crispr-mouse-deletion-3t3-l1-swell1

Get tips on using BrdU antibody to perform Immunohistochemistry Mouse - BrdU

Get tips on using LC3B Antibody to perform Immunohistochemistry Mouse - LC3

Get tips on using LC3B Antibody to perform Immunohistochemistry Mouse - LC3

Get tips on using T-4103 to perform Immunohistochemistry Mouse - Somatostatin

Get tips on using T-4092 to perform Immunohistochemistry Mouse - PYY

Get tips on using Lysozyme/Muramidase to perform Immunohistochemistry Mouse - Lysozyme

The process of RNA extraction from bacteria, in general, involves an RNA-protective, effective lysis of bacterial cell wall (which may pose difficulties). EDTA promotes loss of outer membrane to provide lysozyme with access to peptidoglycan. Another common method for cell wall lysis is mechanical disruption using a homogenizer (applied for gram-positive bacteria and some strains of gram-negative bacteria). Following lysis, it is necessary to disrupt protein-nucleic acid interactions, which can be achieved by adding sodium dodecyl sulfate (SDS). Next step involves using phenol-chloroform-isoamyl alcohol extraction, where RNA can be obtained from the bottom organic phase, the top phase consists of DNA and the interphase contains proteins. Isoamyl alcohol is an inert and optional addition to this mixture and is added as an anti-foaming reagent to reduce the interphase. Following RNA extraction, the samples should be checked for its quality by gel electrophoresis (23S and 16S rRNAs and 5s rRNA and tRNA bands) or UV spectrophotometric or fluorescence methods.

Get tips on using X-AC9 to perform Immunohistochemistry Mouse - Col X

Get tips on using II-II6B3 to perform Immunohistochemistry Mouse - Col II