BME100 f2013:Logistics: Difference between revisions

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'''TEMPLATE PAGES (SPRING 2013)'''
'''TEMPLATE PAGES (SPRING 2013)'''
* [[BME103_s2013:TEMPwu1 | Lab Write-up 1]]
* [[BME103_s2013:TEMPwu1 | DNA Lab Write-up 1]]
* [[BME103_s2013:TEMPwu2 | Lab Write-up 2]]
* [[BME103_s2013:TEMPwu2 | DNA Lab Write-up 2]]
* [[BME103_s2013:TEMPwu3 | Lab Write-up 3]]
* [[BME103_s2013:TEMPwu3 | DNA Lab Write-up 3]]
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Revision as of 10:43, 28 August 2013

BME 100 Fall 2013 Home
People
Lab Write-Up 1 | Lab Write-Up 2 | Lab Write-Up 3
Lab Write-Up 4 | Lab Write-Up 5 | Lab Write-Up 6
Course Logistics For Instructors
Photos
Wiki Editing Help


COURSE SPECS

  • ~180 Freshmen
    • 2 Lab sections, ~90 students per section
      • # groups, of ~5 students per group
  • 3 hours per class meeting


TEMPLATE PAGES (SPRING 2013)


MATERIALS & METHODS - DNA AMPLIFICATION

  • Reactions (100 μL total volume) contained:
    • Template DNA - Kozak (BBa_BBa_J176012) inserted in plasmid vector V0120 (BBa_J176127) via standard BioBrick ligation; ~10 ng per "positive" reaction; negative reactions contained no plasmid
    • Primers - Forward primer P0001 (5'-gggttttcccagtcacgacg), Reverse primer P0002 (5'-tgtggaattgtgagcggataaca). Amplicon size = 277 bp, spanning some of the vector, the BioBrick prefix sites, Kozak, the BioBrick suffix, and more vector sequence.
    • 2x GoTaq colorless PCR Master Mix - Promega M7133
  • A few of the samples were checked via standard ethidium bromide-stained agarose gel electrophoresis outside of class (see [1]). All other samples were measured via SYBRgreen staining on an LED fluorimeter.
  • All reactions were run on an Open PCR machine.


MATERIALS & METHODS - DNA IMAGING

  • Details to be added soon


OBTAINING MATERIALS

  • We have written several worksheets and hand outs for this course.
  • Please contact one of the instructors if you are interested in obtaining copies.