Product Pathways - Cell Cycle / Checkpoint
CHFR (D40H6) Rabbit mAb #6904
PhosphoSitePlus® protein, site, and accession data: CHFR
| Applications | Reactivity | Sensitivity | MW (kDa) | Isotype |
|---|---|---|---|---|
| W IP | H M R Mk | Endogenous | 80 | Rabbit IgG |
Applications Key:
W=Western Blotting
IP=Immunoprecipitation
Reactivity Key:
H=Human
M=Mouse
R=Rat
Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
Protocols
Specificity / Sensitivity
CHFR (D40H6) Rabbit mAb recognizes endogenous levels of total CHFR protein.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Lys612 of human CHFR protein.
Western Blotting
Western blot analysis of MDA-MB-231 cells untreated (-) or nocodazole-treated (+) using CHFR (D40H6) Rabbit mAb.
Western Blotting
Western blot analysis of extracts from various cell lines using CHFR (D40H6) Rabbit mAb.
Background
Checkpoint with forkhead and RING finger domains protein (CHFR) is an E3 ubiquitin-protein ligase that regulates cell cycle progression. In response to microtubule stress, CHFR delays the transition into mitosis by excluding cyclin B1 from the nucleus prior to chromosome condensation (1). Marked reduction of CHFR expression was detected in primary tumors and decreased CHFR expression was linked to promoter hypermethylation (1-4). Restoration of CHFR expression by treatment with the microtubule stress agent nocodazole and the methyltransferase inhibitor 5-aza-2'-deoxycytidine has been reported (4,5).
- Summers, M.K. et al. (2005) Oncogene 24, 2589-98.
- Privette, L.M. et al. (2007) Cancer Res 67, 6064-74.
- Morioka, Y. et al. (2006) Anticancer Res 26, 4267-70.
- Satoh, A. et al. (2003) Cancer Res 63, 8606-13.
- Dang, C. and Hudis, C. (2006) Clin Breast Cancer 7, 51-8.
Application References
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For Research Use Only. Not For Use In Diagnostic Procedures.
