Buffers & Concentrates

Tris-Acetate-EDTA (TAE) is a buffer solution containing a mixture of Tris base, acetic acid and EDTA. TAE suitable for multiple molecular biology applications including agarose electrophoresis for the separation of nucleic acids such as DNA and RNA.

Tris-Acetate-EDTA (TAE) is a buffer solution containing a mixture of Tris base, acetic acid and EDTA. TAE suitable for multiple molecular biology applications including agarose electrophoresis for the separation of nucleic acids such as DNA and RNA.

Tris-Phosphate-EDTA (TPE) is a commonly used buffer solution in molecular biology, especially for gel electrophoresis and gene expression studies. The purpose of TPE buffer is to solubilize DNA or RNA, while protecting it from degradation.

Destain Solution is a uniquely formulated, ready-to-use reagent specifically designed for destaining Coomassie Blue stained polyacrylamide gels.

Western Blotting is the method used for immunodetection for the detection of proteins. Blotting is a method for transferring biological molecules (e.g., proteins, nucleic acid fragments) from a gel matrix to a membrane support for the subsequent detection of those molecules.

Tris solution is an abbreviation of the organic compound known as tris(hydroxymethyl)aminomethane. Tris is extensively used in biochemistry and molecular biology. In biochemistry, Tris is widely used as a component of additional buffer solutions, such as in TAE and TBE buffer, especially for solutions of nucleic acids. Visit our newly expanded web site at www.rockland.com for methods using this and other buffers.

Tris solution is an abbreviation of the organic compound known as tris(hydroxymethyl)aminomethane. Tris is extensively used in biochemistry and molecular biology. In biochemistry, Tris is widely used as a component of buffer solutions, such as in TAE and TBE buffer, especially for solutions of nucleic acids.

Tris-Glycine Running Gel buffer without SDS (sodium dodecyl sulfate) for polyacrylamide gel electrophoresis, describes a technique widely used in biochemistry to separate proteins according to their electrophoretic mobility (a function of the length of a polypeptide chain and its charge) and no other physical feature. SDS is an anionic detergent applied to protein sample to linearize proteins and to impart a negative charge to linearized proteins.

Tris-Glycine Running Gel buffer without SDS (sodium dodecyl sulfate) for polyacrylamide gel electrophoresis, describes a technique widely used in biochemistry to separate proteins according to their electrophoretic mobility (a function of the length of a polypeptide chain and its charge) and no other physical feature. SDS is an anionic detergent applied to protein sample to linearize proteins and to impart a negative charge to linearized proteins.