Protein expression and purification Insect cells

Get tips on using Absolutely Total RNA Purification Kits to perform RNA isolation / purification Cells - primary rat cardiac fibroblasts

Get tips on using DC™ Protein Assay Kit I to perform Protein quantification Tissue - mouse liver

Get tips on using DC™ Protein Assay Kit I to perform Protein quantification Tissue - mouse kidney

Get tips on using DC™ Protein Assay Kit I to perform Protein quantification Tissue - mouse brain

Get tips on using DC™ Protein Assay Kit I to perform Protein quantification Tissue - mouse thymus

Get tips on using DC™ Protein Assay Kit I to perform Protein quantification Tissue - mouse spleen

Get tips on using DC™ Protein Assay Kit I to perform Protein quantification Tissue - mouse aorta

Isolating DNA from tissues and paraffin-embedded tissue samples can be challenging as double-stranded DNA is physically fragile and highly susceptible to exo- and endonucleases. 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 the presence of DNAse inhibitors. Further, extracting DNA from the nucleus need specific methods by combining physical, mechanical and chemical lysis approaches,

Reporter gene assays enable high sensitivity measurement of gene expression and cell signaling through the addition of bioluminescent genes into target cells. One of the major challenges is to make a specific construct that has no responses other than those related to the signaling pathway of interest. This can be achieved by selecting highly specific reporter constructs containing only defined responsive elements and a minimal promoter linked to reporter enzymes such as luciferase

Reporter gene assays enable high sensitivity measurement of gene expression and cell signaling through the addition of bioluminescent genes into target cells. One of the major challenges is to make a specific construct that has no responses other than those related to the signaling pathway of interest. This can be achieved by selecting highly specific reporter constructs containing only defined responsive elements and a minimal promoter linked to reporter enzymes such as luciferase