From 2014.igem.org
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| :<big>'''Date:9/23'''</big> PCR and DNA purify | | :<big>'''Date:9/23'''</big> PCR and DNA purify |
| :<big>'''Date:9/24'''</big> TA Cloning was GFP and HlyA | | :<big>'''Date:9/24'''</big> TA Cloning was GFP and HlyA |
- | :<big>'''Date:9/25'''</big> | + | :<big>'''Date:9/26'''</big> Restriction enzyme treatment the ligation the GFP+HlyA in 9/22 |
- | :<big>'''Date:9/26'''</big>
| + | :<big>'''Date:9/27'''</big> Check the TA cloning of GFP+HlyA |
- | :<big>'''Date:9/27'''</big> | + | |
- | :<big>'''Date:9/28'''</big>
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| :<big>'''Date:9/29'''</big> | | :<big>'''Date:9/29'''</big> |
| :<big>'''Date:9/30'''</big> | | :<big>'''Date:9/30'''</big> |
Revision as of 09:32, 16 October 2014
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Notebook
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Notebook
- We made an experiment every day. It was process at trial and error.
Creating parts of HlyA and GFP
- Date:8/22 The refinement of DNA and PCR and Electrophoresis
- Date:8/25 PCR and Electrophoresis and Restriction
- Date:8/26 Insert gene into TAvectar and Transformation
- Date:8/26 Blue white Selection and Electrophoresis(8/25 Restriction) and DNA Extraction
- Date:8/27 Electrophoresed the DNA that We did refinement on August 26 to confirmed it
- Date:8/28 Check the HlyA and GFP for colony PCR
- Date:8/29 DNA purify the HlyA and GFP
- Date:8/29 Ligation product and check for PCR
- Date:9/1 Build replica the HlyA and GFP
- Date:9/1 Restriction enzyme treatment the HlyA and GFP
- Date:9/2 Restriction enzyme treatment the HlyA and GFP in 9/1 was NANOSEP
- Date:9/3 Ligation and PCR, DNA purification the HlyA and GFP
- Date:9/4 Restriction enzyme treatment the HlyA and GFP
- Date:9/5 Restriction enzyme treatment the vector
- Date:9/5 Ligation the vector and insert. So transformation.
- Date:9/9 Check the HiyA and GFP replica.Ligation and Transformation the vector and insert DNA.
- Date:9/10 Transformation in 9/9 check the colony PCR.TA cloning the HlyA+GFP.
- Date:9/11 Ligation the vector and insert DNA.
- Date:9/12~9/15 Transformation the Ligation product.
- Date:9/16 Noticed wrong the primer.so restart from the First.
- Date:9/17 PCR the DNA abstracted for iGEM kit.It was TA cloning and restriction enzyme treatment.
- Date:9/18 Ligation the GFP and HlyA.
- Date:9/19 Ligation the GFP+HlyA in 9/18 was Electrophoresis
- Date:9/20 DNA purify and PCR
- Date:9/21 PCR and DNA purify
- Date:9/22 Ligation the GFP+HlyA
- Date:9/23 PCR and DNA purify
- Date:9/24 TA Cloning was GFP and HlyA
- Date:9/26 Restriction enzyme treatment the ligation the GFP+HlyA in 9/22
- Date:9/27 Check the TA cloning of GFP+HlyA
- Date:9/29
- Date:9/30
- Date:10/1
- Date:10/2
- Date:10/3
- Date:10/4
- Date:10/5
- Date:10/6
Creating parts of STAT3
- Date:8/19 PCR(8/18 Miniprep) and Electrophoresis
- Date:8/20~8/22 PCR(Lowered 2℃ from Tm value.) and Electrophoresis
- Date:8/25 PCR and Electrophoresis(Changed to Taq HOTSTER from EX taq.)
- Date:8/26 PCR and Electrophoresis(Using a mutation primer.)
- Date:8/27 First Variation introduction (with Prime STAR Max)
- Date:9/2 PCR and Electrophoresis
- Date:9/5~9/8 PCR and Electrophoresis
- Date:9/9 Sequence(to To confirm whether variation happened in DNA of STAT3 )
- Date:9/10~9/12 PCR and Electrophoresis
- Date:9/13~9/15 DNA purification and electrophoresis
- Date:9/16~9/17 DNA purification and colony PCR(Failure)
- Date:9/18 colony PCR(Failure)
- Date:9/19~9/22 colony PCR and electrophoresis
- Date:9/23 PCR and Electrophoresis(We found out that DNA polymerase was malfunction)
- Date:9/24 PCR and Electrophoresis and DNA DNA purification
- Date:9/25 PCR(to find annealing temperature)
- Date:9/26~9/30 DNA purification and electrophoresis(to use DNA for the sequence)
- Date:10/1 Dilution after Concentration measurement of DNA
- Date:10/2 Sequence(to check mutation of DNA)/The variation was not found.
- Date:10/4 PCR and electrophoresis
- Date:10/5~10/7 Colony PCR and DNA purification
- Date:10/8 Concentration measurement of DNA
- Date:10/9 Sequence(to check mutation of DNA)/The variation was not found
Creating parts of IL-10α,IL-10β
- Date:8/19 PCR(8/18 Miniprep) and Electrophoresis
- Date:8/20~8/22 PCR(Lowered 2℃ from Tm value.) and Electrophoresis
- Date:8/25 PCR and Electrophoresis(Changed to Taq HOTSTER from EX taq.)
- Date:8/26 PCR and Electrophoresis(Using a mutation primer.)
- Date:8/27 First Variation introduction (with Prime STAR Max)
- Date:9/2
- Date:9/4
- Date:9/5
- Date:9/7
- Date:9/8
- Date:9/9
- Date:9/10
- Date:9/11
- Date:9/12
- Date:9/13
- Date:9/15
- Date:9/20
- Date:9/23
- Date:9/24
- Date:9/26
- Date:9/27
- Date:9/29
- Date:9/30
- Date:10/1
- Date:10/2
- Date:10/3
- Date:10/4
- Date:10/5
- Date:9/8 Sequence(to To confirm whether variation happened in DNA of IL-10α,IL-10β)
- Date:9/10-10/9 Sequence preparation & Sequence
Creating parts of HRV,IL-5Ra,IL-5Rb,AraC,Arac Promoter
- Date:9/16
- Date:9/17
- Date:9/18
- Date:9/19
- Date:9/20
- Date:9/21
- Date:9/22
- Date:9/23
- Date:9/24
- Date:9/25
- Date:9/26
- Date:9/27
- Date:9/28
- Date:9/29
- Date:9/30
- Date:10/1
- Date:10/2
- Date:10/3
- Date:10/4
- Date:10/5
- Date:10/6
- Date:10/7
- Date:10/8
- Date:10/9
- Date:10/10
- Date:10/11
- Date:10/12
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