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  1. 原著論文

On-chip fraction collection for multiple selected ssDNA fragments using isolated extraction channels.

https://repo.qst.go.jp/records/46124
https://repo.qst.go.jp/records/46124
37103de6-4da1-4a1d-b754-59946779ff9e
Item type 学術雑誌論文 / Journal Article(1)
公開日 2011-07-14
タイトル
タイトル On-chip fraction collection for multiple selected ssDNA fragments using isolated extraction channels.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Li, Zheyu

× Li, Zheyu

WEKO 459201

Li, Zheyu

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Sun, Kai

× Sun, Kai

WEKO 459202

Sun, Kai

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Sunayama, Misato

× Sunayama, Misato

WEKO 459203

Sunayama, Misato

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Matsuo, Yasutaka

× Matsuo, Yasutaka

WEKO 459204

Matsuo, Yasutaka

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Vygantas, Mizeikis

× Vygantas, Mizeikis

WEKO 459205

Vygantas, Mizeikis

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Araki, Ryoko

× Araki, Ryoko

WEKO 459206

Araki, Ryoko

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Ueno, Kosei

× Ueno, Kosei

WEKO 459207

Ueno, Kosei

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Abe, Masumi

× Abe, Masumi

WEKO 459208

Abe, Masumi

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Misawa, Hiroaki

× Misawa, Hiroaki

WEKO 459209

Misawa, Hiroaki

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砂山 美里

× 砂山 美里

WEKO 459210

en 砂山 美里

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荒木 良子

× 荒木 良子

WEKO 459211

en 荒木 良子

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安倍 真澄

× 安倍 真澄

WEKO 459212

en 安倍 真澄

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抄録
内容記述タイプ Abstract
内容記述 High efficiency and high-purity fraction collection is highly sought in analysis of fragments-of-interest from selective polymerase chain reaction (PCR) products generated by High Coverage Gene Expression Profiling (HiCEP) methods. Here we demonstrate a new electrophoretic chip device enabling automatic high-efficient fractionation of multiple ssDNA target fragments during a run of separation. We used thoroughly isolated extraction channels for each selected target to reduce the risk of cross-contamination between targets due to cross-talk of extraction channels. Fragments of 35, 108 and 138 b, were successfully isolated, then the recovery was PCR-amplified and assessed by capillary electrophoresis (CE) analysis. Total impurity level of the targets due to unwanted fragments of 0.7%, 2% and 6% respectively, was estimated. Difficulties in collecting multiple target factions are due to band diffusion and DNA adsorption to the walls for the fragments in the separation channel, which is generated by transferring the DNA target fraction from the extraction section to the target reservoir. Therefore, we have carefully measured band broadening and analyzed its influence on the separation resolution due to the delay.
書誌情報 Journal of Chromatography A

巻 1218, 号 7, p. 997-1003, 発行日 2010-12
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-9673
DOI
識別子タイプ DOI
関連識別子 10.1016/j.chroma.2010.12.089
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