三羟甲基氨基甲烷醋酸盐
三羟甲基氨基甲烷醋酸盐结构式
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常用名 | 三羟甲基氨基甲烷醋酸盐 | 英文名 | Tris acetate |
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| CAS号 | 6850-28-8 | 分子量 | 181.187 | |
| 密度 | 1.09 g/mL at 20 °C | 沸点 | 219-220 °C (9.7513 mmHg) | |
| 分子式 | C6H15NO5 | 熔点 | 120-121 °C | |
| MSDS | 美版 | 闪点 | 169.7ºC |
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Displaceable binding of [3H]l-glutamic acid to non-receptor materials.
Life Sci. 38 , 1089, (1986) [3H]L-glutamic acid binding to microfuge tubes and glass was investigated in four buffers. Background binding to these materials was negligible, but was increased by centrifugation or suction in Tris-HCl and Tris-citrate buffer. This binding was much less or ... |
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Choice of buffer anion for the assay of adenosine 5'-triphosphate using firefly luciferase.
Anal. Biochem. 114 , 396, (1981)
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Peroxidase mimicking DNA-gold nanoparticles for fluorescence detection of the lead ions in blood.
Analyst 137 , 5222-5228, (2012) Oligonucleotide (T30695) modified gold nanoparticles (T30695-Au NPs) have been prepared and employed for quantification of lead ions (Pb(2+)) in blood. The detection of Pb(2+) ions is through the formation of Au-Pb alloys and oligonucleotide-Pb(2+) complexes ... |
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Tris-acetate polyacrylamide gradient gels for the simultaneous electrophoretic analysis of proteins of very high and low molecular mass.
Methods Mol. Biol. 869 , 205-213, (2012) Polyacrylamide gel electrophoresis (PAGE) is one of the most powerful tools used for protein analysis. We describe the use of Tris-acetate buffer and 3-15% polyacrylamide gradient gels to simultaneously separate proteins in the mass range of 10-500 kDa. We sh... |
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Simultaneous electrophoretic analysis of proteins of very high and low molecular mass using Tris-acetate polyacrylamide gels.
Electrophoresis 31 , 1318-1321, (2010) To separate and analyze giant and small proteins in the same electrophoresis gel, we have used a 3-15% polyacrylamide gradient gel containing 2.6% of the crosslinker bisacrylamide and 0.2 M of Tris-acetate buffer (pH 7.0). Samples were prepared in a sample bu... |
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Bleach gel: a simple agarose gel for analyzing RNA quality.
Electrophoresis 33 , 366-369, (2012) RNA-based applications requiring high-quality, non-degraded RNA are a foundational element of many research studies. As such, it is paramount that the integrity of experimental RNA is validated prior to cDNA synthesis or other downstream applications. In the ... |