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- Additional protein information
- Analytical tools
PathScan® Apoptosis and Proliferation Multiplex IF Kit #7851
This product is discontinued
Gallery: PathScan® Apoptosis and Proliferation Multiplex IF Kit #7851
|Primary Cocktail||7847||100 µl||Immunofluorescence (Immunocytochemistry), |
|Detection Cocktail||7843||100 µl||Immunofluorescence (Immunocytochemistry), |
‡Immunofluorescence (Paraffin) protocol recommended unmasking buffer: Citrate
|Kit Analytes||Detection Dye||Ex(max) (nm)||Em(max) (nm)|
|Phospho-Histone H3 (Ser10)||Alexa Fluor® 488||495||519|
|Cleaved-PARP (Asp214)||Alexa Fluor® 647||650||665|
|α-Tubulin||Alexa Fluor® 555||555||565|
The PathScan® Apoptosis and Proliferation Multiplex IF kit offers a novel method to simultaneously monitor mitotic index and programmed cell death using manual immunofluorescence microscopy, or automated imaging and laser scanning high content platforms. This kit contains a cocktail of three high quality primary antibodies targeted against α-tubulin, phospho-histone H3 (Ser10), and cleaved PARP (Asp214), as well as a detection cocktail utilizing the Alexa Fluor® series of fluorescent dyes. Antibody and dye pairings have been pre-optimized, and each kit contains enough reagents for 100 assays (based on a working volume of 100 μL/test).
α-Tubulin antibody detects endogenous levels of total α-tubulin protein. Phospho-Histone H3 (Ser10) antibody detects endogenous levels of histone H3 only when phosphorylated at Ser10. This antibody does not cross-react with other phosphorylated or acetylated histones. Cleaved-PARP (Asp214) detects endogenous levels of the large fragment (89 kDa) of human PARP1 protein produced by caspase cleavage. This antibody does not recognize full length PARP1 or other PARP isoforms.
Monoclonal antibodies were produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser10 of human histone H3, a synthetic peptide corresponding to residues surrounding Asp213 of human PARP, or with full-length chicken α-tubulin purified from brain extracts.
Apoptosis is a regulated physiological process leading to cell death. Initiator caspases cleave and activate downstream effector caspases that in turn cleave cytoskeletal and nuclear proteins like PARP, α-fodrin, DFF, and lamin A, which induce apoptosis (1). Cleavage of the nuclear poly (ADP-ribose) polymerase PARP occurs between Asp214 and Gly215, which separates the PARP amino-terminal DNA binding domain (24 kDa) from the carboxy-terminal catalytic domain (89 kDa) (2,3). PARP helps to maintain cell viability by playing key roles in many cellular processes, including DNA replication, repair, and recombination. Cleavage of PARP facilitates cellular disassembly and serves as a marker of cells undergoing apoptosis (4). Cell proliferation can be measured by studying the phosphorylation state of histone H3 and microtubule assembly during mitosis. Histone H3 is one of four distinct core histone proteins found in the nucleosome. Phosphorylation of histone H3 at Ser10, Ser28, and Thr11 is tightly correlated with chromosome condensation during both mitosis and meiosis (5-7). Heterodimers composed of α-tubulin and β-tubulin form globular tubulin subunits common to all eukaryotic cells. Tubulin polymers known as microtubules are fundamental cytosolic fibers important in mediating cellular movement, including meiotic/mitotic chromosome alignment, cytoplasmic membrane vesicle transport, and nerve-cell axon migration (8).
For Research Use Only. Not For Use In Diagnostic Procedures. Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc. PathScan is a trademark of Cell Signaling Technology, Inc.