Difference between revisions of "C4Dマイクロチップ電気泳動のアニオン検出"

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(Equipment and Reagents Required)
(必要な装置と試薬)
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** [Http://www.edaq.com/ER225 ER225 C4D データシステム]
 
** [Http://www.edaq.com/ER225 ER225 C4D データシステム]
 
** [http://www.edaq.com/ET225 ET225 マイクロチッププラットフォームj]
 
** [http://www.edaq.com/ET225 ET225 マイクロチッププラットフォームj]
** [http://www.edaq.com/ER230_HV-Sequencer ER230 High Voltage Sequencer] (one or two units)
+
** [http://www.edaq.com/ER230_HV-Sequencer ER230 高電圧シーケンサー] (1または2台)
** [http://www.edaq.com/ET145-4 ET145-4 CE Microchip (45 mm) kit]
+
** [http://www.edaq.com/ET145-4 ET145-4 CE マイクロチップ(45 mm) ]
** [http://www.edaq.com/ES280 PowerChrom] and [http://www.edaq.com/locked/software/sequencer.php Sequencer] softwares
+
** [http://www.edaq.com/ES280 PowerChrom] 及び [http://www.edaq.com/locked/software/sequencer.php Sequencer] ソフトウェア
 
* Background Electrolyte (BGE) = 70 mM TRIS/CHES with 1ppm HDMB, where TRIS is Tris(hydroxymethyl)aminomethane, CHES is 2-(Cyclohexylamino)ethanesulfonic acid, and HDMB is hexadimethrine bromide  
 
* Background Electrolyte (BGE) = 70 mM TRIS/CHES with 1ppm HDMB, where TRIS is Tris(hydroxymethyl)aminomethane, CHES is 2-(Cyclohexylamino)ethanesulfonic acid, and HDMB is hexadimethrine bromide  
 
* Samples = 100 μM and 10 μM Cl<sup>-</sup>, NO<sub>3</sub><sup>-</sup> and HSO<sub>4</sub><sup>-</sup> in deionised water.
 
* Samples = 100 μM and 10 μM Cl<sup>-</sup>, NO<sub>3</sub><sup>-</sup> and HSO<sub>4</sub><sup>-</sup> in deionised water.

Revision as of 12:43, 28 February 2014

図 1. マイクロチップ
図 2. 100 μM  Cl-, NO3- 、HSO4- のエレクトロフェログラム
図 3. 10 μM Cl-, NO3-, HSO4- のエレクトロフェログラム

非接触電導度検出器を用いてマイクロチップ電気泳動によって三種類の無機アニオンの検出に eDAQ C4D システムが使われています。

はじめに

三種類の無機陰イオン Cl-, NO3- 、及び HSO4- をマイクロチップ電気泳動法 (MCE) を使って分離し、 eDAQ C4D システムで検出します。

必要な装置と試薬

Time (s) Step sample BGE waster outlet
0-20 loading -1000V -700V 0V -1000V
20-60 separation -750V -1000 V -750V 0V

Data Analysis and Limit of Detection

Figure 2 shows the electropherogram of the 100 μM Cl-, NO3- and HSO4- solution. In order to measure the limit of detection of the anions, a 10 μM solution of the same analytes was analyzed. The electropherogram is shown in Figure 3.

Using the definition of limit of detection as equal to three times the standard deviation of signal (during four seconds before the first peak), the limit of detection is 3.7 μM for Cl- and NO3-, and 1.3 μM for HSO4-.