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  1. 川崎医学会機関誌
  2. Kawasaki Medical Journal
  3. Vol.9(1983)
  4. No.4

Growth Characteristics of KB and RAJI Cells in the Liquid Culture Medium in Relation to the Human Tumor Stem Cell Assay for Anti-Tumor Agents

https://kwmed.repo.nii.ac.jp/records/99
https://kwmed.repo.nii.ac.jp/records/99
1248364b-29ea-4979-a4bd-6a75ea6fa925
名前 / ファイル ライセンス アクション
KJ00010229739.pdf KJ00010229739.pdf (643.7 kB)
Item type [ELS]学術雑誌論文 / Journal Article(1)
公開日 2017-01-23
タイトル
タイトル Growth Characteristics of KB and RAJI Cells in the Liquid Culture Medium in Relation to the Human Tumor Stem Cell Assay for Anti-Tumor Agents
言語 en
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
著者 WATANABE, Satoru

× WATANABE, Satoru

en WATANABE, Satoru

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SAITO, Taiichi

× SAITO, Taiichi

en SAITO, Taiichi

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NOHNO, Tsutomu

× NOHNO, Tsutomu

en NOHNO, Tsutomu

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著者所属(英)
en
Department of Pharmacology, Kawasaki Medical School
著者所属(英)
en
Department of Pharmacology, Kawasaki Medical School
著者所属(英)
en
Department of Pharmacology, Kawasaki Medical School
キーワード
言語 en
主題Scheme Other
主題 KB cells
キーワード
言語 en
主題Scheme Other
主題 RAJI cells
キーワード
言語 en
主題Scheme Other
主題 cancer chemotherapy
キーワード
言語 en
主題Scheme Other
主題 in vitro assay
キーワード
言語 en
主題Scheme Other
主題 Coulter Counter
記事種別(英)
内容記述タイプ Other
内容記述 Original Article
言語 en
抄録(英)
en
Recently the chemosensitivity assay with clonal human tumor stem cells in liquid medium have been developed. We have investigated the optimal conditions for culture and counting of KB cells, which derived from a human epidermoid carcinoma and grow as a sheet adhered to the bottom surface of the culture, and RAJI cells, which derived from Burkitt lymphoma and grow as a suspension in liquid medium, as the representatives of the human tumor cells. Both stock cells were maintained in Eagle's MEM medium plus 10 per cent calf serum in C02 incubator at 37°C. Trypsinized cell suspensions were delivered in plastic wells with different culture media and incubated for different periods. Then the cell number was counted by the Coulter Counter in ISOTON II solvent. For KB cells, the culture medium should not be changed for 72 hours, otherwise enough cell number could not be obtained. To prevent the aggregation of KB cells in ISOTON II, calf serum (10%) was effective and EDTA (0.02%) had an additive effect. RAJI cells did not aggregate in ISOTON II. Ethanol and dimethylsulfoxide inhibited the growth of RAJI cells, but almost no inhibition was noted when the initial cell number was more than 8×l04/ml. Ethanol was more toxic. Both solvents, however, did not affect the growth of KB cells.
書誌情報 en : Kawasaki medical journal

巻 9, 号 4, p. 239-245, 発行日 1983
URL
識別子 http://igakkai.kms-igakkai.com/wp/wp-content/uploads/1983en/9(4)239-245.1983.pdf
識別子タイプ URI
DOI
識別子タイプ DOI
関連識別子 https://doi.org/10.11482/KMJ-E9(4)239
ISSN
収録物識別子タイプ PISSN
収録物識別子 0385-0234
ISSN
収録物識別子タイプ EISSN
収録物識別子 2434-3404
雑誌書誌ID
収録物識別子タイプ NCID
収録物識別子 AA00710169
雑誌書誌ID
収録物識別子タイプ NCID
収録物識別子 AA12029005
著者版フラグ
出版タイプ VoR
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