CN1712948A - Micro-fluid control chip electrophoretic detection of lipoprotein - Google Patents
Micro-fluid control chip electrophoretic detection of lipoprotein Download PDFInfo
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- CN1712948A CN1712948A CN 200510040296 CN200510040296A CN1712948A CN 1712948 A CN1712948 A CN 1712948A CN 200510040296 CN200510040296 CN 200510040296 CN 200510040296 A CN200510040296 A CN 200510040296A CN 1712948 A CN1712948 A CN 1712948A
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Abstract
An electrophoretic detection method of lipoprotein micro-fluid control chip includes pre-treating sample to obtain electrophoretic sample to be detected, add electrophoretic sample to be detected into chip electrophoresis apparatus for electrophoretic processing to obtain detecting peak of lipoprotein.
Description
Technical field:
The present invention relates to a kind of lipoprotein detection method.
Background technology:
Exist a large amount of ions, small molecular protein etc. to disturb the material of electric signal in the serum, existing method has and adopts first supercentrifugation to separate lipoprotein, after again its component is dialysed, carry out electrophoresis again and confirm lipoprotein component, such method program complexity, troublesome poeration.
Summary of the invention:
The object of the present invention is to provide a kind of easy to operate, the micro-fluid control chip electrophoretic detection of lipoprotein that step is easy.
Technical solution of the present invention is:
A kind of micro-fluid control chip electrophoretic detection of lipoprotein is characterized in that: comprise the following steps:
1. sample pre-service: will treat side serum 20 μ l and 80 μ l distilled waters, 50 μ l 0.1mg/mlNBD-ceramide (Chinese name: nitrobenzene-epoxy-azo-C6 acyl sphingosine; Sigma company product) mixing back 37 ℃ hatched 1 minute; lucifuge, refrigerator are preserved; add 250 μ l electrophoretic buffers before using; as electrophoresis sample to be measured
Described electrophoretic buffer is: 0.2mol/L Tricine (Chinese name: N-three (methylol) methylglycine, Sigma company product) 20ml and 0.1mol/L meglumin 40ml mix the back and add distilled water to 100ml, and transfer to PH10.1 with 1NNaOH;
2. will above-mentioned electrophoresis sample to be measured add in the chip electrophoresis instrument and carry out electrophoretic process, by negative pole positive pole extremely, sample introduction voltage is 600V to sample benzene at sample introduction with when separating, sample injection time is 30 seconds, separation voltage is 2000V, running temperature is 20 ℃, obtains the lipoprotein detected peaks.
Before electrophoretic process, earlier chip is handled: carry out prerunning with electrophoretic buffer earlier.
Step of the present invention is easy, easy to operate, and the signal to noise ratio (S/N ratio) of detection reaches about 15.
Fig. 1 is the electrophoresis result collection of illustrative plates of the embodiment of the invention 1.
Fig. 2 is the electrophoresis result collection of illustrative plates of embodiment 1.
Embodiment:
Embodiment 1:
A kind of micro-fluid control chip electrophoretic detection of lipoprotein comprises the following steps:
1. sample pre-service: will treat that side serum 20 μ l mix back 37 ℃ with 80 μ l distilled waters, 50 μ l 0.1mg/mlNBD-ceramide and hatched 1 minute, lucifuge, refrigerator are preserved, and add 250 μ l electrophoretic buffers before using, as electrophoresis sample to be measured,
Described electrophoretic buffer is: 0.2mol/L Tricine20ml and 0.1mol/L meglumin 40ml mix the back and add distilled water to 100ml, and transfer to PH10.1 with 1NNaOH;
2. before electrophoretic process, earlier chip is handled: carry out prerunning with electrophoretic buffer earlier.Then above-mentioned electrophoresis sample to be measured is added in the chip electrophoresis instrument and carry out electrophoretic process, sample benzene sample introduction when separating by negative pole to anodal, sample introduction voltage is 600V, sample injection time is 30 seconds, separation voltage is 2000V, and running temperature is 20 ℃, and whole electrophoresis time finished in 2 minutes, obtain the lipoprotein detected peaks, as shown in Figure 1.
