CRISPR Mouse Deletion RAW 264.7

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Get tips on using VENTANA anti-MLH1 (M1) Mouse Monoclonal Primary Antibody to perform Immunohistochemistry Human - MLH1

Products Roche Lifesciences VENTANA anti-MLH1 (M1) Mouse Monoclonal Primary Antibody

Get tips on using Monoclonal Anti-Connexin-43 antibody produced in mouse to perform Western blotting CX43

Products Sigma-Aldrich Monoclonal Anti-Connexin-43 antibody produced in mouse

Get tips on using SurePrint G3 Mouse Exon 4x180K Microarray Kit (165,984 Exon probes) to perform Microarray Gene expression arrays - Mouse Cyanine-CTP

Products Agilent Technologies SurePrint G3 Mouse Exon 4x180K Microarray Kit (165,984 Exon probes)

RNA RNA isolation / purification Tissue Mouse Vagina

Get tips on using CD273 (PD-L2) Antibody, anti-mouse, PerCP-Vio® 700 to perform Flow cytometry Anti-bodies Mouse - CD273/PD-L2

Products Miltenyibiotec CD273 (PD-L2) Antibody, anti-mouse, PerCP-Vio® 700

Get tips on using Monoclonal Anti-γ-Tubulin antibody produced in mouse to perform Western blotting tubulin gamma

Products Sigma-Aldrich Monoclonal Anti-γ-Tubulin antibody produced in mouse

Get tips on using Monoclonal Anti-Caveolin-1 antibody produced in mouse to perform Western blotting Caveolin-1

Products Sigma-Aldrich Monoclonal Anti-Caveolin-1 antibody produced in mouse

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 mouse splenocytes

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 mouse cardiomyocytes

Isolating RNA from tissues and paraffin-embedded tissue samples can be challenging due to cross-linking of biomolecules and fragmented nucleic acids. The best solution is to slice the tissues into smaller pieces and make a homogenate solution (using tissue homogenizer or grinding liquid nitrogen frozen samples) in presence of RNAse inhibitors. The homogenization process should be carried out on dry ice to maintain the integrity of RNA.

RNA RNA isolation / purification Tissue Mouse Adipose

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