ChIP H3K9Ac Mouse

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Get tips on using Anti-trimethyl-Histone H3 (Lys27) Antibody to perform ChIP Anti-bodies H3K27me3

Products Millipore Anti-trimethyl-Histone H3 (Lys27) Antibody

Get tips on using Anti-dimethyl-Histone H3 (Lys27) Antibody to perform ChIP Anti-bodies H3K27me2

Products Merck Millipore Anti-dimethyl-Histone H3 (Lys27) Antibody

Get tips on using Anti-monomethyl-Histone H3 (Lys27) Antibody to perform ChIP Anti-bodies H3K27me1

Products Merck Millipore Anti-monomethyl-Histone H3 (Lys27) Antibody

Get tips on using Anti-dimethyl-Histone H3 (Lys4) Antibody to perform ChIP Anti-bodies H3K4me2

Products Merck Millipore Anti-dimethyl-Histone H3 (Lys4) Antibody

Get tips on using Anti-monomethyl-Histone H3 (Lys4) Antibody to perform ChIP Anti-bodies H3K4me1

Products Merck Millipore Anti-monomethyl-Histone H3 (Lys4) Antibody

Get tips on using TFIIB Antibody (D-3): sc-271736 to perform ChIP Anti-bodies TFIIB

Products Santa Cruz Biotechnology TFIIB Antibody (D-3): sc-271736

Get tips on using STAT5 beta Monoclonal Antibody (ST5b-10G1) to perform ChIP Anti-bodies Stat5b

Products Thermo Fisher Scientific STAT5 beta Monoclonal Antibody (ST5b-10G1)

Get tips on using Stat5b Antibody (C-8): sc-377069 to perform ChIP Anti-bodies Stat5b

Products Santa Cruz Biotechnology Stat5b Antibody (C-8): sc-377069

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 have 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 efficacy of transduction and shRNA on its target site.

RNA shRNA gene silencing Mouse Prostate cancer cell lines (DU145 and PC3) CD24 lentiviral particles

Get tips on using Anti-acetyl-Histone H4 Antibody to perform ChIP acH4 - Rabbit Sheep YFP Tag

Products Millipore Anti-acetyl-Histone H4 Antibody

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