Team:Peking/Notebook/MJing

From 2010.igem.org

(Difference between revisions)

Latest revision as of 10:12, 27 October 2010

Students and Instructors

NOTEBOOK HOME

CountDown

Vistors From...

Jing Miao's Notes

I designed to engineer this operon under the regulation of T7 promoter, which is regulated by upstream T7 polymerase, to fulfill the goal that the absorbance of Hg(II) will be enhanced for an efficient bioabsorbent. Also I cloned and assembled agn43 into the inductive aggregation module. Agn43 is drove by PO promoter, which is the terminal of a cascade amplification

download his notes

July

[TOP]

7.3

Antigen 43 PCR, 20ul system. T3 polymerase PCR.

Identify them by 1% agarose gel electrophoresis.

7.4

Antigen 43 PCR using different annealing temperature, with gradient 1 ℃.

Attend the group seminar.

Retrieve the PCR product of T3 polymerase and digest it with EcoRI and PstI. Digest for the whole night.

7.5

Identify the product by agarose gel electrophoresis. Retrieve the PCR product of Antigen 43.

Retrieve the digested T3 polymerase and ligated it to the plasmid PSB1A2.

Transform the plasmid to Trans 5α strain.

PCR the antigen 43 with much larger annealing temperature gradient. Identify it with electrophoresis.

7.6

Design the primer of antigen 43 again by Primer Premier 5.0.

7.8

PCR antigen 43 using nest-PCR procedure. Using Taq DNA polymerase to do the first step nest PCR.

Identify it by electrophoresis. Retrieve the 3k band and do the second step of nest PCR by using the product of the first step as template.

7.9

Identify the second PCR product by electrophoresis. Retrieve the 3k band and digest it with EcoRI and SpeI to put it into plasmid. Digest it with PstI to test whether this is antigen 43.( antigen 43 have 6 PstI digestion sites.)

Design the six point mutation primer.

7.10

Do the transformation and ligation.

7.12

Prepare plasmid DNA.

Digest the plasmid DNA with PstI to identify it.

PCR the product using Easytaq DNA polymerase to identify the molecule weight of the product.

7.13

Learn to do the western blotting. Write the protocols.

Digest merT, merP and merC with Xbal and PstI. Meanwhile digest B0034(RBS) with SpeI and PstI.

Connect the two digested product together.

Transform the ligation product into Trans5αstrain.

Pick the single clone from the plate.

Send the PCR product of Antigen 43 for sequencing.

7.14

Prepare the plasmid DNA of rbs+merT, rbs+merP, rbs+merC.

Do the western blotting.

7.15

Digest the plasmid DNA by EcoRI and PstI to identify it.

Digest rbs+merT with Spel and Pstl and digest rbs+merP with Xbal and Pstl.

Identify them using agarose gel electrophoresis.

7.16

Connect rbs with merT, merP and merC again.

Do the first point mutation. First PCR the antigen 43 gene with designed point mutation primers, then retrieve it by electrophoresis. Then do the blunting kination, finally do the ligation and put it into strains by transformation.

7.18

Prepare the plasmid DNA for rbs+merT, rbs+merP and rbs+merC, Antigen 43 mutant 1.

Identify them using electrophoresis.

Connect rbs+merT with rbs+merP.

Do the second step of point mutation for antigen 43. Do the PCR step. Identify it by electrophoresis. Blunting kination, ligation and transformation.

Send the first point mutation product for sequencing.

The rbs+merT,rbs+merP and rbs+merC sequenced correct.

7.19

Retrieve the product of digested rbs+merT and rbs+merP by electrophoresis. Connect the rbs+merT with rbs+merP,. Do the transformation.

Pick the single clone of antigen 43 second step point mutation strain.

7.20

Prepare the plasmid DNA of antigen 43 second point mutation strain. Send it for sequencing.

Do the third step point mutation.

Identify the plasmid DNA by electrophoresis. Retrieve the third point mutation PCR product by electrophoresis.

Digest rbs+merT+rbs+merP with Spel and Pstl, digest rbs+merC with Xbal and Pstl.

7.21

Identify the product of the digestion using electrophoresis.

Pick the single clone of the 3rd point mutation of antigen 43 strain on the plate.

7.22

Connect rbs+merT+rbs+merP with rbs+merC.

Using easyPFu to PCR antigen 43.The forward primer contains a rbs. Digest it with EcoRl and Spel to put it into PSB1A2 plasmid.

Prepare the plasmid DNA of the product of the third point mutation of antigen 43.digest it with EcoRl and SpeI to identify it.

Do the 4th point mutation PCR step.

7.23

Identify the plasmid using agarose gel electrophoresis.

Send the plasmid DNA for sequencing.

Put the rbs+agn43 into plasmid by ligation.

7.29

Attend the group seminar.

