DNA Damage Assay Human bronchial epithelial cells (hBE)

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Get tips on using In Situ Cell Death Detection Kit, TMR red to perform TUNEL assay cell type - A127, U87MG, U251MG, T98G human glioblastoma cells

Products Sigma-Aldrich In Situ Cell Death Detection Kit, TMR red

Get tips on using ROS-Glo™ H2O2 Assay to perform ROS assay cell type - HEK293

Products Promega ROS-Glo™ H2O2 Assay

Get tips on using ROS-Glo™ H2O2 Assay to perform ROS assay cell type - HeLa

Products Promega ROS-Glo™ H2O2 Assay

Get tips on using EZ DNA Methylation kit to perform DNA methylation profiling Gene specific profiling - Hypothalamus mouse tissue MeCP2

Products Zymo Research EZ DNA Methylation kit

Get tips on using Cell Comb™ Scratch Assay to perform Wound healing assay cell type - mouse MS1

Products Merck Millipore Cell Comb™ Scratch Assay

Get tips on using EZ DNA Methylation-Gold Kit to perform DNA methylation profiling Gene specific profiling - HepG2 Constitutive Androstane Receptor (CAR)

Products Zymo Research EZ DNA Methylation-Gold Kit

Get tips on using MammoCult™ Human Medium Kit to perform 3D Cell Culture Media Human primary breast ephitelial cells-Mammospheres

Products STEMCELL technologies MammoCult™ Human Medium Kit

Get tips on using Acid phosphatase Assay Kit to perform Acid phosphatase assay cell type - OV2008

Products Sigma-Aldrich Acid phosphatase Assay Kit

A PCR reaction consists of the template DNA, two primers covering the amplification site, an enzyme, and buffers. A quantitative, real-time PCR reaction typically includes all of that plus a probe that can be detected fluorescently as the reaction runs, with no gel required. for detection. However, non-specific product amplification and primer-dimer formation during set-up are major causes of PCR failure. Nevertheless, high-quality DNA polymerase and optimize reaction buffers will certainly lead to a successful PCR reaction.

DNA PCR Quantitative real-time PCR Bacterial DNA

A PCR reaction consists of the template DNA, two primers covering the amplification site, an enzyme, and buffers. A quantitative, real-time PCR reaction typically includes all of that plus a probe that can be detected fluorescently as the reaction runs, with no gel required. for detection. However, non-specific product amplification and primer-dimer formation during set-up are major causes of PCR failure. Nevertheless, high-quality DNA polymerase and optimize reaction buffers will certainly lead to a successful PCR reaction.

DNA PCR Quantitative real-time PCR Mammalian DNA

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