Preparation of Competent Cells (from PMB)
网站地图本站论坛
高级搜索收藏本站
 
 当前位置:试验方案>核酸试验>DNA试验>克隆> 正文

Preparation of Competent Cells (from PMB)

点击:   作者:51protocol收集   来源:  时间: 2007-03-25  本站论坛

Preparation of Competent Cells (from PMB)

  1. Inoculate a couple of 20 ml LB broth in a 125 ml flasks with 0.5 ml of an overnight culture of the recipient strain.
  2. Shake at 37 C until O.D. 600=0.13 - 0.15 (1 - 2 hours). Measure by taking some of the broth out with a sterile DPTP and reading in a plastic cuvette (discard cells afterward): If flanking arm flasks are accessible, use them for measuring O.D.
  3. Spin the cells in sterile Oak Ridge Tube (5 K, 5 min, 4 C) and resuspend in 1 ml PMB #A. Then add another 9 ml PMB #A and spin the cells again (5 K, 5 min, 4 C).
  4. Decant and resuspend in 1 ml PMB #B. Then add 9 ml more PMB #B.
  5. Let sit on ice for 30 min, spin as above and resuspend in 2 ml PMB #B, add 0.2 ml glycerol and 30 µl DMSO. Use fresh or freeze in dry ice/EtOH.

PMB #A
1X 200 ml 1X
10 mM MOPS pH 7.0 210 mg Free acid
230 mg Na salt
10 mM Rubidium chloride 240 mg
Autoclave and store at 4 C
PMB #B
1X 200 ml 1X
10 mM MOPS pH 6.5 350 mg Free acid
85 mg Na salt
50 mM Calcium chloride 1.12 g
10 mM Rubidium chloride 240 mg
Autoclave and store at 4 C


上一篇:ELECTROPORATING E. COLI   下一篇:Transformation of E. coli by Electroporation [Stanford University]

 
推荐文章
·找质粒.载体图谱及序列的方法
·分子克隆的常用工具酶
·大肠杆菌感受态细胞制备及转化中的影响因素
·重组DNA技术与基因工程
·分子克隆常用技术
·质粒DNA的限制性内切酶酶切分析
·基因克隆的几种常用方法
·基因克隆:高效感受态细胞制作
相关文章
推荐专题
 


↑返回顶部   打印本页   关闭窗口↓  
 本站申明 联系我们 网站地图
Copyright© 试验方案

Powered by DedeCms email:htmyth#yahoo.com.cn

Optimized to 1024x768 to Firefox,Opera and MS-IE6