Team:Kyoto/Notebook

From 2010.igem.org

(Difference between revisions)
(Tuesday, July 20)
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*Category: Transformation, PCR, Lysis Cassette
*Category: Transformation, PCR, Lysis Cassette
|-
|-
-
|Cultured plates in which colonies was observed at 37℃ from 07/21 20:50 to 07/22 17:00.
+
|(1) Cultured plates in which colonies was observed at 37℃ from 07/21 20:50 to 07/22 17:00.
|-
|-
-
|Made a master plate of the above plates.
+
|(2) Made a master plate of the above plates.
|-
|-
-
|Retried Transformation of iGEM Parts.
+
|(3) Retried [[Team:Kyoto/Protocols#Transformation|Transformation]] of iGEM Parts.
{| class="experiments"
{| class="experiments"
|Name||Well<sup>*1</sup>||Sample (µl)||Competent Cells (µl)||Total (µl)||Plate||Incubation||Result
|Name||Well<sup>*1</sup>||Sample (µl)||Competent Cells (µl)||Total (µl)||Plate||Incubation||Result
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* *1 "1-5-G" means well 5G in [http://partsregistry.org/Help:Spring_2010_DNA_distribution Spring 2010 DNA Distribution Kit] Plate 1.
* *1 "1-5-G" means well 5G in [http://partsregistry.org/Help:Spring_2010_DNA_distribution Spring 2010 DNA Distribution Kit] Plate 1.
|-
|-
-
|PCR PCR for S-R-Rz/Rz1 and S
+
|(4) [[Team:Kyoto/Protocols#PCR|PCR]] for S-R-Rz/Rz1 and S
* Dilute &lambda;DNA (0.5µg/µl) 100 times with MilliQ. The final concentration of template &lambda;DNA was 5ng/µl.
* Dilute &lambda;DNA (0.5µg/µl) 100 times with MilliQ. The final concentration of template &lambda;DNA was 5ng/µl.
{| class="experiments"
{| class="experiments"
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*Category: Lysis Cassette, parts
*Category: Lysis Cassette, parts
|-
|-
-
|1. Electrophoresis of the PCR products for 40min.
+
|(1) Electrophoresis of the PCR products for 40min.
[[Image:KyotoExp100722-1.png|right]]
[[Image:KyotoExp100722-1.png|right]]
* '''Discussion'''
* '''Discussion'''
* Length of S and S-R-Rz/Rz1 is 370bp, 1300bp, so PCR succeeded.
* Length of S and S-R-Rz/Rz1 is 370bp, 1300bp, so PCR succeeded.
|-
|-
-
|2. [[Team:Kyoto/Protocols#Miniprep|Miniprep]] of iGEM Parts.
+
|(2) [[Team:Kyoto/Protocols#Miniprep|Miniprep]] of iGEM Parts.
{| class="experiments"
{| class="experiments"
!Name||Concentration(ng/&micro;l)
!Name||Concentration(ng/&micro;l)
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* The concentration of all samples was very week. Probably our shaking incubation was week.
* The concentration of all samples was very week. Probably our shaking incubation was week.
|-
|-
-
|3. Culture plates and make master plates of <partinfo>pSB4K5</partinfo> and <partinfo>B0015</partinfo> from 7/22 17:00 to 7/23 10:00.
+
|(3) Culture plates and make master plates of <partinfo>pSB4K5</partinfo> and <partinfo>B0015</partinfo> from 7/22 17:00 to 7/23 10:00.
|}
|}
----
----
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* Category:  
* Category:  
|-
|-
-
|1. [[Team:Kyoto/Protocols#Miniprep|Miniprep]] of iGEM Parts.
+
|(1) [[Team:Kyoto/Protocols#Miniprep|Miniprep]] of iGEM Parts.
{| class="experiments"
{| class="experiments"
!Name||Concentration(ng/&micro;l)
!Name||Concentration(ng/&micro;l)
