RNA isolation / purification Cells immortalized

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Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - PANC-1

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - AsPC-1

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - SKBR-3

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - MCF-7

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - SH-SY5Y

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using Ni-NTA Agarose to perform Protein expression and purification Insect cells - Hi5 TYR

Products Qiagen Ni-NTA Agarose

Short hairpin or small hairpin RNA (shRNA) is artificial RNA, which has a hairpin loop structure, and uses inherent microRNA (miRNA) machinery to silence target gene expression. This is called RNA interference (RNAi). These can be delivered via plasmids or viral/bacterial vectors. Challenges in shRNA-mediated gene silencing include 1. Off-target silencing, 2. Packaging shRNA encoding lentivirus, and 3. Stable transduction in cells. RNAi has been designed to have anywhere from 19-27 bs, but the most effective design has 19 bp. In case commercial shRNAs are not available, potential target sites can be chosen within exon, 5’- or 3’ UTR, depending on which splice variants of the gene are desired. One should use the latest algorithms and choose at least two different sequences, targeting different regions, in order to have confidence in overcoming off-target effects. A BLAST search after selecting potential design will eliminate potential off-target sequences. For the second challenge, sequencing the vector using primers for either strand (50-100 bp upstream) is suggested, along with using enzymatic digestion on agarose gel for the vector. Next, once the shRNA-containing vector is packaged in a virus, it is important to check the viral titer before transduction. Finally, using a marker in the lentiviral vector (fluorescent protein or antibiotic resistance), along with qPCR for target gene expression can help in determining the efficacy of transduction and shRNA on its target site.

RNA shRNA gene silencing Human Neuroblastoma cells (SH-SY5Y) Beclin 1

Get tips on using TRI Reagent® to perform Protein isolation Mammalian cells - Mouse_Brown fat

Products Sigma-Aldrich TRI Reagent®

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - MIA PaCa-2

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Human - iPSC-derived cardiomyocytes

Products Illumina TruSeq RNA Library Prep Kit v2

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