siRNA / miRNA gene silencing Human PC3 (human prostate cancer cell line)

- Found 9155 results

Get tips on using MISSION® esiRNA_esiRNA targeting mouse Lrp6 (esiRNA1) to perform siRNA / miRNA gene silencing Mouse - MLO‐Y4 Lrp6

Products Sigma-Aldrich MISSION® esiRNA_esiRNA targeting mouse Lrp6 (esiRNA1)

Get tips on using AmpFLSTR™ Identifiler™ Direct PCR Amplification Kit to perform Cell line authentication Human iPSC cells derived from human dermal fibroblasts

Products Thermo Fisher Scientific AmpFLSTR™ Identifiler™ Direct PCR Amplification Kit

Cell culture media 3D Cell Culture Media Human esophageal organoids

Cell culture media 3D Cell Culture Media Human pancreatic organoids

Cell culture media 3D Cell Culture Media Human endometrium organoids

Cell culture media 3D Cell Culture Media Human gastric organoids

ROS has a very short half-lives in biological environment as they are influenced by exposure to ambient oxygen. As it is highly reactive and hard to measure care should be taken to ensure the stability of the sample during isolation, preparation, storage, and analysis.

Cellular assays ROS assay cell type K562 human leukemia cells

RNA siRNA / RNAi /miRNA transfection Bovine monocyte-derived macrophages

As autophagy is a multi-step process which includes not just the formation of autophagosomes, but most importantly, flux through the entire system, including the degradation upon fusion with lysosomes, which makes it quite challenging for detection. There are several methods for detection in mammalian cells, including immunoblotting analysis of LC3 and p62 and detection of autophagosome formation/maturation by fluorescence microscopy, Currently, there is no single “gold standard” for determining the autophagic activity that is applicable in every experimental context, hence it is recommended to go for the combined use of multiple methods to accurately assess the autophagic activity in any given biological setting.

Cellular assays Autophagy assay cell type Human primary MSCs

As autophagy is a multi-step process which includes not just the formation of autophagosomes, but most importantly, flux through the entire system, including the degradation upon fusion with lysosomes, which makes it quite challenging for detection. There are several methods for detection in mammalian cells, including immunoblotting analysis of LC3 and p62 and detection of autophagosome formation/maturation by fluorescence microscopy, Currently, there is no single “gold standard” for determining the autophagic activity that is applicable in every experimental context, hence it is recommended to go for the combined use of multiple methods to accurately assess the autophagic activity in any given biological setting.

Cellular assays Autophagy assay cell type Human Tenon fibroblasts

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