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The electrophoresis buffers maintain consistent pH levels during DNA, RNA, and other protein separation. Providing ions that transfer the applied current, the low charge solutions facilitate different molecular sizes to travel at various rates for analyses. Offering additional protection to proteins, the preparative substances prevent degradation for guaranteed sample viability and accurate testing. Available in various molecular weights, the best electrophoresis buffer can be selected based on the specific macromolecules being handled.
Description:
IPG Buffer pH 6-11, 1 ml. For use with Immobiline DryStrip gels to improve protein solubility.Ensures optimal conditions for IEF separation.Eliminates background staining. Category: Proteomics, Expression Analysis, 2-D Electrophoresis.
Description:
SSC 20X 500ml; NaCl 175.32 g/L 3M; sodium citrate 2H2O 88.23 g/L 0.3M; sufficient HCl to adjust to pH 7.0. This stock solution can be used to prepare DNA and RNA transfer buffer, DNA and RNA hybridization buffers, and post-hybridization membrane washing buffers.
Description:
TAE (Tris-Acetate EDTA), 10X, Recipe: 48.46g TRIS Base, 11.4ml Acetic Acid, 3.72g EDTA, Sterile Filtered: (0.20 uM), Polycarbonate Bottle, Storage: Room Temperature, used in agarose gel electrophoresis & Polyacrylamide gels both as a buffer & a component of a gel, Size: 2L
Description:
For use in ELISA. Designed to stabilize antigens. After the addition of blocking agent, wash the contents of the ELISA microwell and add a sufficient volume of ELISA Microwell Coating Stabilizer to each well of the microplate.