Difference between revisions of "20211101 Restart"
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[https://wiki.uio.no/mn/fysikk/laglivlab/images/2/22/Suggested_Procedure_for_Coating_Cell_Cultureware.pdf protocol for coating with fibronectin] and an [https://wiki.uio.no/mn/fysikk/laglivlab/images/d/d5/Alternativ_protokoll.pdf alternative protocol]. | [https://wiki.uio.no/mn/fysikk/laglivlab/images/2/22/Suggested_Procedure_for_Coating_Cell_Cultureware.pdf protocol for coating with fibronectin] and an [https://wiki.uio.no/mn/fysikk/laglivlab/images/d/d5/Alternativ_protokoll.pdf alternative protocol]. | ||
− | The first recommends 2-10 mg/cm^2, the alternative protocol recommends 1-5 | + | The first recommends 2-10 mg/cm^2, the alternative protocol recommends 1-5 ug/cm^2. We need Tris buffer. Balance and weighing equipment is found in lab 420. |
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Revision as of 13:17, 2 November 2021
Contents
Restart of project
New microscope glass, microfluidic preparation
On Oct 28 2021 Anniken, Adam, Endre and Thomas went to Lab 128 and... PDMS on... Fill in!!
New microscope glass, cells for test
Cells
New microscope glass, cells in microfluidic
Describe experiment
On Oct 29 2021 Anniken's update on the timelapse. The cells did not adhere, but the PDMS was still properly attached to the glass slide. Maybe plasma cleaning the adhesive slides disturbes the cell adhesive properties? Anyway, only plasma cleaning the PDMS didn’t work either. We could try one more time when we have more cells just to be sure or try using fibronectin.
Suggestions for continuation using fibronectin
Anniken has found a protocol for coating with fibronectin and an alternative protocol.
The first recommends 2-10 mg/cm^2, the alternative protocol recommends 1-5 ug/cm^2. We need Tris buffer. Balance and weighing equipment is found in lab 420. ...