• 1 Preface
  • 2 Quartzy Requests and Inventory
    • 2.1 Quartzy Inventory
    • 2.2 Quartzy Requests
    • 2.3 Freezer Boxes
  • 3 Molecular: Best Practices
    • 3.1 Things to Consider
      • 3.1.1 Contamination
      • 3.1.2 Centrifugation
      • 3.1.3 Pipetting
    • 3.2 Preparing for an Experiment
      • 3.2.1 Reading
      • 3.2.2 Calculating
      • 3.2.3 Pre-Cleaning
    • 3.3 During the Experiment
      • 3.3.1 Testing
      • 3.3.2 Timing
      • 3.3.3 Writing
      • 3.3.4 Post-Cleaning
  • 4 Molecular: Sample Collection
    • 4.1 Sample Types
    • 4.2 DNA Isolation
    • 4.3 16S rRNA Isolation
    • 4.4 RNA Isolation
      • 4.4.1 Sample Conditions
      • 4.4.2 Tissue Processing with RNAlater
    • 4.5 Fibroblast Isolation
  • 5 Molecular: Isolation
    • 5.1 Leukocytes (Buffy Coat) Isolation
    • 5.2 Isolating DNA
    • 5.3 Isolating RNA
    • 5.4 Relevant Protocols
  • 6 Molecular: Genotyping
    • 6.1 Polymerase Chain Reaction (PCR)
      • 6.1.1 Primers
      • 6.1.2 Restriction Fragment Length Polymorphism (RFLP)
      • 6.1.3 Thermocycler
    • 6.2 Electrophoresis
      • 6.2.1 Analyzing Gels
    • 6.3 DNA Sequencing
    • 6.4 Relevant Protocols
  • 7 Molecular: Phenotyping
    • 7.1 Quantitative/Real-Time PCR
    • 7.2 RNA Sequencing
    • 7.3 Single-Cell RNA Sequencing
    • 7.4 16S rRNA Gene (DNA) Sequencing
    • 7.5 Relevant Protocols
  • 8 Molecular: Protocols
    • 8.1 Dilutions
      • 8.1.1 Stock vs Psuedo-stock vs Working Solutions
    • 8.2 Leukocytes (Buffy Coat) Isolation Protocol
      • 8.2.1 Further Washing and Platelet Removal (Optional)
    • 8.3 DNA Isolation Protocol
      • 8.3.1 DNA Isolation from Blood
      • 8.3.2 DNA Isolation from Blood Write-Up
      • 8.3.3 DNA Isolation from Solid Tissue Write-Up
    • 8.4 RNA Isolation Protocol
      • 8.4.1 RNase Free
      • 8.4.2 Kits
    • 8.5 Designing Primers
      • 8.5.1 Ordering Primers
      • 8.5.2 Stock Solution
      • 8.5.3 Working Solution
    • 8.6 PCR Protocol
      • 8.6.1 GoTaq Colorless Master Mix
      • 8.6.2 Restriction Fragment Length Polymorphism Analysis (Optional)
      • 8.6.3 Thermocycler
    • 8.7 Capillary Electrophoresis
      • 8.7.1 Organizing Data
      • 8.7.2 Syncing Data
    • 8.8 qPCR Protocol
      • 8.8.1 Materials
      • 8.8.2 Experiment Preparation
      • 8.8.3 Wet Chemistry
      • 8.8.4 LightCycler 96 Setup
  • 9 Appendix A: Troubleshooting
    • 9.1 PCR
    • 9.2 qPCR
  • 10 Appendix B: Scaling Tables
  • 11 Appendix C: Equipment and Manuals
  • 12 Appendix D: Kit Protocols
  • 13 Appendix E: Experiment Templates
  • 14 Appendix F: Safety Information
  • 15 Appendix G: Projects
  • 16 Appendix H: Vendors

Vallender Lab Protocol Manual

6.4 Relevant Protocols

  • PCR
    • Designing Primers
    • Troubleshooting PCR
    • Capillary Electrophoresis