Preparation of Affinity Column制备亲和层析柱【UCSF】
网站地图本站论坛
高级搜索收藏本站
  • Preparation of Affinity Column制备亲和层析柱【UCSF】

  • 点击:    作者:51protocol收集   来源: 日期:2007-03-23    本站论坛
Steven Finkbeiner, Departments of Neurology and Physiology, UCSF http://gweb1.ucsf.edu/labs/finkbeiner/Protocol/protocol_list/affiniry_col.CREB.shtml
  1. Add 222.2ul 1M MOPS, pH 7.5 to 2mL of 10mg of CREBtide (0.1M MOPS pH 7.5 final concentration).

  2. Read OD205, OD280 (using 0.1M MOPS buffer as blank)

  3. Affigel-10 is stored frozen at < -70糃. Thaw at 4糃 for ~20min.

  4. Filter 1-2mL on nylon (0.22uM poresize), using Buchner funnel and vacuum. Do not allow beads to dry.

  5. Wash bed with 3x2mL dH2O.

  6. Scrape 0.5-1mL into 15mL microfuge tube.

  7. Add 2.22ml CREBtide ligand solution to tube.
    Rock at 4糃 for 4hrs.

  8. Transfer slurry to column.

  9. Wash 2x500uL dH2O.

  10. Collect eluate and save at -20糃. Read OD.

  11. Wash column:
    • 2x5mL cold PBS
    • 1x5mL PBS/0.02% NaN3 (1uL NaN3 in5mL PBS)

  12. Store at 4糃 upright in beaker in PBS/NaN3 parafilm.


上一篇:GST fusion protein purification GST融合蛋白纯化   下一篇:Column Buffers: CREB

推荐文章
 
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