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In Situ Cell Death Detection Kit

The In Situ Cell Death Detection Kit has been designed as a precise, fast, and simple non radioactive technique to detect and quantify apoptotic cell death at the single-cell level in tissues. It is based on the so-called TUNEL method.



During apoptosis, DNAse activity not only generates double-stranded, low-molecular-weight DNA fragments (mono- and oligonucleosomes), but also introduces strand breaks ("nicks") into the high-molecular-weight DNA. These processes can be identified by labeling the free 3-OH termini with terminal transferase (TdT), which attaches labeled nucleotides to all 3OH-ends (TUNEL reaction; TdT-mediated dUTP nick end labeling). This labeling is more sensitive than other methods, and is the method used by the Roche Applied Science In situ Cell Death Detection Kits. There are four different versions of this kit: In Situ Cell Death Detection Kit, Fluorescein; In Situ Cell Death Detection Kit, TMR red (tetramethylrhodamine red); In Situ Cell Death Detection Kit, AP (alkaline phosphatase); and In Situ Cell Death Detection Kit, POD (peroxidase).



This figure shows the detection principle of the TUNEL kits. Labeling with fluorescein may also be followed by immunohistochemical detection using anti-fluorescein-specific antibodies that are conjugated to POD or AP. Typical applications of the TUNEL kits are:
  • Detection of individual apoptotic cells in frozen and formalin-fixed tissue sections in basic research and routine pathology
  • Determination of the sensitivity of malignant cells to drug-induced apoptosis in cancer research
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Homo sapiens MEP50 protein, mRNA
Co-precipitant is free of background polynucleotides,Dnases,Rnases, proteases. 20mg/ml
Can be used for the quantitative recovery of small amounts of nucleic acids within dilute solutions. 5mg/ml
RAB32, member RAS oncogene family, mRNA (cDNA clone MGC:13500 IMAGE:4280407), complete cds
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