Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - Goblet cells
Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - PANC-1
Get tips on using LC3B (D11) XP® Rabbit mAb to perform Autophagy assay cell type - SAE cells
Get tips on using LC3B (D11) XP® Rabbit mAb to perform Autophagy assay cell type - PC-12
Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - THP 1
Get tips on using LC3B (D11) XP® Rabbit mAb to perform Autophagy assay cell type - SH-SY5Y
Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - SH-SY5Y
Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - MCF-7
Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - K562 cells
Western blotting is a widely used technique to size separate proteins from a pool of cell or tissue lysates. The technique has 4 major steps: a) gel electrophoresis, b) blocking and treatment with antigen specific antibody, c) treatment with secondary antibody and finally d) detection and visualization. Though western blotting is a widely used technique, detection of specific proteins depends on several factors, the major ones are antibody concentration, incubation time and washing steps. Key points for obtaining clean blots are: always prepare fresh buffer solutions and optimize antibody concentration. Given the advent of high-throughput protein analysis and a push to limit the use of lab consumables, onestep antibodies are developed which recognise protein of interest and also contain a detection label.
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