Stem cell Differentiation media

Get tips on using Cytotoxicity Detection KitPLUS (LDH) to perform Cell cytotoxicity / Proliferation assay cell type - HT-22

Get tips on using LDH Cytotoxicity Detection Kit to perform Cell cytotoxicity / Proliferation assay cell type - 3T3-L1

Get tips on using PowerPlex® Fusion 6C System to perform Cell line authentication ML14 lymphoblastoid cell line

Get tips on using PowerPlex® 16 HS System to perform Cell line authentication Glioblastoma cell line U138MG

Get tips on using PowerPlex® 16 HS System to perform Cell line authentication Glioblastoma cell line HS683

Get tips on using 48-Well Micro Chemotaxis Chamber to perform Cell migration / Invasion cell type - HT-1080

Get tips on using Beclin-1 (D40C5) Rabbit mAb to perform Cell cytotoxicity / Proliferation assay cell type - K562

Get tips on using CYTO-ID® Autophagy detection kit to perform Autophagy assay cell type - Fibroblast cell

Get tips on using EasySep™ Release Human CD19 Positive Selection Kit to perform Cell Isolation B cell

RNAi or RNA interference is a common method to suppress gene expression in vitro/in vivo by utilizing the inherent microRNA machinery, without introducing a total gene knockout. miRNA is the inherent gene silencing machinery which can have more than one mRNA target, whereas siRNA can be designed to target a particular mRNA target. By design, both siRNA and miRNA are 20-25 nucleotides in length. The target sequence for siRNAs is usually located within the open reading frame, between 50 and 100 nucleotides downstream of the start codon. There are two ways in which cells can be transfected with desired RNAi: 1. Direct transfection (with calcium phosphate co-precipitation or cationic lipid-mediated transfection using lipofectamine or oligofectamine), and 2. Making RNAi lentiviral constructs (followed by transformation and transduction). Lentiviral constructs are time-consuming, but provide a more permanent expression of RNAi in the cells and consistent gene silencing. Direct transfection of oligonucleotides provides temporary genetic suppression. Traditional methods like calcium phosphate co-precipitation have challenges like low efficiency, poor reproducibility and cell toxicity. Whereas, cationic lipid-based transfection reagents are able to overcome these challenges, along with applicability to a large variety of eukaryotic cell lines.