Protein isolation Mammalian cells

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Get tips on using Minimum Essential Media (MEM) to perform Mammalian cell culture media MDCK

Products Thermo Fisher Scientific Minimum Essential Media (MEM)

Get tips on using Minimum Essential Media (MEM) to perform Mammalian cell culture media Vero

Products Thermo Fisher Scientific Minimum Essential Media (MEM)

Get tips on using Minimum Essential Medium Eagle to perform Mammalian cell culture media Vero

Products Sigma-Aldrich Minimum Essential Medium Eagle

Get tips on using Blood & Cell Culture DNA Midi Kit (25) to perform DNA isolation / purification Cells - Immortalized cell lines Human Neuroblastoma Cell Lines

Products Qiagen Blood & Cell Culture DNA Midi Kit (25)

The RNA interference (RNAi) is used to inhibit gene expression or translation, by neutralizing targeted mRNA molecules. Two types of RNA molecules such as microRNA (miRNA) and small interfering RNA (siRNA) play a central role in RNAi. Few points have to considered to increase the transfection efficiency of siRNA. Always use healthy, actively dividing cells to maximize transfection efficiency. The confluency of cells should be between 50-70%. Always use the most appropriate siRNA concentration to avoid off-target effects and unwanted toxic side effects. Positive and negative controls should be used for each and every experiment to determine transfection efficiency.

RNA siRNA / RNAi /miRNA transfection Human Cells Primary splenocytes Polymer / lipid

The RNA interference (RNAi) is used to inhibit gene expression or translation, by neutralizing targeted mRNA molecules. Two types of RNA molecules such as microRNA (miRNA) and small interfering RNA (siRNA) play a central role in RNAi. Few points have to considered to increase the transfection efficiency of siRNA. Always use healthy, actively dividing cells to maximize transfection efficiency. The confluency of cells should be between 50-70%. Always use the most appropriate siRNA concentration to avoid off-target effects and unwanted toxic side effects. Positive and negative controls should be used for each and every experiment to determine transfection efficiency.

RNA siRNA / RNAi /miRNA transfection Mouse Glomerular Mesangial cells polymer / lipid

A gross majority of classical apoptotic attributes can be quantitatively examined by flow cytometry, the preferred platform for rapid assessment of multiple cellular attributes at a single-cell level. However, sample preparation for such flow cytometry-based techniques could be challenging. Cell harvesting by trypsinization, mechanical or enzymatic cell disaggregation from tissues, extensive centrifugation steps, may all lead to preferential loss of apoptotic cells. To overcome this strictly follow manufacturers instruction of the detection kit.

Cellular assays Apoptosis assay cell type T-cells Mouse (CD4+ and CD8+)

Get tips on using Rat Endothelial Cell Growth Medium to perform Mammalian cell culture media RAOEC

Products Cell Applications Inc Rat Endothelial Cell Growth Medium

Get tips on using Porcine Endothelial Cell Growth Medium to perform Mammalian cell culture media PCAEC

Products Sigma-Aldrich Porcine Endothelial Cell Growth Medium

Get tips on using Porcine Endothelial Cell Growth Medium to perform Mammalian cell culture media PAOEC

Products Sigma-Aldrich Porcine Endothelial Cell Growth Medium

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