rna-isolation-purification-tissue-mouse-mammary-glands

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RNA Microarray Human PCOS

RNA cDNA synthesis Bacteria

Get tips on using LIVE/DEAD™ Viability/Cytotoxicity Kit, for mammalian cells to perform Live / Dead assay mammalian cells - SH-SY5Y Human neuroblastoma

Products Thermo Fisher Scientific LIVE/DEAD™ Viability/Cytotoxicity Kit, for mammalian cells

Get tips on using LIVE/DEAD™ Viability/Cytotoxicity Kit, for mammalian cells to perform Live / Dead assay mammalian cells - MCF-7 human breast cancer cells

Products Thermo Fisher Scientific LIVE/DEAD™ Viability/Cytotoxicity Kit, for mammalian cells

Get tips on using QuantiNova Probe PCR Kit (2500) to perform PCR Quantitative real-time PCR - Mammalian DNA

Products Qiagen QuantiNova Probe PCR Kit (2500)

Get tips on using LIVE/DEAD™ Viability/Cytotoxicity Kit, for mammalian cells to perform Live / Dead assay mammalian cells - MDA-MB-231 human breast cancer cells

Products Thermo Fisher Scientific LIVE/DEAD™ Viability/Cytotoxicity Kit, for mammalian cells

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. When using oligos, the ideal concentration lies between 10-50nM for effective transfection.

RNA siRNA / miRNA gene silencing Human MCF-7 PRC (PGC-1α–related coactivator)/PPRC1

Get tips on using QuantiTect SYBR Green PCR Kit (1000) to perform PCR Quantitative real-time PCR - Mammalian DNA

Products Qiagen QuantiTect SYBR Green PCR Kit (1000)

Get tips on using miScript SYBR Green PCR Kit (2000) to perform PCR Quantitative real-time PCR - Mammalian DNA

Products Qiagen miScript SYBR Green PCR Kit (2000)

Get tips on using SYBR™ Green PCR Master Mix to perform PCR Quantitative real-time PCR - Mammalian DNA

Products Thermo Fisher Scientific SYBR™ Green PCR Master Mix

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