In-gel fluorescent stain for proteins, providing excellent sensitivity (10ng) more quickly than any other detection method. The Insite stain runs with the proteins during electrophoresis. No staining step is required after electrophoresis. To use...
Insite Markers contain both visible markers for orientation during the run and high precision protein standards (10 - 225 kD) that appear with fluorescent detection. This allows both confident monitoring of the run and precise assignment of protein...
Mixture of anionic and cationic resins specially prepared for the deionization of electrophoretic gel monomer solutions prior to initiation.
Used to cleave disulfide linkages prior to protein electrophoresis. Triple distilled to remove impurities and stored under nitrogen.
Popular buffer formula for SDS-PAGE of proteins. 20X concentrate makes a buffer containing 50mM Tris-MES, 0.1% SDS and 1mM EDTA.
Ideal running buffer for high resolution SDS PAGE of proteins. 20X concentrate makes a working solution of 50mM Tris MOPS, 0.1% SDS and 1mM EDTA.
Ready-to-use sodium chloride-tris buffer solution. It is especially designed for use in Southern and Northern Blotting, and in situ hybridization procedures. Neutralization Solution contains 3M NaCl and 0.5M Tris in distilled/deionized .
Nuclistain is intended as a replacement for the conventionally used ethidium bromide for the rapid detection of double and single stranded DNA and RNA in agarose and polyacrylamide gels. Its sensitivity is nearly comparable, with the capability of...
Nuclistain is intended as a replacement for the conventionally used ethidium bromide for the rapid detection of double and single stranded DNA and RNA in agarose and polyacrylamide gels. Its sensitivity is nearly comparable, with the capability of...