Prepare the plasmid DNA for rbs+merT+rbs+merP+rbs+merC. Digest it with EcoRl and Pstl for identification. Digest it with Xbal and Pstl and digest the plasmid contains T7 promoter with Spel and Pstl.

Do the 5th point mutation of antigen 43. Do the PCR step.

Identify the product of the 4th point mutation and the rbs+merT+rbs+merP+rbs+merC by electrophoresis. Collect those correct ones and send them for sequencing.

See the point mutation result in the sequence.

Identify the T7+rbs+merT+rbs+merP+rbs+merC by electrophoresis.

7.30

Digest rbs+agn43 with EcoRl and Xbal. Digest phiR73+Po promoter with EcoRl and Spel.

Retrieve the digested T7+rbs+merT+rbs+merP+rbs+merC gel.

Do the transformation.

7.31

Digest 2-2E constitutive promoter with EcoRl and Spel. Digest rbs+agn43 with EcoRl and Xbal.

Connect 2-2E promoter with rbs+agn43.

August

[TOP]

8.1

Prepare the plasmid DNA of T7+rbs+merT+rbs+merP+rbs+merC and PhiR73+Po promoter+rbs+antigen 43.

Prepare the plasmid DNA of 2-2E promoter+rbs+antigen 43.

Identify PhiR73+Po promoter+rbs+antigen 43 and 2-2E promoter+rbs+antigen 43 using electrophoresis.

8.2

Send the correct ones for sequencing.

Digest rbs+antigen 43 again.

8.4

Pick the clone of PhiR73+Po promoter+rbs+antigen 43 on the plate for autoaggregation assay.

Plan the assay.

Design new primers for antigen 43 which contains different promoters in the forward primer.

8.5

Preliminary autoaggregation assay.

Send PhiR73+Po promoter+rbs+antigen 43 for sequencing.

Transform PhiR73+Po promoter+rbs+antigen 43 into BL21 strains.

8.6

Pick the single clone.

Induce the antigen 43 gene’s expression by adding 10^-5 M IPTG for 4 hours.

Do the auto-aggregation assay( for detail, see the inductive aggregation page or antigen 43 part.)

PCR the rbs+agn43 using easyPFU.

Identify it using electrophoresis.

Digest the PCR product using EcoRl and Spel to put it into PSB1A2.

Do the ligation and transformation.

Send some of the PCR product for sequencing.

8.7

Digest merT+merC with Spel and Pstl, digest merP with Xbal and Pstl.

Retrieve the gel. Do the ligation.

Pick three clones of rbs+merP.

8.8

Prepare the plasmid DNA for rbs+merP and merT+merC.

Pick single clones of merT+merP+merC. Do the colony PCR.

Retrieve the rbs+agn43.

Do the ligation and transformation.

8.9

PCR antigen 43.

Nest PCR using nest primers. Do the first step.identify it using electrophoresis.

8.10

PCR antigen 43 using nest primers. Using different template.

Using better template to run PCR.

Do the transformation of antigen 43.

8.11

Retrieve the product of rbs+agn43. Digest it and do the ligation and transformation.

8.12

Pick the single clone of rbs+agn43.

Digest 1-23L with EcoRl and Xbal. Digest T7+merT+merP+merC with EcoRl and Spel.

Digest pmerT+GFP with Spel and Pstl, digest TPC with Xbal and Pstl.

Identify them using agarose gel electrophoresis.

Do the ligation and transformation.

8.13

Identify rbs+agn using electrophoresis.

Digest 1-23L with EcoRl and Xbal. Digest T7+merT+merP+merC with EcoRl and Spel.

Do the ligation and transformation.

8.14

Prepare the plasmid DNA.

Send the correct ones for sequencing.

8.15

See the sequencing result.

8.16

Digest PhiR73+Po promoter with EcoRl and Spel. Digest RBS with EcoRl and Xbal.

Retract the whole genome of K12 strain.

PCR antigen 43 using new template.

Pick single clones of antigen 43.

8.17

T7+TCP+Terminator done.

Transform it to BL21 strain.

Send antigen 43 for sequencing.

PCR antigen 43 using new template and better protocol.

Do the colony PCR of PhiR73+Po promoter+rbs.

Prepare the plasmid DNA and digest it for identification.

Do the ligation and transformation.

Digest pmerT+GFP with Spel and Pstl, digest TPC with Xbal and Pstl.

Digest pPbrA with Spel and Pstl. Digest rbs+T3 pol with Xbal and Pstl.

8.18

Retrieve the digested product .

Identify them using electrophoresis.

Pick the single clone of PCR of PhiR73+Po promoter+rbs, do the colony PCR.

Prepare the plasmid DNA.

Send the correct ones for sequencing.

Connect pPbra with rbs+T3 pol. Connect PhiR73+Po promoter+rbs with antigen 43.

Connect merp+GFP with TCP.

Do the ligation and transformation.

