链霉亲和素结合物

Chlamydomonas Fixation for Transmission Electron Microscopy

Solutions:

Chlamydomonas culture medium + 2% glutaraldehyde (5 ml medium + 0.9 ml 25% glutaraldehyde

100 mM sodium cacodylate, pH 7.2

1% glutaraldehyde in 100 mM sodium cacodylate, pH 7.2

1% OsO4 in 100 mM sodium cacodylate

Method:

  1. Dilute cells suspended in culture medium into an equal volume of 2% glutaraldehyde in culture medium. Transfer cells to a 15 ml conical polypropylene centrifuge tube. Fix for 15-20 min, room temp.
  2. Gently pellet cells in the clinical centrifuge (2 min setting #6).
  3. Remove supernatant and gently suspend cells in 1% glutaraldehyde in 100 mM sodium cacodylate. Fix 1 hour at room temperature and overnight at room temp 4 degrees C.
  4. Gently pellet cells, remove supernatant, and suspend in 100 mM sodium cacodylate. Repeat this for a total of 4 washes, 2-5 min each wash.
  5. Suspend cells in 1% OsO4 in 100 mM sodium cacodylate and fix for 1 hour.
  6. Gently pellet cells and resuspend in distilled water. Wash 2-3 times with water.
  7. Suspend cells in 1% uranyl acetate in water. Stain 1 hr to overnight at room temp.
  8. Dehydrate cells in acetone. I usually suspend cells in 25% acetone:75% water for ~5 min, let the cells settle or gently centrifuge to lightly pellet cells. Remove the supernate and suspend cells in 50:50 acetone:water for 5 min. Repeat washes with 75%, and two 100% acetone changes.
  9. Embed in Epon resin.

Suspend cells in 1/3 plastic:2/3 acetone and leave the tube uncovered overnight in the hood. If possible, put the tubes on a rotary shaker. The acetone will gradually evaporate and increase the concentration of plastic.

The next day gently pellet the cells, remove the acetone:plastic mix and add fresh 100% plastic. I generally underlay the cells with plastic, let them sit for ~30 min, and place the tubes in a vacuum chamber - pumped by house vacuum. Cells will settle to the bottom of the tube within 1-2 hrs. Pellet the cells in the clinical centrifuge and remove the plastic above the cells.

Put BEEM capsules in the bottom of plastic or glass centrifuge tubes, fill about half full with fresh plastic, and overlay with cells from the above pellets. Spin at top speed for ~ 10 min. Put a label in the top of the capsule and put the tubes in the oven.

Polymerize at 40 degrees C overnight and raise to 65-80 degrees C for a second day or just put at 65 degrees C for 1-2 days.

================  蚂蚁淘在线  ================

免责声明:本文仅代表作者个人观点,与本网无关。其创作性以及文中陈述文字和内容未经本站证实,对本文以及其中全部或者部分内容、文字的真实性、完整性、及时性本站不做任何保证或承诺,请读者仅作参考,并请自行核实相关内容

版权声明:未经蚂蚁淘在线授权不得转载、摘编或利用其他方式使用上述作品。已经经本网授权使用作品的,应该授权范围内使用,并注明“来源:蚂蚁淘在线”。违反上述声明者,本网将追究其相关法律责任。