siRNA / miRNA gene silencing Human MDA-MB-231

Get tips on using Autophagy Inhibitor, 3-MA to perform Autophagy assay cell type - U251MG

Get tips on using Autophagy Inhibitor, 3-MA to perform Autophagy assay cell type - U87MG

Get tips on using Autophagy Inhibitor, 3-MA to perform Autophagy assay cell type - U87MG

Get tips on using Atg5 (D5F5U) Rabbit mAb to perform Autophagy assay cell type - A549

Get tips on using Promega PCR Master Mix to perform PCR Multiplex PCR - Bacterial DNA

Get tips on using Mastermix 16S Complete to perform PCR Quantitative real-time PCR - Bacterial DNA

Get tips on using Atg7 (D12B11) Rabbit mAb to perform Autophagy assay cell type - HeLa

A gross majority of classical apoptotic attributes can be quantitatively examined by flow cytometry, the preferred platform for rapid assessment of multiple cellular attributes at a single-cell level. However, sample preparation for such flow cytometry-based techniques could be challenging. Cell harvesting by trypsinization, mechanical or enzymatic cell disaggregation from tissues, extensive centrifugation steps, may all lead to preferential loss of apoptotic cells. To overcome this strictly follow manufacturers instruction of the detection kit.

A gross majority of classical apoptotic attributes can be quantitatively examined by flow cytometry, the preferred platform for rapid assessment of multiple cellular attributes at a single-cell level. However, sample preparation for such flow cytometry-based techniques could be challenging. Cell harvesting by trypsinization, mechanical or enzymatic cell disaggregation from tissues, extensive centrifugation steps, may all lead to preferential loss of apoptotic cells. To overcome this strictly follow manufacturers instruction of the detection kit.

A gross majority of classical apoptotic attributes can be quantitatively examined by flow cytometry, the preferred platform for rapid assessment of multiple cellular attributes at a single-cell level. However, sample preparation for such flow cytometry-based techniques could be challenging. Cell harvesting by trypsinization, mechanical or enzymatic cell disaggregation from tissues, extensive centrifugation steps, may all lead to preferential loss of apoptotic cells. To overcome this strictly follow manufacturers instruction of the detection kit.