chip technology;
DNA;
concentration on-channel;
base stacking;
stacking;
D O I:
10.1016/j.chroma.2004.12.045
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
We evaluated a novel strategy for high-sensitivity DNA fragment analysis in a conventional glass double-T microfluidic chip. The microchip allows for a DNA on-channel concentration based on base stacking (BS) with a microchip capillary gel electrophoretic (MCGE) separation step in a poly(vinylpyrrolidone) (PVP) sieving matrix. Depending if low conductivity caused a neutralization reaction between the hydroxide ions and the run buffer component Tris(divided by). the stacking of DNA fragments were processed in the microchip. Compared to a conventional MCGE separation with a normal electrokinetic injection, the peak heights of 50-2650-base pair (bp) DNA fragments on the MCGE-BS separation were increased 3.9-8.0-fold. When we applied the MCGE-BS method to the analysis of a clinical sample of bovine theileria after PCR reaction, the peak height intensity of the amplified 816-bp DNA fragment from the I SS rRNA of T. buffeli was enhanced 7.0-fold compared to that of the normal injection method. (C) 2004 Elsevier B.V. All rights reserved.
机构:
Univ Tasmania, Sch Phys Sci Chem, Australian Ctr Res Separat Sci, Hobart, Tas 7001, AustraliaUniv Tasmania, Sch Phys Sci Chem, Australian Ctr Res Separat Sci, Hobart, Tas 7001, Australia
Tubaon, Ria Marni
Haddad, Paul R.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Tasmania, Sch Phys Sci Chem, Australian Ctr Res Separat Sci, Hobart, Tas 7001, AustraliaUniv Tasmania, Sch Phys Sci Chem, Australian Ctr Res Separat Sci, Hobart, Tas 7001, Australia
Haddad, Paul R.
Quirino, Joselito P.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Tasmania, Sch Phys Sci Chem, Australian Ctr Res Separat Sci, Hobart, Tas 7001, AustraliaUniv Tasmania, Sch Phys Sci Chem, Australian Ctr Res Separat Sci, Hobart, Tas 7001, Australia