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Apoptag red detection kit

Manufactured by Merck Group

The ApopTag Red detection kit is a laboratory product designed to detect and visualize apoptosis, a form of programmed cell death, in cell samples. The kit utilizes an enzymatic process to label and identify DNA fragmentation, a hallmark of apoptosis. The resulting red-colored signal allows for the quantification and analysis of apoptotic cells.

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4 protocols using apoptag red detection kit

1

Apoptosis Detection in Breast Cancer Cells

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For TUNEL assay, MCF7 and T47D cells were cultured on glass coverslips. Cells were fixed, permeabilized and TUNEL assay was performed using the ApopTag Red detection kit (Chemicon, Inc.) following manufacturer's protocol. Samples were counterstained with DAPI before mounting. Cells were visualized using fluorescent microscopy.
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2

Apoptosis Detection in Breast Cancer Cells

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For TUNEL assay, MCF7 and T47D cells were cultured on glass coverslips. Cells were fixed, permeabilized and TUNEL assay was performed using the ApopTag Red detection kit (Chemicon, Inc.) following manufacturer's protocol. Samples were counterstained with DAPI before mounting. Cells were visualized using fluorescent microscopy.
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3

TUNEL Assay and MPO Activity Quantification

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TUNEL assay was performed using ApopTag Red detection kit (Millipore) according to manufacturer’s protocol. Four randomly selected high-power microscopic fields of each sample were examined using Leica DM 4000B microscope mounted with QI Click digital CCD camera. Number of TUNEL-positive cells were scored and normalized by total number of cells. MPO activity was measured as previous described50 (link). Enzymatic activity was measured at 450 nm using 96-well Multiskan microplate reader and determined from a standard curve generated by a serial dilution of purified MPO enzyme (Enzo Life Sciences).
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4

TUNEL Assay and MPO Activity Quantification

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TUNEL assay was performed using ApopTag Red detection kit (Millipore) according to manufacturer’s protocol. Four randomly selected high-power microscopic fields of each sample were examined using Leica DM 4000B microscope mounted with QI Click digital CCD camera. Number of TUNEL-positive cells were scored and normalized by total number of cells. MPO activity was measured as previous described50 (link). Enzymatic activity was measured at 450 nm using 96-well Multiskan microplate reader and determined from a standard curve generated by a serial dilution of purified MPO enzyme (Enzo Life Sciences).
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