IGEM:Harvard/2009/Notebook/Harvard iGEM 2010/2010/06/18: Difference between revisions

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'''Progress'''  
'''Progress'''  
# Identified allergens in arabidopsis, strawberries,tomatoes, and carrots and created primers for amplifying out these allergens [http://openwetware.org/wiki/IGEM:Harvard/2010/Team_Allergy| (see primers and sequences)]  
# Identified allergens in arabidopsis, strawberries,tomatoes, and carrots and created primers for amplifying out these allergens [http://openwetware.org/wiki/IGEM:Harvard/2010/Team_Allergy| (see primers and sequences)]  
# Extracted cDNA from strawberries and tried to PCR out our strawberry allergen (Fra a 1), but were uanble to do so
# Extracted cDNA from strawberries and tried to PCR out our strawberry allergen (Fra a 1), but were unble ato do so
# Looked to find introns ~ 800 bp to use to create our hairpins since it was difficult to acquire pHannibal vector w/ the pdk intron
# Looked to find introns ~ 800 bp to use to create our hairpins since it was difficult to acquire pHannibal vector w/ the pdk intron


'''Future Directions'''
'''Future Directions'''


# Look towards ordering amiRNA for silencing
# Look towards ordering [[Media:Aimrna.pdf|amiRNA]]for silencing
# Waiting on arabidopsis plants to grow to extract genomic DNA (mon)
# Waiting on arabidopsis plants to grow to extract genomic DNA (mon)
# Look to find introns to use in creation of hairpin DNA  
# Look to find introns to use in creation of hairpin DNA  

Revision as of 12:01, 18 June 2010

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Week 1 Summary (6/18/2010)

Team Vector

Team Flavor

Team Allergy

Progress

  1. Identified allergens in arabidopsis, strawberries,tomatoes, and carrots and created primers for amplifying out these allergens (see primers and sequences)
  2. Extracted cDNA from strawberries and tried to PCR out our strawberry allergen (Fra a 1), but were unble ato do so
  3. Looked to find introns ~ 800 bp to use to create our hairpins since it was difficult to acquire pHannibal vector w/ the pdk intron

Future Directions

  1. Look towards ordering amiRNAfor silencing
  2. Waiting on arabidopsis plants to grow to extract genomic DNA (mon)
  3. Look to find introns to use in creation of hairpin DNA
  4. Cloning (digesting/ligating our sense/antisense/intron sequences necessary for hairpin creation into one vector to create biobricks)

Team Fence


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