Team:KAIT Japan/Notebook

From 2014.igem.org

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:<big>'''Date:9/29'''</big> The vector and the insert were NANOSEP and lectrophoresis
:<big>'''Date:9/29'''</big> The vector and the insert were NANOSEP and lectrophoresis
:<big>'''Date:9/30'''</big> The vector and the insert were ligation and transformation
:<big>'''Date:9/30'''</big> The vector and the insert were ligation and transformation
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:<big>'''Date:10/1'''</big>  
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:<big>'''Date:9/30'''</big> The GFP+HlyA was PCR and DNA purify
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:<big>'''Date:10/2'''</big>
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:<big>'''Date:10/1'''</big> Electrophoresis the GFP+HlyA was PCR and DNA purify in 9/30
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:<big>'''Date:10/3'''</big>
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:<big>'''Date:10/2'''</big> Restriction enzyme treatment and ligation the GFP+HlyA
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:<big>'''Date:10/4'''</big>
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:<big>'''Date:10/3'''</big> Check the ligation in 10/2
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:<big>'''Date:10/4'''</big>  
:<big>'''Date:10/5'''</big>
:<big>'''Date:10/5'''</big>
:<big>'''Date:10/6'''</big>
:<big>'''Date:10/6'''</big>

Revision as of 09:50, 16 October 2014

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KAIT Japan2013 Kanako.png

KAIT Japan 2014 iGEMRogo.png
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Home

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Team

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Project

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Parts

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Protocol

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Notebook

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Results

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Safety

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Human Practice


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 Electrophoresis the ligation the GFP+HlyA in 9/18
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 Restriction enzyme treatment the GFP+HlyA and the pSBIC3
Date:9/29 The vector and the insert were NANOSEP and lectrophoresis
Date:9/30 The vector and the insert were ligation and transformation
Date:9/30 The GFP+HlyA was PCR and DNA purify
Date:10/1 Electrophoresis the GFP+HlyA was PCR and DNA purify in 9/30
Date:10/2 Restriction enzyme treatment and ligation the GFP+HlyA
Date:10/3 Check the ligation in 10/2
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 PCR
Date:9/4 Transformation
Date:9/5 Colony PCR
Date:9/7 ColonyPCR
Date:9/8 DNA extraction and Sequence(to To confirm whether variation happened in DNA of IL-10β)
Date:9/9 DNA sequence
Date:9/10 PCR and Electtrophoresis
Date:9/11 Colony PCR
Date:9/12 DNA extraction
Date:9/13 PCR and Electrophoresis
Date:9/15 ultrafiltration
Date:9/16 DNA sequence(to comfirm whether variation happened in DNA of IL-10β)
Date:9/20 PCR
Date:9/23 Colony PCR
Date:9/24 Electrophoresis
Date:9/26 ultrafiltration
Date:9/27 PCR and colony PCR
Date:9/29 Electrophoresis
Date:9/30 DNA Extraction
Date:10/1 Colony PCR and DNA extraction
Date:10/2 Electrophoresis
Date:10/3 PCR(using Prime Star MAX Premix) and Electrophoresis
Date:10/4 PCR(using Prime Star MAX Premix) and Electrophoresis
Date:10/5 Electrophoresis



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