BME100 f2013:Logistics: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
No edit summary
No edit summary
Line 25: Line 25:
* [[BME103_f2013:TEMPwu4 | DNA Lab Write-up 4]]
* [[BME103_f2013:TEMPwu4 | DNA Lab Write-up 4]]
* [[BME100_f2013:TEMPwu5 | DNA Lab Write-up 5]]
* [[BME100_f2013:TEMPwu5 | DNA Lab Write-up 5]]
* [[BME100_f2013:TEMPwu6 | DNA Lab Write-up 6]]
<br>
<br>



Revision as of 16:30, 20 November 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)

TEMPLATE PAGES (FALL 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.