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11772457001

Roche

TUNEL AP

sufficient for 70 tests, solution, pkg of 3.5 mL

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About This Item

Code UNSPSC :
41105600

Forme

solution

Utilisation

sufficient for 70 tests

Conditionnement

pkg of 3.5 mL

Fabricant/nom de marque

Roche

Conditions d'expédition

wet ice

Température de stockage

2-8°C

Description générale

TUNEL AP is an alkaline phosphatase-labeled antibody used for the in situ detection of apoptosis (programmed cell death) with the TUNEL reaction followed by transmission light microscopy.
The tailing reaction using TdT, also named ISEL (in situ end labeling) or TUNEL (TdT-mediated dUTP nick end labeling), has several advantages in comparison to the in situ nick translation (ISNT) using DNA polymerase:
  • Label intensity of apoptotic cells is higher with TUNEL compared to ISNT, resulting in an increased sensitivity.
  • Kinetics of nucleotide incorporation is very rapid with TUNEL compared to the ISNT.
  • TUNEL preferentially labels apoptotic cells compared to necrotic cells.

Application

TUNEL AP is an antibody that is used to convert fluorescence-based TUNEL assays into colorimetric assays suited for light microscopy. The conversion is performed by binding of an anti-fluorescein antibody to FITC-dUTP. The antibody is labeled with alkaline phosphatase (AP). The AP is visualized with a precipitating substrate, such as Fast Red or NBT/BCIP.

Composants

Anti-fluorescein antibody, Fab fragment from sheep, conjugated with alkaline phosphatase (AP). Ready-to-use solution.

Autres remarques

For life science research only. Not for use in diagnostic procedures.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Skin Sens. 1

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

No data available

Point d'éclair (°C)

No data available


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The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 41(7), 1023-1030 (1993-07-01)
Since DNA fragmentation is a key feature of programmed cell death (PCD) and also occurs in certain stages of necrosis, we have adapted the methodology of in situ nick-translation (ISNT) to detect DNA fragmentation on a single-cell level. We first
W Gorczyca et al.
Cytometry, 15(2), 169-175 (1994-02-01)
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