Cell Signaling Technology

Product Pathways - Apoptosis / Autophagy

Caspase-10 Antibody #9752

Applications Reactivity MW (kDa) Source
W H M R 63 to 66 Rabbit

Applications Key:  W=Western Blotting
Reactivity Key:  H=Human  M=Mouse  R=Rat
Species enclosed in parentheses are predicted to react based on 100% sequence homology. Species cross-reactivity is determined by Western blot.

Specificity / Sensitivity

Caspase-10 Antibody detects endogenous levels of full length caspase-10 and its various isoforms. The antibody does not cross-react with other caspases.

Source / Purification

Polyclonal antibodies are produced by immunizing rabbits with a synthetic peptide (KLH-coupled) corresponding to residues surrounding aspartic acid 219 of human caspase-10. Antibodies are purified by protein A and peptide affinity chromatography.

Western Blotting

Western Blotting

Western blot analysis of extracts from Jurkat, C6 and NIH/3T3 cells, untreated or cytochrome c-treated, using Caspase-10 Antibody.

Background

Caspase-10 is a DED (death effector domain)-containing caspase and functions as an initiator caspase in Fas/TNF induced apoptosis (1). Four isoforms of caspase-10 have been identified: caspase-10a (Mch4), caspase-10b (FLICE2), caspase-10c and caspase-10d. They have the same prodomain but different mature large and small subdomains (2-4). Upon death ligand-receptor binding, caspase-10 is coupled to the multimeric Fas/TNF receptor complex via DED/FADD adaptor interaction (1-4). This complex processes procaspase-10 into a large active fragment and a small fragment. Cleaved caspase-10 further processes other caspase members, including caspase-3 and caspase-7, to initiate a caspase cascade, leading to apoptosis (3-6).

  1. Nunez, G. et al. (1998) Oncogene 17, 3237-3245.
  2. Ng, P. W. et al. (1999) J. Biol. Chem. 274, 10301-10308.
  3. Vincenz, C. and Dixit, V.M. (1997) J. Biol. Chem. 272, 6578-6583.
  4. Fernandez-Alnemri, T. et al. (1996) Proc. Natl. Acad. Sci. USA 93, 7464-7469.
  5. Srinivasula, S. M. et al. (1996) Proc. Natl. Acad. Sci. USA 93, 14486-14491.
  6. Wang, J. et al. (1999) Cell 98, 47-58.

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