study found the ESCRT-III proteins CHMP2A (show CHMP2A Proteins) & CHMP3 could assemble in vitro into helical tubular structures that expose their membrane interaction sites on the outside of the tubule; VPS4 (show VPS4A Proteins) could bind on the inside of the tubule & disassemble the tubes
Data show that the N-terminal core domains of increased sodium tolerance-1 (IST1 (show IST1 Proteins)) and charged multivesicular body protein-3 (CHMP3) form equivalent four-helix bundles, revealing that IST1 (show IST1 Proteins) is a previously unrecognized ESCRT-III family member.
This gene encodes a protein that sorts transmembrane proteins into lysosomes/vacuoles via the multivesicular body (MVB) pathway. This protein, along with other soluble coiled-coil containing proteins, forms part of the ESCRT-III protein complex that binds to the endosomal membrane and recruits additional cofactors for protein sorting into the MVB. This protein may also co-immunoprecipitate with a member of the IFG-binding protein superfamily. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ring finger protein 103 (RNF103) gene.
charged multivesicular body protein 3
, chromatin-modifying protein 3
, vacuolar protein sorting 24 homolog
, vacuolar protein-sorting-associated protein 24
, Charged multivesicular body protein 3
, neuroendocrine differentiation factor
, vacuolar protein sorting-associated protein 24
, 25.1 protein
, CHMP family, member 3
, vacuolar protein sorting 24
, Vps24p protein