#151827

Anti-Phospho CHMP4C [pCHMP4C]

Cat. #151827

Anti-Phospho CHMP4C [pCHMP4C]

Cat. #: 151827

Unit size: 100 ug

Availability: 10-12 weeks

Target: Phospho charged multi vesicular protein 4c

Class: Polyclonal

Application: WB

Reactivity: Mammalian

Host: Rabbit

£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: P Paolo D'Avino

Institute: University of Cambridge

Primary Citation: Capalbo et al. 2012. Open Biol. 2:120070 PMID: 22724069

Tool Details
Target Details
Applications
Handling
References

Tool Details

*FOR RESEARCH USE ONLY

  • Name: Anti-Phospho CHMP4C [pCHMP4C]
  • Clone: pCHMP4C
  • Class: Polyclonal
  • Conjugation: Unconjugated
  • Molecular weight: ~30
  • Reactivity: Mammalian
  • Host: Rabbit
  • Application: WB
  • Description: Borealin interacts directly with Snf7/Shrb/CHMP4 components in both Drosophila and human cells and the two proteins colocalize at the midbody in late cytokinesis. Aurora B phosphorylates CHMP4C at three serine residues located in its C-terminal linker region, a part of the protein known to regulate its ability to form polymers and interact with the membrane. Over-expression of CHMP4C variants mutated in these three residues caused cytokinesis failure, suggesting that Aurora B inhibits CHMP4C activity during cytokinesis. It is proposed that CPC controls abscission timing in both flies and human cells by regulating the function of ESCRT-III Snf7 proteins during cytokinesis through the interaction of its Borealin component with the N-terminus of Shrb/CHMP4 proteins and Aurora B-mediated phosphorylation of the CHMP4C regulatory linker tail.
  • Immunogen: Synthetic peptide (TARRSRAASSQRAEEC)
  • Recommended controls: Synchronised HeLa cell extracts. Signals are absent in a twin blot that had been pre-incubated with lambda-phosphatase, indicating that the antibody specifically recognizes a phosphorylated form of CHMP4C.

Target Details

  • Target: Phospho charged multi vesicular protein 4c
  • Molecular weight: ~30
  • Target background: Borealin interacts directly with Snf7/Shrb/CHMP4 components in both Drosophila and human cells and the two proteins colocalize at the midbody in late cytokinesis. Aurora B phosphorylates CHMP4C at three serine residues located in its C-terminal linker region, a part of the protein known to regulate its ability to form polymers and interact with the membrane. Over-expression of CHMP4C variants mutated in these three residues caused cytokinesis failure, suggesting that Aurora B inhibits CHMP4C activity during cytokinesis. It is proposed that CPC controls abscission timing in both flies and human cells by regulating the function of ESCRT-III Snf7 proteins during cytokinesis through the interaction of its Borealin component with the N-terminus of Shrb/CHMP4 proteins and Aurora B-mediated phosphorylation of the CHMP4C regulatory linker tail.

Applications

  • Application: WB

Handling

  • Format: Liquid
  • Concentration: 0.9-1.1mg/ml
  • Unit size: 100 ug
  • Storage buffer: PBS with 0.02% azide
  • Storage conditions: -20° C
  • Shipping conditions: Shipping at 4° C

References

  • Capalbo et al. 2012. Open Biol. 2:120070 PMID: 22724069
  • Petsalaki et al. 2016. Nat Commun. 7:11451. PMID: 27126587.