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A Guide to Biological Buffer Preparation for pH Measurement and Pipetting

A Guide to Biological Buffer Preparation for pH Measurement and Pipetting

15 Sept 2015

Researchers in Life Sciences carry out work on biological molecules, such as antibodies or proteins, in order to modify them for their purposes, often in the search for disease cures and prevention. Almost all biological processes are pH dependent. The purpose of buffer in a biological system is to maintain intracellular and extracellular pH within a very narrow range and resist changes in pH in the presence of internal and external influences. The rather complex laboratory buffer preparation process involves a number of different steps, including amount calculation, substance weighing, pH solution value control and liquid pipetting. This application note explains some useful tips and hints for the use of pipettes and pH Meters in the preparation of buffers.

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Sample PreparationSample preparation can improve the quality and speed of separation techniques. Products to assist sample preparation include filtration equipment, evaporators, membranes and sieves.AntibodiesAntibodies are used in techniques such as confocal and fluorescence microscopy, flow cytometry, ELISA, ELISPOT, immunohistochemistry, western blotting and immunopreciptation. Select specific antigen reactivity, high specific affinity, low non-specific binding, monoclonal or polyclonal, primary or secondary antibodies and associated conjugates such as an enzyme or dye for visualization.Antibody PurificationProtein BiologyThe analysis of protein expression, identity and function is vital for many areas of life science research and drug discovery. Some of the most commonly used techniques in protein analysis include Western blotting, electrophoresis and mass spectrometry.
A Guide to Biological Buffer Preparation for pH Measurement and Pipetting