Western blotting in Chlamydomonas reinhardtii

João Vitor Molino

Published: 2022-04-12 DOI: 10.17504/protocols.io.14egnjnpv5dy/v2

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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

1.

Centrifuge algae culture at 2000xg for 10 min1. Recover supernatant 0h 10m 0s

Sample preparation - Lysate

2.

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

3.

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

  1. Quantificate soluble protein 0h 15m 0s

Gel electrophoresis | SDS-PAGE

4.

Load 30 µg of total soluble protein (TSP) per lane in a 12% SDS-PAGE 1. Transfer proteins to a nitrocelulose membrane

  1. Block the membrane with 5% milk solution
  2. Probe the desired protein with the specific antibodie, diluted in 5% milk solution
  3. Wash 2 times with TBST (0.2 M Tris, 1.37 M NaCl, 0.1% Tween-20, pH 7.6)
  4. Add secondary antibody if required 30

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