초록 ▼

pK-matched buffers, each containing two effective buffering components: one weak base and one weak acid which have similar pKa at 25째 C. (within 0.3 pK units). On agarose gels, the buffers in various concentrations were tested for separation of double-stranded DNA fragments with various DNA markers,

pK-matched buffers, each containing two effective buffering components: one weak base and one weak acid which have similar pKa at 25째 C. (within 0.3 pK units). On agarose gels, the buffers in various concentrations were tested for separation of double-stranded DNA fragments with various DNA markers, agarose gel concentrations, and field strengths. Mobility was inversely proportional to the logarithm of molecular weight. The buffers provided high resolution without smearing at more dilute concentration than is possible with standard TAE (Tris/Acetate, pH 8.0) or TBE (Tris/Borate, pH 8.3) buffers. The buffers were also tested in 7M urea denaturing LongRanger짰 sequencing gels and in non-denaturing polyacrylamide SSCP gels. The pK-matched buffers provide good separation and high resolution, at a broad range of potential pH values. In comparison to TAE and TBE, pK-matched buffers provide higher voltage and current stability, lower working concentration, more concentrated stock solutions, and lower current per unit voltage, resulting in less heat generation.

대표청구항 ▼

The invention claimed is: 1. In an electrophoresis method, the improvement which comprises running the electrophoresis in a pK-matched buffer selected from the group consisting of a buffer comprising CAPSO and ethanolamine; a buffer comprising ACES and BIS-TRIS; a buffer comprising CAPSO and 2-amin

The invention claimed is: 1. In an electrophoresis method, the improvement which comprises running the electrophoresis in a pK-matched buffer selected from the group consisting of a buffer comprising CAPSO and ethanolamine; a buffer comprising ACES and BIS-TRIS; a buffer comprising CAPSO and 2-amino-2-methyl-1-propanol; and a buffer comprising HEPES and triethanolamine. 2. The improvement of claim 1, wherein the method is a gel electrophoresis method for separating nucleic acids or polypeptides. 3. The improvement of claim 1, wherein the pk-matched buffer is a buffer comprising CAPSO and ethanolamine. 4. The improvement of claim 1, wherein the pK-matched buffer is a buffer comprising ACES and BIS-TRIS. 5. The improvement of claim 1, wherein the pK-matched buffer is a buffer comprising CAPSO and 2-amino-2methyl-1-propanol. 6. The improvement of claim 1, wherein the pK-matched buffer is a buffer comprising HEPES and triethanolamine.