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* The concentration of <partinfo>pSB4K5</partinfo> is high, so this condition of shaking incubation is moderate.
* The concentration of <partinfo>pSB4K5</partinfo> is high, so this condition of shaking incubation is moderate.
|-
|-
-
|2. Picked up 1, 3, 5, 7 of the products of PCR, and purified by PCR-purification.
+
|(2) Picked up 1, 3, 5, 7 of the products of PCR, and purified by PCR-purification.
{| class="experiments"
{| class="experiments"
!Sample||Concentration (ng/&micro;l)||New Name||
!Sample||Concentration (ng/&micro;l)||New Name||
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* The concentration of sample number 1 and 5, the PCR products of S-R-Rz, is week, so we desided to retry PCR.
* The concentration of sample number 1 and 5, the PCR products of S-R-Rz, is week, so we desided to retry PCR.
|-
|-
-
|3. Retry of PCR of S-R-Rz/Rz1.
+
|(3) Retry of PCR of S-R-Rz/Rz1.
{| class="experiments"
{| class="experiments"
!Sample||Water||25mM MgSO4||2mM dNTPs||10×Buffer for KOD plus ver.2||Template DNA (5ng/&micro;l)||Primer S-R-Rz/Rz1 Forward (10&micro;M)||Primer S-R-Rz/Rz1 Reverse (10&micro;M)||KOD plus ver.2||Total
!Sample||Water||25mM MgSO4||2mM dNTPs||10×Buffer for KOD plus ver.2||Template DNA (5ng/&micro;l)||Primer S-R-Rz/Rz1 Forward (10&micro;M)||Primer S-R-Rz/Rz1 Reverse (10&micro;M)||KOD plus ver.2||Total
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* PCR condition : 94&#x2103; x 2min, (98&#x2103; x 10sec, 55&#x2103; x 30sec, 68&#x2103; x 1min) x 30cycles, 4&#x2103; forever.
* PCR condition : 94&#x2103; x 2min, (98&#x2103; x 10sec, 55&#x2103; x 30sec, 68&#x2103; x 1min) x 30cycles, 4&#x2103; forever.
|-
|-
-
|4. Digested <partinfo>J06702</partinfo> by EcoRI, XbaI, SpeI, PstI to check function of our Restriction enzymes.
+
|(4) Digested <partinfo>J06702</partinfo> by EcoRI, XbaI, SpeI, PstI to check function of our Restriction enzymes.
{| class="experiments"
{| class="experiments"
!Sample||10xBuffer||BSA||Enzyme||MilliQ||Total||Incubation
!Sample||10xBuffer||BSA||Enzyme||MilliQ||Total||Incubation
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|}
|}
|-
|-
-
|5. Electrophoresis of above sample for 35min.
+
|(5) Electrophoresis of above sample for 35min.
[[Image:KyotoExp100723-1.png|right]]
[[Image:KyotoExp100723-1.png|right]]
* '''Discussion'''
* '''Discussion'''
* Comparison to sample 5(control, circular DNA), the bands of sample 1, 2, 3, 4 was shifted. The DNA of sample 1, 2, 3, 4 was linearized by Restriction enzymes.  So, our restriction enzymes work correctly.
* Comparison to sample 5(control, circular DNA), the bands of sample 1, 2, 3, 4 was shifted. The DNA of sample 1, 2, 3, 4 was linearized by Restriction enzymes.  So, our restriction enzymes work correctly.
|-
|-
-
|6. To insert S gene to GFP, we digested the PCR products of S gene by EcoRi and SpeI, and GFP by EcoRl and XbaI.
+
|(6) To insert S gene to GFP, we digested the PCR products of S gene by EcoRi and SpeI, and GFP by EcoRl and XbaI.
{| class="experiments"
{| class="experiments"
!Sample||10×Buffer||Enzyme 1||Enzyme 2||MilliQ||Total||Incubation
!Sample||10×Buffer||Enzyme 1||Enzyme 2||MilliQ||Total||Incubation