Embodiment 2:
A kind of micro-fluid control chip electrophoretic detection of lipoprotein comprises the following steps:
1. sample pre-service: will treat that side serum 20 μ l mix back 37 ℃ with 80 μ l distilled waters, 50 μ l 0.1mg/mlNBD-ceramide and hatched 1 minute, lucifuge, refrigerator are preserved, and add 250 μ l electrophoretic buffers before using, as electrophoresis sample to be measured,
Described electrophoretic buffer is: 0.2mol/L Tricine20ml and 0.1mol/L meglumin 40ml mix the back and add distilled water to 100ml, and transfer to PH10.1 with 1NNaOH;
2. before electrophoretic process, earlier chip is handled: carry out prerunning with electrophoretic buffer earlier.Then above-mentioned electrophoresis sample to be measured is added in the chip electrophoresis instrument and carry out electrophoretic process, sample benzene sample introduction when separating by negative pole to anodal, sample introduction voltage is 600V, sample injection time is 30 seconds, separation voltage is 2000V, and running temperature is 20 ℃, carries out electrophoresis continuously 5 times, obtain the lipoprotein detected peaks, as shown in Figure 2.
Claims (2)
1, a kind of micro-fluid control chip electrophoretic detection of lipoprotein is characterized in that: comprise the following steps:
1. sample pre-service: will treat that side serum 20 μ l mix back 37 ℃ with 80 μ l distilled waters, 50 μ l 0.1mg/mlNBD-ceramide and hatched 1 minute, lucifuge, refrigerator are preserved, and add 250 μ l electrophoretic buffers before using, as electrophoresis sample to be measured,
Described electrophoretic buffer is: 0.2mol/LTricine20ml and 0.1mol/L meglumin 40ml mix the back and add distilled water to 100ml, and transfer to PH10.1 with 1NNaOH;
2. will above-mentioned electrophoresis sample to be measured add in the chip electrophoresis instrument and carry out electrophoretic process, by negative pole positive pole extremely, sample introduction voltage is 600V to sample benzene at sample introduction with when separating, sample injection time is 30 seconds, separation voltage is 2000V, running temperature is 20 ℃, obtains the lipoprotein detected peaks.
2, micro-fluid control chip electrophoretic detection of lipoprotein according to claim 1 is characterized in that: before electrophoretic process, earlier chip is handled: carry out prerunning with electrophoretic buffer earlier.
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CNB2005100402960A CN100357730C (en) | 2005-05-27 | 2005-05-27 | Micro-fluid control chip electrophoretic detection of lipoprotein |
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CNB2005100402960A CN100357730C (en) | 2005-05-27 | 2005-05-27 | Micro-fluid control chip electrophoretic detection of lipoprotein |
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CN1712948A true CN1712948A (en) | 2005-12-28 |
CN100357730C CN100357730C (en) | 2007-12-26 |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101017176B (en) * | 2007-02-08 | 2011-07-27 | 南通大学附属医院 | Method for detecting small and dense low density lipoprotein with microflow hole chip electrophoretic separation |
CN101614696B (en) * | 2009-07-06 | 2012-03-07 | 南通大学附属医院 | Method for high-density lipoprotein chip electrophoresis |
CN101498630B (en) * | 2008-01-30 | 2012-06-27 | 中国科学院电子学研究所 | Sample pretreatment integrated chip |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4167467A (en) * | 1977-09-21 | 1979-09-11 | Helena Laboratories Corporation | Clinical procedure for measuring lipoprotein free cholesterols |
FR2533704B1 (en) * | 1982-09-27 | 1986-03-21 | Spiral | IMMUNOLOGICAL ASSAY IN THE SERUM OF APOLIPOPROTEIN B OF LOW DENSITY LIPOPROTEINS |
RU2128835C1 (en) * | 1996-04-01 | 1999-04-10 | Центральный научно-исследовательский институт гастроэнтерологии | Method for diagnosing hepatic cholestasis by means of blood serum lipoprotein electrophoresis |
CN1223856C (en) * | 2002-07-18 | 2005-10-19 | 中国科学院大连化学物理研究所 | Microflow control chip for protein analysis and its application in protein analysis |
CN1548546A (en) * | 2003-05-09 | 2004-11-24 | 中国科学院大连化学物理研究所 | Continuous unicellular inclusion analyzing method based on microflow control chip platform |
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2005
- 2005-05-27 CN CNB2005100402960A patent/CN100357730C/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101017176B (en) * | 2007-02-08 | 2011-07-27 | 南通大学附属医院 | Method for detecting small and dense low density lipoprotein with microflow hole chip electrophoretic separation |
CN101498630B (en) * | 2008-01-30 | 2012-06-27 | 中国科学院电子学研究所 | Sample pretreatment integrated chip |
CN101614696B (en) * | 2009-07-06 | 2012-03-07 | 南通大学附属医院 | Method for high-density lipoprotein chip electrophoresis |
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