1. 日本VA视频,综合福利导航,麻豆熟妇乱妇熟色A片在线看,你懂的国产在线,97香蕉久久国产超碰青草专区,狼友福利在线,久久99免费麻辣视频,影音先锋成人网站
          English | 中文版 | 手機版 企業登錄 | 個人登錄 | 郵件訂閱
          當前位置 > 首頁 > 技術文章 > Primary brain cell isolation and culture

          Primary brain cell isolation and culture

          瀏覽次數:2431 發布日期:2011-6-13  來源:www.pricells.com.cn
                                         Primary brain cell isolation and culture.  

          1. Cerebella were removed from 7-day-old mice and passed through Nitex nylon netting (80 μm pore size) into primary cell system containing 20% (v/v) fetal calf serum (FCS).

          2. The cell suspension was plated at a density of four cerebella per 12-well culture plate.

          3. Primary cell culture system was changed two days after plating and twice a week thereafter, gradually decreasing the FCS concentration to 10%.

          4. At 14 days in culture, dibutyryl-cAMP was added to the medium for 1 week to promote the morphological differentiation of astrocytes.

          5. Experiments were performed on 3-week-old cultures.

          6. Cortical astrocytes were prepared from 1-day-old mice following the same procedure used for cerebellar astrocytes plated at a density of two cortices per 12-well culture plate.

          7. Cerebellar neurons were isolated and cultured from the cerebellum of 7-day-old mice, after mild trypsinization of the tissue followed by trituration in a DNase solution containing a trypsin inhibitor derived from soybeans.

          8. Cells were suspended in a slightly modified primary cell culture containing 50 μM kainic acid and 10% (v/v) FCS and plated at density 2 × 106 cells per well in a 12-well culture plate.

          9. The wells had been coated with poly-L-lysine.

          10. Cytosine arabinoside (20 μM) was added after 48 h to prevent astrocyte proliferation.

          11. Cells were used for experiments after 1 week in culture.

          12. For the co-cultures, the neurons and astrocytes were prepared separately and seeded as described earlier.

          13. The astrocytes were cultured on inserts for 21 days, and the neurons were cultured in culture plates for 7 days prior to incubation in co-culture.

          14. The astrocytes were grown on permeable membranes in tissue culture plate inserts, and the neurons were cultured in standard tissue culture plates.

          15. The inserts were transferred to the neuronal plates 24 h prior to incubation.

          16. At time of insert transfer, half of the neuronal medium was extracted and replaced with astrocyte cell culture system.

          發布者:武漢原生原代生物醫藥科技有限公司
          聯系電話:027-87490190
          E-mail:service@pricells.com.cn

          標簽: Primary brain cell
          用戶名: 密碼: 匿名 快速注冊 忘記密碼
          評論只代表網友觀點,不代表本站觀點。 請輸入驗證碼: 8795
          Copyright(C) 1998-2025 生物器材網 電話:021-64166852;13621656896 E-mail:info@bio-equip.com
          主站蜘蛛池模板: 婷婷久久久| 欧美性猛交99久久久久99按摩| 亚洲中文字幕久久精品无码喷水| 蜜臀午夜一区二区在线播放| 黄总av| 激情五月久久| 337p西西人体大胆瓣开下部| 一个人看的www日本高清视频 | 国内老熟妇对白hdxxxx| 国产成人精品97| 日韩十八不禁| 无码人妻丝袜| 国产人与禽zoz0性伦多活几年| 精品国产人妻一区二区三区| 高清dvd碟片 生活片| 国产熟女网站| 亚洲口爆| 被c到高潮疯狂喷水国产| 中文字幕日韩精品人妻| 尤物av在线| 巴林左旗| 亚洲国产成人极品综合| 免费看无码自慰一区二区| 一区二区三区精品| 国产资源网| 亚洲日韩av在线观看| 亚洲精品一区中文字幕乱码| 日本边添边摸边做边爱| 免费看欧美成人A片无码| www.jizz国产| 国产95在线 | 欧美| 欧美肥老太交视频免费| 懂色av,蜜臀AV粉嫩av| 南川市| 男人的天堂av社区在线| 国产普通话对白刺激| 在线无码| 固原市| 人妻有码av中文字幕久久琪| 亚洲成年| 亚洲人成网站色7799|