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  1. 医歯学総合研究科
  2. 医歯学総合研究科・学術誌論文

Cold in-situ-hybridization of human T-cell leukemia virus type 1: Production of biotinylated probes by polymerase chain reaction and improvement of procedures

http://hdl.handle.net/10232/3739
http://hdl.handle.net/10232/3739
8ad04069-7623-4186-a679-313b1cf60c96
名前 / ファイル ライセンス アクション
DC(Hasui)1995.pdf DC(Hasui)1995.pdf (3.4 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2010-04-13
タイトル
タイトル Cold in-situ-hybridization of human T-cell leukemia virus type 1: Production of biotinylated probes by polymerase chain reaction and improvement of procedures
著者 Hasui, Kazuhisa

× Hasui, Kazuhisa

WEKO 116879

Hasui, Kazuhisa

Search repository
Sato, Eiichi

× Sato, Eiichi

WEKO 116880

Sato, Eiichi

Search repository
Sueyoshi, Kazunobu

× Sueyoshi, Kazunobu

WEKO 116881

Sueyoshi, Kazunobu

Search repository
Kitajima, Shinichi

× Kitajima, Shinichi

WEKO 116882

Kitajima, Shinichi

Search repository
Goto, Masamitsu

× Goto, Masamitsu

WEKO 116883

Goto, Masamitsu

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Nakamura, Takao

× Nakamura, Takao

WEKO 116884

Nakamura, Takao

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Matsumoto, Daiten

× Matsumoto, Daiten

WEKO 116885

Matsumoto, Daiten

Search repository
言語
言語 eng
キーワード
主題Scheme Other
主題 HTLV-1
キーワード
主題Scheme Other
主題 DNA-DNA cold in-situ-hybridization
キーワード
主題Scheme Other
主題 DNA-RNA cold-in-situ-hybridization
キーワード
主題Scheme Other
主題 MT-2
キーワード
主題Scheme Other
主題 biotinylated double-stranded DNA probes
キーワード
主題Scheme Other
主題 polymerase chain reaction
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
要約(Abstract)
内容記述タイプ Other
内容記述 In order to detect histochemically signals of human T-cell leukemia virus type 1 (HTLV-1) proviral DNA and its proviral DNA in MT-2 cells, we made highly biotinylated probes corresponding to parts of HTLV-1 proviral DNA by means of 2 times polymerase chain reaction (PCR) and improved the procedures of DNA-RNA and DNA DNA cold in-situ-hybridization (cISH) for HTLV-1. We produced 7 highly biotinylated double-stranded DNA probes for the long terminal repeat, gag-pol region, env region and pX tax and rex regions of HTLV-1. DNA-RNA cISH of these probes was established, evaluating the effect of 17% polyvinyl alcohol solvent for reducing non-specific alkaline phosphatase reaction in the process of visualizing hybridized probe and suggesting the necessary prehybridization incubation with hybridization buffer containing salmon DNA for diminishing non-specific binding of probes with tissue. On the other hand, DNA-DNA cISH of a cocktail of these 7 probes could show only too faint dot-like stain in nuclei to be applied to a study of HTLV-l-related lesions, denaturing DNA in sections and probes in aluminum box for 10 min at 200℃, incubating the sections with probes for hybridization for 3 days at 45℃ and performing overnight alkaline phosphatase reaction by using 17 % polyvinyl alcohol solvent after streptavidine-biotinylated alkaline phosphatase system to detect the hybridized probes.
収録雑誌名 Dendritic cells

巻 5, p. 27-35
作成日
日付 1995-01-01
NII書誌ID(雑誌)
収録物識別子タイプ NCID
NC ID AA11039557
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
NDC
主題Scheme NDC
主題 490
NIIsubject
主題Scheme Other
主題 医学
公開者・出版者
出版者 日本樹状細胞研究会
公開者別名
公開者別名 Japanese Dendritic Cells Society
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