| 查看: 1430 | 回复: 5 | |||
| 当前只显示满足指定条件的回帖，点击这里查看本话题的所有回帖 | |||
[求助]
乳酸菌电转 已有1人参与
|
|||
|
求助各位大神有没有知道乳酸乳球菌MG1363感受态的具体做法及原理，和电转方法及原理！谢谢！ @youlinglyw @wizardfan @biostar2009 发自小木虫Android客户端 |
回复此楼» 猜你喜欢
不合理蛙科研实验之小鼠实验：严谨设计，解析生命机制的重要载体
已经有0人回复
-
不合理蛙科研实验之重金属检测：精准筛查，守护健康与环境的防线
已经有0人回复
-
化学工程及工业化学论文润色/翻译怎么收费?
已经有294人回复
-
不合理蛙科研实验之“蛙测重金属我背锅三千”
已经有0人回复
-
不合理蛙科研实验之“鼠逃三次我发三篇SCI”
已经有0人回复
-
纳米粒度分析
已经有3人回复
-
林科院林化所招收材料与化工专业硕士，坐标南京
已经有0人回复
-
留学--博士招生
已经有16人回复
-
化学工程，本211，求调剂，ab区不限
已经有4人回复
-
邵阳学院食品与化学工程学院硕士调剂
已经有0人回复
WilliamHJ
金虫 (小有名气)
- 应助: 8 (幼儿园)
- 金币: 2186.9
- 红花: 5
- 帖子: 170
- 在线: 58.5小时
- 虫号: 1858225
- 注册: 2012-06-13
- 性别: GG
- 专业: 生物物理、生物化学与分子
【答案】应助回帖
★ ★ ★
西门吹雪170: 金币+3, 鼓励回帖交流 2020-03-11 08:06:52
西门吹雪170: 金币+3, 鼓励回帖交流 2020-03-11 08:06:52
|
Preparation of the cells: Day 1: Inoculate 5 ml of G/L-SGM17B medium with L. lactis glycerol stock from -80 C and grow at 30 C, without aeration, overnight Day 2: Inoculate 50 ml of G/L-SGM17B with pre-culture in a dilution of 1:100 and grow at 30 C, without aeration, overnight Day 3: - Add 50 ml full-grown culture to 400 ml of G/L-SGM17B medium - Grow the culture until OD600 is 0.2-0.3 (ca. 3 h) - Spin down cells for 20 min at 6000 x g, 4 C - Wash cells with 400 ml of 0.5 M sucrose, 10% glycerol (4 C) and spin down at 6000 x g (centrifugation speed may need to be increased during successive washing steps) - Resuspend the cells in 200 ml of 0.5 M sucrose, 10% glycerol, 50 mM EDTA (4 C), keep the suspension on ice for 15 min and spin down - Wash cells with 100 ml of 0.5 M sucrose, 10% glycerol (4 C) and spin down (6000 x g) - Resuspend the cells in 4 ml of 0.5 M sucrose, 10% glycerol (4 C): Use 40 μl per electroporation (keep on ice) Or store the cells in small portions at -80 C, let them defreeze on ice before use Electroporation: - Place 40 μl cells in a pre-chilled electroporation cuvette with 1 μl DNA (100-500 ng vector DNA reconstituted in TE-, Tris-buffer, or distilled water; for transforming cells with ligation product use 500-1000 ng DNA) and keep the cuvette on ice - Use Biorad Genepulser with following adjustments: 2000 V 25 μF 200 Ω - Pulse (normal reading is 4.5-5 msec) - Add 1 ml of G/L-M17B + 20 mM MgCl2 + 2 mM CaCl2 - Keep the cuvette for 5 min on ice and incubate 1-1.5 h at 30 C - Plate 10 μl, 100 μl, 900 μl on M17agar with glucose or lactose and antibiotics (depends on plasmid) - Incubate 1-2 days at 30 °C Materials: - G/L-SGM17B: M17-Broth with: 0.5 M sucrose 2.5% glycine 0.5% glucose or 0.5% lactose (strain dependent) Add the sucrose and glycine to the M17-B and sterilize 20 min 121 °C. Add sterile glucose or lactose after cooling down. - 0.5 M sucrose/ 10% glycerol - 0.5 M sucrose/ 10% glycerol/ 0.05 M EDTA L. lactis grows very slowly on G/L-SGM17B. Leaving out the sucrose is possible (Wells et al., 1993) but can decrease the transformation efficiency. The medium for cell recovery must contain MgCl2 and CaCl2. 我用这个protocol做的，效果还不错 |
5楼2020-03-10 11:17:16
2楼2019-06-16 11:15:32
3楼2019-08-09 22:34:26
4楼2019-08-09 22:36:05
