참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | L-Glutamine | HCID 5961 | — |
| 반응물 | PMA ionomycin | HCID 131724875 | — |
| 반응물 | HCID 178431920 | HCID 178431920 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | Ionomycin | HCID 6912226 | — |
반응 단계
The assay for PMA/ionomycin-stimulated PBMC proliferation was performed in 96-well flat bottomed microtitre plates. Compounds were prepared as 10 mM stock solutions in dimethyl sulfoxide. A 50-fold dilution of this was prepared in RPMI and serial dilutions were prepared from this solution. 10 μl of the 50-fold diluted stock, or dilutions of it, were added to the well to give concentrations in the assay starting at 9.5 μM and going down. Into each well was placed 1×105 PBMC, prepared from human peripheral blood from a single donor, in RPMI1640 medium supplemented with 10% human serum, 2 mM glutamine and penicillin/streptomycin. Phorbol myristate acetate (PMA) (0.5 ng/ml final concentration) and ionomycin (500 ng/ml final concentration) were added to these cells in supplemented RPMI1640 medium (as above) so that the final volume of the assay was 0.2 ml. The cells were incubated at 37° C. in a humidified atmosphere at 5% carbon dioxide for 72 hours. 3H-Thymidine (0.5 μCi) was added for the final 6 hours of the incubation. The level of radioactivity incorporated by the cells was then determined and this is a measure of proliferation.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07384950B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-3b904661dd2c4aa69e8d5b38aafb0227 |
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| 출처 메모 | uspto-grants-2008_06 |
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