All bioWORLD running buffers are prepared with high quality reagents.

Tris-Tricine (TT) Buffer has been developed for both non-denaturing and denaturing electrophoresis of proteins, and offers several advantages over more conventionally used buffers. TT Buffer allows for optimal resolution of low molecular weight proteins and elimantes the glycine front often found…

Acrylamide and bis-acrylamide are major ingredients in polyacrylamide gels, a commonly used matrix for electrophoretic separation of nucleic acids and proteins. Fragments of DNA produced by various molecular biology techniques (eg. restriction endonuclease digestion, dideoxy sequencing, or the…

1X concentration contains: 50mM Tris-HCl (pH 6.8) 2% SDS 10% Glycerol 1% β Mercaptoethanol 12.5mM EDTA 0.02% Bromophenol Blue

NFDM Diluent/Blocking 10X, in a priority physiological saline borate buffer is used to minimize non-specific binding of antibody. Technical Information: pH 7.6 Sold as 10 x 100mL.

Blot blocking buffer used to block non-specific binding site for antibodies on the membrane. Technical Information: 10% Horse serum, 0.02% sodium azide in PBS

These convenient 50 mM premixed and ready-to-use A.C.E.™ Phosphate Buffers have been specially formulated for Capillary Electrophoresis. They are ideal for the separation of various biomolecules including proteins. Manufactured with the highest quality reagents in nucleasefree water, AMRESCO…

Sample buffer for protein analysis. 2X Concentration Contains: 450mM Tris-HCl, pH 8.45, 4% SDS, 10% Glycerol, 0.0025% Coomassie blue G, 2% β-Mercaptoethanol.

Sample buffer for protein analysis. 2X Concentration Contains: Tris-HCl, pH 8.45 (900mM), SDS (8%), Glycerol (20%), Coomassie blue G (0.01%).

Proteomics Grade An electrophoresis running buffer for DNA Sequencing that yields longer reads

Sample buffer for protein analysis.

Western Blot Buffer Proteomics Grade

bioWORLD running buffers are prepared with high quality reagents.

2-Iminothiolane Primary amine reactive Introduces sulhydryls Water soluble

Product contains enough liquid concentrate to make 1L of 1X solution. To use this product, dilute it 4 fold with DI water and add 0.6% beta ME. Wash membrane in this buffer and incubate at 65°C for 30 minutes under constant agitation. Wash the membrane 5X for 5 min in PBS-Tween20 or…