Cell Signaling Technology

Product Pathways - Cell Cycle / Checkpoint

NuMA (D49H4) Rabbit mAb #8967

Applications Reactivity Sensitivity MW (kDa) Isotype
W IF-IC H Mk Endogenous 238 Rabbit IgG

Applications Key:  W=Western Blotting  IF-IC=Immunofluorescence (Immunocytochemistry)
Reactivity Key:  H=Human  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

NuMA (D49H4) Rabbit mAb detects endogenous levels of total NuMA protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human NuMA protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines using NuMA (D49H4) Rabbit mAb.

IF-IC

IF-IC

Confocal immunofluorescent analysis of MCF7 cells using NuMA (D49H4) Rabbit mAb (green). Actin filaments were labeled with DY-554 phalloidin (red). Blue pseudocolor= DRAQ5® #4084 (fluorescent DNA dye).

Background

The nuclear mitotic apparatus protein (NuMA) is a coiled coil protein involved in the formation and maintenance of the mitotic spindle. NuMA plays a role in chromatin organization during interphase, which influences mammary epithelial differentiation (1,2). During apoptosis, carboxy-terminal cleavage of NuMA may amplify signaling in the cell death pathway (2). NuMA is phosphorylated at numerous sites, with phosphorylation at Ser395 occurring in an ATM/ATR-dependent manner in response to DNA damage (3,4).

  1. Abad, P.C. et al. (2007) Mol Biol Cell 18, 348-61.
  2. Lin, H.H. et al. (2007) J Biomed Sci 14, 681-94.
  3. Stokes, M.P. et al. (2007) Proc Natl Acad Sci USA 104, 19855-60.
  4. Matsuoka, S. et al. (2007) Science 316, 1160-6.

Application References

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Companion Products


For Research Use Only. Not For Use In Diagnostic Procedures.

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