dna-methylation-profiling-gene-specific-profiling-caco-1-chst11

Get tips on using 3-Methyladenine (3-MA) to perform Autophagy assay cell type - HL-1

Get tips on using FITC BrdU Flow Kit to perform Cell cycle assay human - THP-1

Get tips on using Atg12 (D88H11) Rabbit mAb to perform Autophagy assay cell type - THP 1

Get tips on using Atg7 (D12B11) Rabbit mAb to perform Autophagy assay cell type - THP 1

Get tips on using Atg5 (D5F5U) Rabbit mAb to perform Autophagy assay cell type - THP 1

Get tips on using Mouse SDF1 ELISA Kit (ab100741) to perform ELISA Mouse - SDF-1/CXCL12

Get tips on using Recombinant Anti-MUC1 antibody [EPR1023] (ab109185) to perform Immunohistochemistry Human - Muc-1

Get tips on using ChIP Kit Magnetic - One Step (ab156907) to perform ChIP Human - PANC-1

Get tips on using TACS Annexin V-FITC Apoptosis Detection Kit to perform Necrosis PANC-1

Plasmid isolation is an important technique in molecular biology or any kind of genetic editing. It involves amplifying plasmids overnight by transforming them into competent bacterial cells. The desired colonies of these bacteria can then be grown in shaker cultures, at appropriate shaking speed, oxygen availability and temperature. These liquid cultures can then be ultracentrifuged to pellet the bacteria, which are then used for plasmid isolation. The bacteria are first resuspended in a buffer, then lysed, neutralized, purified in a column, eluted, precipitated with ethanol and then resuspended. During plasmid isolation, it is important to lyse cells quickly because lysing bacteria for too long may lead to irreversible denaturing of the plasmid. Usually, alkaline lysis is used for isolation because it is a mild treatment. It isolates plasmid DNA and other cell components such as proteins by breaking cells apart with an alkaline solution. Precipitation removes the proteins, and the plasmid DNA recovers with alcohol precipitation. Resuspension and lysis buffers should be mixed thoroughly in order to prevent the DNA from breaking into smaller fragments. This is because broken gDNA can reanneal and remain in the solution, without binding to the column.