Shanu Markand Biol142

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Across
  1. 3. Buffer to wash C elegans
  2. 4. Type of plate on which revertants grow
  3. 10. DNA in agarose gel move from positive end to this
  4. 11. Makes the sample heavier than buffer and visualize migration in gel
  5. 13. Technique by which DNA is amplified
  6. 14. binds to double stranded DNA and fluoresces under UV light
  7. 15. Buffer used for washing C albicans
  8. 16. name of the gene that we amplified by PCR denaturation Step 1 of PCR
  9. 17. our model organism for microbiome project
Down
  1. 1. amino acid important for survival of C albicans (discussed in lab)
  2. 2. This index can be used to measure species evenness.
  3. 5. Course director’s last name
  4. 6. short pair of DNA used in PCR that binds to template DNA
  5. 7. The number of copies of each chromosome in an organism’s genome
  6. 8. Enzyme used in PCR
  7. 9. Tube with lots of DNA fragments of certain sizes
  8. 12. Candida are mostly stable at this ploidy
  9. 14. Opportunistic pathogen species used in C elegans project