Revision as of 16:27, 27 August 2010

Contents

Index

Notebook

Tuesday, July 20
  • By: Wataru, Tomo, Yuki, Kazuya, Ken, Makoto
  • Category: Antibiotic, Transformation
(1) Solubilized of antibiotics, Ampicillin and Kanamycin as the following.
  • 1. Mix the following (final concentration is 50mg/ml).
    • For Ampicillin: 1g Ampicillin and 20ml MilliQ.
    • For Kanamycin: 0.5g Kanamycin and 10ml MilliQ.
  • 2. Dispense 1.1ml of the mixture into 1.5ml tubes.
  • 3. Store in the freezer (-20℃).
(2) Made plates for LB (Ampicillin+) and LB (Kanamycin+).
(3) Transformed iGEM Parts.
NameWell*1Sample (µl)Competent Cells (µl)Total (µl)PlateIncubationResult
<partinfo>J23100</partinfo>1-18-C12021LB (Ampicillin+)At 37℃ 7/20 20:50 - 7/21 17:00○
<partinfo>J23105</partinfo>1-18-M12021○
<partinfo>J23116</partinfo>1-20-M12021○
<partinfo>R0011</partinfo>1-6-G12021○
<partinfo>E0840</partinfo>1-12-O12021○
<partinfo>J06702</partinfo>2-8-E12021○
<partinfo>pSB4K5</partinfo>1-5-G12021×
<partinfo>B0015</partinfo>1-23-L12021LB (Kanamycin+)×
  • *1 "1-18-C" means well 18C in [http://partsregistry.org/Help:Spring_2010_DNA_distribution Spring 2010 DNA Distribution Kit] Plate 1.
  • Discussion
  • A vector of "pSB4K5" is Kanamycin-resistance, however, we plated it to LB plate (Ampicillin+).
  • And We didn't pre-culture "B0015" despite its vector is Kanamycin-resistance.
  • So, it was predicted that we will fail the transformation of "pSB4K5" and "B0015".

Wednesday, July 21
  • By: Wataru, Ken, Makoto, Takuya Yamamoto
  • Category: Transformation, PCR, Lysis Cassette
(1) Cultured plates in which colonies was observed at 37℃ from 07/21 20:50 to 07/22 17:00.
(2) Made a master plate of the above plates.
(3) Retried Transformation of iGEM Parts.
NameWell*1Sample (µl)Competent Cells (µl)Total (µl)PlateIncubationResult
<partinfo>pSB4K5</partinfo>1-5-G12021LB (Kanamycin+)At 37℃ 7/21 20:50 - 7/22 16:30○
<partinfo>B0015</partinfo>1-23-L12021○
  • *1 "1-5-G" means well 5G in [http://partsregistry.org/Help:Spring_2010_DNA_distribution Spring 2010 DNA Distribution Kit] Plate 1.
(4) PCR for S-R-Rz/Rz1 and S
  • Dilute λDNA (0.5µg/µl) 100 times with MilliQ. The final concentration of template λDNA was 5ng/µl.
No.Water25mM MgSO42mM dNTPs10xBuffer for KOD Plus ver.2TemplateDNA (5ng/µl)Primer S-R-Rz/Rz1 Forward (10µM)Primer S-R-Rz/Rz1 Reverse (10µM)Primer S Reverse (10µM)KOD Plus ver.2Total
128µl3µl5µl5µl5µl1.5µl1.5µl-1µl50µl
228µl3µl5µl5µl5µl1.5µl1.5µl-1µl50µl
328µl3µl5µl5µl5µl1.5µl-1.5µl1µl50µl
428µl3µl5µl5µl5µl1.5µl-1.5µl1µl50µl
528µl3µl5µl5µl5µl1.5µl1.5µl-1µl50µl
628µl3µl5µl5µl5µl1.5µl1.5µl-1µl50µl
728µl3µl5µl5µl5µl1.5µl-1.5µl1µl50µl
828µl3µl5µl5µl5µl1.5µl-1.5µl1µl50µl
  • Forward Primer of S-R-Rz/Rz1 and S is common.
  • PCR condition : 94℃ x 2min, (98℃ x 10sec, 55℃ x 30sec, 68℃ x 1min) x 30cycles, 4℃ forever.

