Caspases are key effectors of programmed cell death. They are synthesized as inactive proenzymes which are activated by cleavage at a specific aspartate residue to form two subunits. These subunits are normally linked together by a linker which may be in
Provided as solution in phosphate buffered saline with 0.08% sodium azide
Purity:
Protein A/G Chromatography
Formula:
Provided as solution in phosphate buffered saline with 0.08% sodium azide
Application Notes:
Detects proenzyme form of human Caspase-9 by Western blot analysis as well as one of the cleavage products after treatment with thapsigargin. Optimal concentration should be evaluated by serial dilutions.
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