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Fitc annexin 5 propidium iodide apoptosis detection kit 1

Manufactured by BD
Sourced in United States

The FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I is a laboratory tool used to identify and quantify apoptosis, a type of programmed cell death. The kit contains FITC-labeled Annexin V and propidium iodide, which are used as fluorescent markers to detect phosphatidylserine exposure and cell membrane integrity, respectively.

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15 protocols using fitc annexin 5 propidium iodide apoptosis detection kit 1

1

Cell Proliferation and Apoptosis Assay

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Cell proliferation was measured by using the WST-1 assays (Roche) according to the manufacturers’ instructions. Flow cytometry was used for quantitative assessment of apoptosis using the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen).
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2

Cell Proliferation and Apoptosis Assays

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Cell proliferation was measured by using the WST-1 assays (Roche, Indianapolis, Indiana, USA) according to the manufacturers’ instructions. Flow cytometry was used for quantitative assessment of apoptosis with the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen, San Jose, California, USA).
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3

Cell Viability and Apoptosis Assays

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Cell viability was assessed using MTT assays for assessment of proliferative capacity, and flow cytometry for quantitative assessment of apoptosis. The standard MTT assays were performed as described previously [9 (link)]. For flow cytometry, the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen) were used according to the manufacturer’s instructions.
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4

Quantifying Cell Cycle and Apoptosis

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Flow cytometry was used for the quantitative assessment of cell cycle and apoptosis [44 (link)]. Briefly, to measure cell cycle response, PEL cell pellets were fixed in 70% ethanol, and incubated at 4°C overnight. Cell pellets were re-suspended in 0.5 mL of 0.05 mg/mL PI plus 0.2 mg/mL RNaseA, and incubated at 37°C for 30 min. Cell cycle distribution was analyzed using a BD Accuri C6 flow cytometer. Apoptosis was assessed by the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen, San Jose, California, USA) on a flow cytometer. Data was normalized as the fold change compared to the DMSO control.
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5

Cell Proliferation and Apoptosis Assay

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Cell proliferation was measured using the WST-1 assays (Roche, Indianapolis, Indiana, USA) according to the manufacturer’s instructions. Flow cytometry was used for quantitative assessment of apoptosis with the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen, San Jose, California, USA).
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6

Cell Proliferation and Apoptosis Assay

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MTT assays were used for assessment of proliferative capacity as described previously [47] (link). Flow cytometry was used for quantitative assessment of apoptosis using the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen) according to the manufacturer’s instructions.
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7

Apoptosis Quantification by Flow Cytometry

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Apoptosis was quantified by flow cytometry using the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen) according to the manufacturer's instructions. Data were collected using a FACS Calibur 4-color flow cytometer (BD Bioscience).
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8

Quantifying Apoptosis and Cell Cycle

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Flow cytometry was used for the quantitative assessment of apoptosis with the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen) analyzed on a FACS Calibur 4-color flow cytometer (BD Bioscience). For cell cycle analysis, DIPG pellets were fixed in 70% ethanol, and incubated at 4°C overnight. Cell pellets were re-suspended in 0.5 mL of 0.05 mg/mL PI plus 0.2 mg/mL RNaseA and incubated at 37°C for 30 min prior to FACS analysis.
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9

Cell Proliferation and Apoptosis Analysis

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Cell proliferation was determined by using the WST-1 assays (Roche) according to the manufacturer's instructions. Briefly, after the period of treatment of cells, 10 μL/well of cell proliferation reagent, WST-1 (4-[3-(4-Iodophenyl)-2-(4-nitro-phenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate), was added into 96-well microplate and incubated for 3 h at 37 °C in 5% CO2. The absorbance of samples was measured by using a microplate reader at 490 nm. Flow cytometry was used to the quantitative analysis of apoptosis with the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen).
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10

Cell Viability and Apoptosis Analysis

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Cell viability was assessed using MTT assays for assessment of proliferative capacity, and flow cytometry was used for quantitative assessment of apoptosis. Standard MTT assays were performed as described previously [5 (link)]. For flow cytometry, the FITC-Annexin V/propidium iodide (PI) Apoptosis Detection Kit I (BD Pharmingen) was used according to the manufacturer's instructions.
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