R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
CENP-F (D6X4L) Rabbit mAb #58982
Filter:
- WB
- IF
- F
Supporting Data
REACTIVITY | H |
SENSITIVITY | Endogenous |
MW (kDa) | 450 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IF-Immunofluorescence
- F-Flow Cytometry
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunofluorescence (Immunocytochemistry) | 1:800 |
Flow Cytometry (Fixed/Permeabilized) | 1:50 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
CENP-F (D6X4L) Rabbit mAb recognizes endogenous levels of total CENP-F protein.
Species Reactivity:
Human
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala1794 of human CENP-F protein.
Background
CENP-F (mitosin), is a kinetochore-associated protein whose expression and localization to chromatin is regulated in a cell cycle-dependent manner, with its highest expression in G2/M phases (1, 2). CENP-F is required for appropriate localization of other kinetocore-associated proteins, including CENP-E. CENP-F regulates kinetocore function and maintenance of the mitotic spindle checkpoint. Farnesylation of CENP-F is required for its localization and function (3). CENP-F also interacts with the mitochondrial protein, miro, to direct the distribution of mitochondria to daughter cells as they exit mitosis (4). Researchers have shown that CENP-F drives prostate tumor growth synergistically with FOXM1 in human and mouse (5), and that the gene for CENP-F is among those frequently amplified in hepatocellular, head and neck, and esophageal carcinomas (6-8). CENP-F expression has also been shown in research studies to be associated with poor prognosis in breast cancer (9).
- Rattner, J.B. et al. (1993) Cell Motil Cytoskeleton 26, 214-26.
- Liao, H. et al. (1995) J Cell Biol 130, 507-18.
- Ma, L. et al. (2006) J Biomed Sci 13, 205-13.
- Kanfer, G. et al. (2015) Nat Commun 6, 8015.
- Aytes, A. et al. (2014) Cancer Cell 25, 638-51.
- Kim, H.E. et al. (2012) PLoS One 7, e43223.
- Pimkhaokham, A. et al. (2000) Jpn J Cancer Res 91, 1126-33.
- de la Guardia, C. et al. (2001) Head Neck 23, 104-12.
- O'Brien, S.L. et al. (2007) Int J Cancer 120, 1434-43.
限制使用
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For Research Use Only. Not For Use In Diagnostic Procedures.
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