siRNA / RNAi /miRNA transfection Human Cells HeLa

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Cells are sourced from various tissues to grow them in in-vitro conditions. Therefore, cell specific nutrients are important for their survival, maintenance and growth. Determining the appropriate cell culture media is a challenge if you are growing a cell line or a microorganism for the first time. Established cell lines, primary cells, stem cells, bacteria and Yeast all require varied nutrients from basic to complex. Based on the cell type, one can easy find what media and nutrients your peers have used before you try to reinvent the wheel.

Cell culture media Mammalian cell culture media HSG cells
ISOGEN Product

Get tips on using ISOGEN to perform RNA isolation / purification Cells - primary human epidermal melanocytes

Products Nippon Gene ISOGEN

Get tips on using TRIzol Reagent to perform RNA isolation / purification Cells - primary human preadipocytes

Products Thermo Fisher Scientific TRIzol Reagent

Get tips on using TRIzol Reagent to perform RNA isolation / purification Cells - primary human chondrocytes

Products Thermo Fisher Scientific TRIzol Reagent

ROS has a very short half-lives in biological environment as they are influenced by exposure to ambient oxygen. As it is highly reactive and hard to measure care should be taken to ensure the stability of the sample during isolation, preparation, storage, and analysis.

Cellular assays ROS assay cell type PLHC-1, SK-HEP-1, Hep3b, HepG2 human hepatocellular carcinoma

The estimation of DNA methylation level heavily depends on the complete conversion of non-methylated DNA cytosines. It is crucial to ensure complete conversion of non-methylated cytosines in DNA. Therefore, it is important to incorporate controls for bisulfite reactions, as well as to pay attention to the appearance of cytosines in non-CpG sites after sequencing, which is an indicator of incomplete conversion.

DNA DNA methylation profiling Whole genome profiling DU145, PC3 human prostate cancer

The estimation of DNA methylation level heavily depends on the complete conversion of non-methylated DNA cytosines. It is crucial to ensure complete conversion of non-methylated cytosines in DNA. Therefore, it is important to incorporate controls for bisulfite reactions, as well as to pay attention to the appearance of cytosines in non-CpG sites after sequencing, which is an indicator of incomplete conversion.

DNA DNA methylation profiling Whole genome profiling OVCAR-3 human ovarian cancer

Get tips on using Monoclonal Mouse Anti-Human Actin (Smooth Muscle) (Concentrate) Clone 1A4 to perform Immunohistochemistry Mouse - SMA

Products Agilent Technologies Monoclonal Mouse Anti-Human Actin (Smooth Muscle) (Concentrate) Clone 1A4

Get tips on using Human/Mouse GFR alpha-2/GDNF R alpha-2 Antibody to perform Immunohistochemistry Mouse - Gfrα2

Products R&D system, Minneapolis, MN, USA Human/Mouse GFR alpha-2/GDNF R alpha-2 Antibody

Cellular assays Cell Isolation hematopoietic stem cells

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