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ABE Summer Workshop 2005 Southern & Western Blotting Goals with Southern Blot Using specific PDI gene probes: • Identify PDI genes in wild type Arabidopsis plants. • Determine the status of PDI genes in T-DNA Arabidopsis mutants. Southern Blot Process 1. Restriction digestion: breaks up DNA. 2. Gel run: separates DNA into bands. 3. Blot: transfer DNA from gel to nylon membrane. 4. Add probe: DNA complimentary to desired sequence labeled with DIG. 5. Add anti-DIG + AP, then substrate for chemiluminescence. 6. Expose to X-ray film, develop & print. Restriction Digestion for Southern Blot • Wild Type (Genomic) • PDI Plasmid PDI-2 • PDI Genomic Mutants: 1. 2A-1 1. 2A-1 1. 7A-1 2. 2A-2 2. 2A-2 2. 7B-1 3. 2B-2 3. 2B-2 • Restriction Enzymes: 3. 7B-2 EcoR1 HindIII EcoR1 Our Initial Gel* * Before dropping. Our Southern Blot Result Gel & Blot Comparisons Goals with Western Blot Using antibodies specific to Arabidopsis PDI proteins: • Detect PDI protein in wild type plants. • In mutant plants, determine the effect of the T-DNA insert on the expression of the PDI gene through movement or deletion of PDI protein band. Protein Separation 1. Protein extraction: liquid N, grinding, buffer. 2. Spectrophotometer protein concentration assay for standardization of well loading. 3. Protein separation with 2 SDS-PAGE gels. 4. Visualization of gel results: a) Coomassie stain of all proteins. b) Western blot to identify specific PDI proteins. Western Blot Process 1. Transfer proteins from PAGE to NC membrane. 2. Block with TBS and 5% nonfat milk. 3. React membrane with primary antibody to PDI-2 peptide (antibody made in rabbit). 4. Wash and react with secondary (donkey anti-rabbit) antibody conjugated to HRP. 5. Wash and react with substrate (luminol + enhancer.) Oxidized product results in light. 6. Light is detected with X-ray film. (Longer exposures appeared more effective.) Western Blot Nitrocellulose membrane Polyacrylamide Gel Our Coomassie stain result Our Western blot result Protein Gel Comparisons 2B 2A WT Western Blot Interpretation • Bands displayed on our blot are ambiguous. • We have 3 alternative explanations: a) All bands in all lanes are alternative forms of PDI-2. b) Anti-PDI peptide antibody from rabbit reacts with similar epitopes on unrelated proteins. c) 2° antibody from donkey reacts to similar epitopes on unrelated proteins.