Yu:Lysis: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
m (span)
mNo edit summary
Line 15: Line 15:
{| border="0" cellpadding="5" style="width:50%"
{| border="0" cellpadding="5" style="width:50%"
|+ '''Completed <span id="buffer">lysis buffer</span> for one fastprep tube'''
|+ '''Completed <span id="buffer">lysis buffer</span> for one fastprep tube'''
|align="left"|600μL 1x [[Yu:PBS#PBSMT|PBSMT]]
|align="left"|Per 1mL 1x [[Yu:PBS#PBSMT|PBSMT]]
|-
|-
|3μL 200mM [[PMSF]]
|5μL / mL 200mM [[PMSF]]
|-
|-
|1.56μL .5M Benzamide
|2.6μL / mL .5M Benzamide
|-
|-
|0.6μL [[Yu:PLAAC|PLAAC]]
|1μL /mL [[Yu:PLAAC|PLAAC]]
|}
|}
|-
|-

Revision as of 17:19, 17 December 2009

Home       Procedures       | Lab Members       | Publications       | Research Interests       | Internal Database      


Quick Yeast Lysis Procedure
1. Grow yeast cells to late-log phase Grow yeast
2. Pellet 2mL cell culture in fast-prep tube. Remove excess supernatant. 2mL yeast culture pelleted in fastprep tube
3. Prepare 600μL completed yeast lysis buffer per fastprep tube. Multiply each ingredient by the number of fastprep tubes to be lysed. Keep on ice after prepared and while using. Prep completed lysis buffer per tube:
Completed lysis buffer for one fastprep tube
Per 1mL 1x PBSMT
5μL / mL 200mM PMSF
2.6μL / mL .5M Benzamide
1μL /mL PLAAC
4. Add 100μL complete lysis buffer to each fastprep tube. Keep on ice or in cold room for remaining steps. 100μL comp. lysis buffer per tube
5. Add approximately 100μL acid-washed glass fastprep beads to each tube. 100μL beads per tube
6. Fastprep at 6.5 m/s for 30 seconds Fastprep at 6.5 for 30s
7. Add 500μL completed lysis buffer to each fastprep tube 500μL comp. lysis buffer per tube
8. Spin at top speed for 10 minutes at 4°C Spin top speed 10 minutes at 4°C
9. Pipette off supernatant, which contains lysates. Store on ice or in -20°C freezer. Remove and save supernatant