| 1. | DNA digestion with enzymes |
| 2. | DNA extraction |
| 3. | Sample collection (blood, saliva, hair root etc.) |
| 4. | Probe hybridisation |
| 1. | Southern blotting |
| 2. | DNA extraction and purification |
| 3. | DNA denaturation |
| 4. | Gel electrophoresis |
| 1. | To make DNA fluorescent |
| 2. | To amplify DNA sequences |
| 3. | To prevent hybridisation with probes |
| 4. | To remove proteins and contaminants that interfere with enzyme action |
| 1. | They cut at random points, creating diversity |
| 2. | They amplify DNA |
| 3. | They cut at precise recognition sequences, ensuring reproducibility |
| 4. | They denature DNA for gel loading |
| 1. | It amplifies the DNA |
| 2. | It separates DAN fragments by size and charge |
| 3. | It fixes DNA permanently |
| 4. | It makes DNA visible without probes |
| I: | Gel fragments are unstable and difficult to probe |
| II: | Probes cannot bind in gel matrix III: Membrane provides a durable, flat surface |
| 1. | To bind to complementary VNTR sequences |
| 2. | To cut DNA further |
| 3. | To make DNA move faster in gel |
| 4. | To amplify VNTR regions |