Team:Washington/Primers

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Revision as of 21:00, 9 September 2011


EVERYONE PLEASE ENTER AND FILL OUT THE TABLE

For info on [http://en.wikipedia.org/wiki/Help:Table#Sorting Wiki Tables]


EXAMPLE TABLE (DO NOT MODIFY)

Sortable and collapsible table
Alphabetic Numeric Date Unsortable
d 20 2008-11-24 This
b 8 2004-03-01 column
a 6 1979-07-23 cannot
c 4.2 1492-12-08 be
e 0 1601-08-13 sorted.


TABLE TO BE FILLED OUT

LEGEND:

  • Template Part #: The Registry Number of the Part being amplified from
  • Template Form: The source form of the template DNA
    • Miniprep (M)
    • Colony (C)
    • PCR Product (P)
  • Template Source: Where the template is originally from, such as 2011 Parts Kits, Synthesized Gene, Genomic, etc
  • Forward Primer (5'->3'): Full sequence of the Forward primer used
  • Reverse Primer (5'->3'): Full sequence of the Reverse primer used
  • Annealing Temperature (Celsius): The annealing temperature used in the PCR reaction
  • Extension Time (seconds): The extension time used in the PCR reaction
  • Percent DMSO: Was DMSO added, if not 0, if so at what %
  • Polymerase Used: Which polymerase enzyme was used (e.g. Phusion, Taq, Vent, Pfu, etc)
  • Amplification Success (S, M, N): Was the amplification successful.
    • S = Single Band at Desired Size
    • M = Multiple Bands, but one at desired length
    • N = No band at desired length
  • Primer Name: The name of the primer ordered
  • Additional Notes: Any additional relevant information


Template Part # Template Form (M, C, P) Template Source Forward Primer (5'->3') Reverse Primer (5'->3') Annealing Temperature (Celsius) Extension Time (seconds) Percent DMSO Polymerase Used Amplification Success (S, M, N) Forward Primer Name Reverse Primer Name Additional Notes
TBD M Synthesized Gene GTTTCTTCGAATTCGCGGCCGCTTCTAGATGCCGCAGCTGGAA CCAATGCATTGGTTCTGCAGCGGCCGCTACTAGTATCAGTGGTGGTGGTG 60 30 0 Phusion S EX_Decarb_F RedDecarb_SP_2 Original reverse primer was missing extra nucleotides at end, so amplification worked, cloning didn't
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