Item type |
デフォルトアイテムタイプ_(フル)(1) |
公開日 |
2023-03-18 |
タイトル |
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タイトル |
Living cell positioning on the surface of gold film for SPR analysis |
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言語 |
en |
作成者 |
Yanase, Yuhki
Suzuki, Hidenori
Tsutsui, Tomoko
Uechi, Ichiro
Hiragun, Takaaki
Mihara, Shoji
Hide, Michihiro
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アクセス権 |
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アクセス権 |
open access |
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アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
権利情報 |
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権利情報 |
Copyright(c) 2007 Elsevier Advanced Technology |
主題 |
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主題Scheme |
Other |
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主題 |
biosensor |
主題 |
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主題Scheme |
Other |
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主題 |
surface plasmon resonance |
主題 |
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主題Scheme |
Other |
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主題 |
non-adherent cells |
主題 |
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主題Scheme |
Other |
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主題 |
cell fixation |
主題 |
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主題Scheme |
Other |
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主題 |
recovery |
主題 |
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主題Scheme |
NDC |
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主題 |
490 |
内容記述 |
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内容記述 |
Living cell reactions are detected as changes of the angle of resonance (AR) for surface plasmon resonance (SPR). Since SPR reflects the events in the field of evanescence, cells need to be fixed on the sensor chip. In this study, we developed methods to fix living cells on a gold surface and to recover adherent cells from the culture dish, preserving their functions to be analyzed by SPR. Human basophils and B cells were fixed to the sensor chip by a biocompatible anchor for cell membranes (alpha-succinimidyloxysuccinyl omega-oleyloxy polyoxyethylene), aminoalkanethiol (cyteamine, 8-amino octanethiol) or an amino-reactive cross-linker (dithiobis [succinimidylpropionate]). They showed an increase of AR in response to various stimuli. RBL-2H3 cells, which firmly adhered to the culture dish, were cultured/recovered with HydroCelI(TM)/Simple pipetting, with RepCelI(TM)/pipetting at 4 degrees C, or on normal plastic culture dishes with trypsinization or by scraping at 4 degrees C, respectively. The exocytosis of RBL-2H3 cells was largely impaired by scraping, but only slightly by the treatment with pipetting on HydroCell(TM), on RepCell(TM) or with trypsin. The membrane ruffling of the cells prepared by the last three treatments induced by antigens appeared the same. However, the change of AR with cells prepared by trypsin and those by scraping at 4 degrees C were lower than those by HydroCell(TM) or RepCell(TM), suggesting that trypsin may harm molecules involved in cellular reactions. Thus, the methods of cell fixation and removal with HydroCell(TM) or RepCell(TM) should enable us to analyze various reactions in either adherent or non-adherent cells by SPR. |
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言語 |
en |
出版者 |
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出版者 |
Elsevier Advanced Technology |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
出版タイプ |
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出版タイプ |
AO |
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出版タイプResource |
http://purl.org/coar/version/c_b1a7d7d4d402bcce |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
10.1016/j.bios.2007.07.005 |
関連情報 |
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関連タイプ |
isVersionOf |
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識別子タイプ |
DOI |
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関連識別子 |
http://dx.doi.org/10.1016/j.bios.2007.07.005 |
収録物識別子 |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
0956-5663 |
収録物識別子 |
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収録物識別子タイプ |
NCID |
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収録物識別子 |
AA10739666 |
開始ページ |
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開始ページ |
562 |
書誌情報 |
Biosensors & Bioelectronics
Biosensors & Bioelectronics
巻 23,
号 4,
p. 562-567,
発行日 2007-11
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旧ID |
21470 |