Western blotting in Chlamydomonas reinhardtii
João Vitor Molino
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Abstract
This protocols describe the steps to perform a western blot in Chlamydomonas reinhardtii cell lysate and supernatant samples.
Before start
Check antibody dilutions* Check buffers disponibility
- Prepare 5% milk solution
Steps
Sample preparation - Supernatant
Centrifuge algae culture at 2000xg for 10 min1. Recover supernatant
0h 10m 0s
Sample preparation - Lysate
Centrifuge algae culture at 2000xg for 10 min1. Remove supernatant, and re-suspend cells in lysis buffer (50 mM Tris·HCL (pH 8.0), 0.1% Triton X-100), concentrating cells 100-fold.
0h 10m 0s
Sonication
Sonicate using appropriate sonication tip. Duty cycle: 0.5 | Cycle: 1.0 s | Amplitude: 20% | Duration: 30 s1. Centrifuge for 15 min at 20000xg to remove cells debries and recover soluble proteins
- Quantificate soluble protein
0h 15m 0s
Gel electrophoresis | SDS-PAGE
Load 30 µg of total soluble protein (TSP) per lane in a 12% SDS-PAGE 1. Transfer proteins to a nitrocelulose membrane
- Block the membrane with 5% milk solution
- Probe the desired protein with the specific antibodie, diluted in 5% milk solution
- Wash 2 times with TBST (0.2 M Tris, 1.37 M NaCl, 0.1% Tween-20, pH 7.6)
- Add secondary antibody if required
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