Thursday 22, July
  • By: Wataru
  • Category: Lysis Cassette, parts
(1) Electrophoresis of the PCR products for 40min.
KyotoExp100722-1.png
  • Discussion
  • Length of S and S-R-Rz/Rz1 is 370bp, 1300bp, so PCR succeeded.
(2) Miniprep of iGEM Parts.
NameConcentration(ng/µl)
<partinfo>J23100</partinfo>18.5
<partinfo>J23105</partinfo>12.5
<partinfo>J23116</partinfo>14.6
<partinfo>R0011</partinfo>8.6
<partinfo>E0840</partinfo>12.1
<partinfo>J06702</partinfo>14.7
  • Discussion
  • The concentration of all samples was very week. Probably our shaking incubation was week.
(3) Culture plates and make master plates of <partinfo>pSB4K5</partinfo> and <partinfo>B0015</partinfo> from 7/22 17:00 to 7/23 10:00.

Friday 23, July
  • By: Wataru, Tomo, Makoto
  • Category:
(1) Miniprep of iGEM Parts.
NameConcentration(ng/µl)
<partinfo>pSB4K5</partinfo>79.2
<partinfo>B0015</partinfo>-
  • Discussion
  • We lost <partinfo>B0015</partinfo> by our mistake.
  • The concentration of <partinfo>pSB4K5</partinfo> is high, so this condition of shaking incubation is moderate.
(2) Picked up 1, 3, 5, 7 of the products of PCR, and purified by PCR-purification.
SampleConcentration (ng/µl)New Name
118.6-
377.6S-1
533.6-
765.4S-2
  • Discussion
  • The concentration of sample number 1 and 5, the PCR products of S-R-Rz, is week, so we desided to retry PCR.
(3) Retry of PCR of S-R-Rz/Rz1.
SampleWater25mM MgSO42mM dNTPs10×Buffer for KOD plus ver.2Template DNA (5ng/µl)Primer S-R-Rz/Rz1 Forward (10µM)Primer S-R-Rz/Rz1 Reverse (10µM)KOD plus ver.2Total
3a28µl3µl5µl5µl5µl1.5µl1.5µl1µl50µl
3b2835551.51.5150
4.5a26.54.55551.51.5150
4.5b26.54.55551.51.5150
6a2565551.51.5150
6b2565551.51.5150
  • PCR condition : 94℃ x 2min, (98℃ x 10sec, 55℃ x 30sec, 68℃ x 1min) x 30cycles, 4℃ forever.
(4) Digested <partinfo>J06702</partinfo> by EcoRI, XbaI, SpeI, PstI to check function of our Restriction enzymes.
Sample10xBufferBSAEnzymeMilliQTotalIncubation
15µl1EcoRI 0.13.610At 37℃ 7/23 18:00 - 7/23 18:30
251XbaI 0.13.610
351SpeI 0.13.610
451PstI 0.13.610
551-3.710
(5) Electrophoresis of above sample for 35min.
KyotoExp100723-1.png
  • Discussion
  • Comparison to sample 5(control, circular DNA), the bands of sample 1, 2, 3, 4 was shifted. The DNA of sample 1, 2, 3, 4 was linearized by Restriction enzymes. So, our restriction enzymes work correctly.
(6) To insert S gene to GFP, we digested the PCR products of S gene by EcoRi and SpeI, and GFP by EcoRl and XbaI.
Sample10×BufferEnzyme 1Enzyme 2MilliQTotalIncubation
S-111µl5EcoRI 0.2SpeI 0.233.650At 37℃ for 2h
S-2115EcoRI 0.2SpeI 0.233.650
<partinfo>E0840</partinfo>(GFP)455EcoRI 0.2XbaI 0.2050
  • After PCR purification, evaporated them and diluted 3ul.
Ligated over night
SampleVectorInsertLigation HighTotal
S-GFP-1<partinfo>E0840</partinfo> 0.5µlS-1 0.512
S-GFP-2<partinfo>E0840</partinfo> 0.5S-2 0.512
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