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Technical Resources
Technical Information
Calbiochem Information
Apoptosis Resource
Beginning of the End
Induction of Apoptosis
Changes at the Plasma Membrane
Changes in the Mitochondria
Changes in the Cytoplasm
Changes in the Nucleus
Measurement of Cell Proliferation
Appendix
Apoptosis Resource: Measurement of Cell Proliferation
 
Induction of Apoptosis
Measurement of Apoptosis-Induced Changes at the Plasma Membrane
Measurement of Apoptosis-Induced Changes in the Mitochondria
Measurement of Apoptosis-Induced Changes in the Cytoplasm
Measurement of Apoptosis-Induced Changes in the Nucleus
Measurement of Cell Proliferation
Appendix
Measurement of Cell Proliferation
In multicellular organisms, a delicate balance between cell proliferation and cell death is maintained for normal cellular homeostasis, failure of this balance can lead to disease states. For example, on an average day humans produce ~60 x 109 new cells and at the same time eliminate roughly the same number of mature cells. Hence, a coupled relationship exists between proliferation and apoptosis. While certain morphological and biochemical changes serve as markers of apoptosis, cell proliferation can be used as another criteria for assessing apoptosis. Incorporation of the thymidine analog, bromodeoxyuridine (BrdU), into newly synthesized DNA strands of actively proliferating cells can be used as an alternative to radioisotopic methods for measuring cell proliferation. Following partial denaturation of double-stranded DNA, BrdU is detected immunochemically using an anti-BrdU antibody, allowing the assessment of the population of cells, which are actively synthesizing DNA.
 

Reference:
Reed, J .C . 2002 . Nat. Rev. Drug Discov. 1, 111 .

 
Measurement of Cell Proliferation: Kits
 
 
BrdU Cell Proliferation Assay
Cat. No. QIA58

BrdU Cell Proliferation Assay is a non-isotopic immunoassay for quantification of BrdU incorporation into newly synthesized DNA of actively proliferating cells. It is sensitive, rapid, and easy to perform.