Cell Isolation

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Get tips on using Cell Counting Kit-8 to perform Cell cytotoxicity / Proliferation assay cell type - MCF-7

Products Dojindo Cell Counting Kit-8

Get tips on using BrdU Cell Proliferation Assay to perform Cell cytotoxicity / Proliferation assay cell type - SKOV-3

Products Millipore BrdU Cell Proliferation Assay

Get tips on using Cell Counting Kit-8 to perform Cell cytotoxicity / Proliferation assay cell type - OVCAR-3

Products Dojindo Cell Counting Kit-8

Get tips on using Cell Counting Kit-8 to perform Cell cytotoxicity / Proliferation assay cell type - DU-145

Products Dojindo Cell Counting Kit-8

Get tips on using Cell Counting Kit-8 to perform Cell cytotoxicity / Proliferation assay cell type - PC-3

Products Dojindo Cell Counting Kit-8

Get tips on using Cell Counting Kit-8 to perform Cell cytotoxicity / Proliferation assay cell type - Hep G2

Products Dojindo Cell Counting Kit-8

Get tips on using Cell Proliferation ELISA, BrdU to perform Cell cytotoxicity / Proliferation assay cell type - Hep G2

Products Sigma-Aldrich Cell Proliferation ELISA, BrdU

Get tips on using Cell Proliferation ELISA, BrdU to perform Cell cytotoxicity / Proliferation assay cell type - 3T3-L1

Products Sigma-Aldrich Cell Proliferation ELISA, BrdU

Transfection is a powerful technique that enables the study of the function of genes and gene products in cells. Based on the nature of experiments, we may need a stable DNA transfection in cells for persistent gain-of-function or loss-of-function of the target gene. For stable transfection, integration of a DNA vector into the chromosome is crucial which requires selective screening and clonal isolation. By carefully selecting a viral delivery system and related reagents we can ensure safe and highly-efficient delivery of expression constructs for high-level constitutive or inducible expression in any mammalian cell type.

DNA DNA transfection Mammalian cells Primary cells Rat pulmonary artery smooth muscle cell (pPASMC)

Contamination can affect cell characteristics, i.e., growth, metabolism, and morphology leading to unreliable and erroneous experimental data. Depending on the source of contaminants, one can detect contamination by using a light microscope, gram stain, isothermal amplification, or PCR. Bacteria and fungi can usually be identified by optical microscopy. Mycoplasma in cell cultures cannot be detected visually. Hence, these microbes can go unnoticed for long periods and are determined using dedicated assays. Early and rapid identification of contaminants is vital to detect, handle and prevent contamination for good cell-culture practices. However, detection and identification can be challenging and tricky based on usual visual identifications. Hence it is essential to use a standard contamination detection kit to detect and maintain best practices.

Cellular assays Cell Culture Contamination Detection Kit Mycoplasma

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