细胞分离

7 3D Assay in Matrigel : S1, T42, T42R

(Writtenfor35mmdishes?ifsmallerdishesareused,volumesofmatrigelmustbeadjustedtocorrectforthetendencyofmatrigeltoadheretothesidesofthedish.)

  1. Pre-coat35mmdishwith200to300microlitersofmatrigel.
  2. Placedishin37oCincubatorfor10to15minutesandallowmatrigeltopolymerize.
  3. duringpolymerizationofthematrigel,trypinsizecells.
  4. Pellet0.6to1.2x106cells,aspiratemedia,flicktubetobreakuppellet.?
    1. S1cells

1.0x106cells/1.2mlmatrigel

    1. T4-2.

0.7x106cells/1.2mlmatrigel.

    1. T4-2+AIIBII

0.7x106cells/1.2mlmatrigel

    1. T4-2+

  1. Onice,add1.2mlmatrigeltotube.
  2. CarefullyPipetteupanddowntodistributecellsbutnotintroducebubblesintothematrigel.
  3. Transfermatrigelandcellmixturetopre-coated35mmdish.
  4. Placein37oCincubatorfor15to30minutesandallowmatrigeltopolymerize.
  5. Oncegelisformed,add1.5to2.0mlmediatodish.
    1. ForS1:H14+EGFmedium
    2. ForT4-2:H14medium
    3. TorevertT4-2withtyrophorstin:H14medium+tyrophorstin80nM

  1. Wegrowourcellsfor10daystoallowspheroidstoform;changingmediaevery2to3days.

================  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。