8.19

Identify them using electrophoresis.

Retrieve the gel.

Do the ligation and transformation.

PCR antigen 43. Digest it using EcoRl and Spel.

8.20

Pick the colony of PhiR73+Po promoter+rbs+antigen 43.

Put rbs+antigen 43 into PSB1A2 plasmid. Do the ligation and transformation.

Digest merp+GFP and T3 pol.

8.21

Identify the colony PCR product using electrophoresis.

Do the transformation.

Digest rbs+agn43 with EcoRl and Xbal. Digest PhiR73+Po promoter using EcoRl and Spel.

8.22

Do the autoaggregation assay of antigen 43.

Induce its expression by adding IPTG.

8.23

Do the autoaggregation assay.

8.25

Prepare the plasmid DNA for TPC+Terminator.

Send the correct ones for sequencing.

Construct pPbra using primers annealing.

8.26

Transform antigen 43.

8.27

Pick single clone of antigen 43.

Do the transformation of TPC+terminator.

Do the transformation of pPbrA.

Connect pBAD with rbs. Do the ligation and transformation.

8.30

Do the functional test of antigen 43.

Pick the clone of antigen 43.

Pick the clone of merP+GFP+TCP.

Do the ligation of pPbra+T3 pol again.

Pick the single clone of Pbad+rbs.

Do the transformation.

8.31

Send the correct merp+GFP and Pbad+rbs for sequencing.

Do the transformation.

Induce the expression of antigen 43.

September

[TOP]

9.1

Connect the antigen 43 into plasmid.

Send merP+GFP+TCP for sequencing.

Connect pPbra+T3 pol using primers annealing.

Do the ligation and transformation.

9.2

Prepare the plasmid DNA for rbs+agn43.

See the sequencing result of merp+GFP+TCP.

Pick the clone of pPbra+T3 pol.

9.3

Send the rbs+agn43 for sequencing.

Digest rbs+agn43 with EcoRl and Xbal. Digest PhiR73+Po promoter with EcoRl and Spel.

Pick the clone of pPbra+T3 pol. Prepare the plasmid DNA.

9.6

Do the PCR of antigen 43 using Hifi Taq DNA polymerase.

Digest merP+GFP+TCP with EcoRl and Spel. Put it into PSB3K3 backbone.

Connect pPbra+T3 pol with 1-23L. pick the single clone. Prepare the plasmid DNA.

Do the ligation and transformation.

Pick the clone of Pbad+T3 pol.

Make competent cell containing pc+merR+merp+rbs+T3pol. Transform T3 promoter into it.

Induce the expression using different concentration of IPTG.

Re-suspend the cell. Measure the GFP intensity by a microplate reader.

9.7

Digest merP+GFP+TCP with EcoRl and Pstl to put it into PSB3K3.

Send pbra+T3 pol+terminator for sequencing.

Identify the pBAD+T3 pol using electrophoresis.

Make competent cells of pc+merR+merp+rbs+T3pol.

Transform T3 promoter into it.

9.8

Re-suspend the cell.

Measure the GFP intensity using microplate reader.

PCR antigen 43 using hifi Taq DNA polymerase.

9.9

PCR Rbs+agn 43 using agn for/rev primer to identify it.

Digest the correct ones using EcoRl and Spel.

Send the correct ones for sequencing.

Transform T3 promoter into cells containing pc+merR+merp+rbs+T3pol.

Send pBAD+T3 pol for sequencing.

pPbra+T3pol+terminator done.

Measure the GFP intensity using a microplate reader.

9.12

Digest rbs+agn43 with EcoRl and Xbal. Digest PhiR73+Po promoter with EcoRl and Spel.

Identify them using electrophoresis.

Retrieve the gel.

Do the ligation and transformation.

Pick the clone. ===9.13===. Digest Antigen 43 with EcoRl and Xbal. Digest PhiR73+Po promoter+rbs with EcoRl and Spel.

Identify them using electrophoresis.

9.14

PCR antigen 43.

Get the candidate of rbs+agn43.

Send the correct ones for sequencing.

9.15

Put antigen 43 into PSB1A2.

Do the ligation and transformation.

9.16

Digest PSB1A2 and PSB1A3.

9.17

Digest PSB1C3 with EcoRI and Spel.

Digest antigen 43 with EcoRl and Spel.

Do the ligation and transformation.

9.21

Retract the whole genome of K12 strain.

9.22

Nest PCR of antigen 43 using new template and new primers.

Put antigen 43 into PSB1C3.

Pick the single clone of antigen 43.

9.23

Prepare the plasmid DNA for antigen43.

Digest the plasmid DNA using EcoRl and Spel.

Identify them using electrophoresis.

Make the competent cell contains PBAD+ T3 pol. Transform T3 promoter+GFP into it.

Pick the clone of PMERT+T3 pol.

Digest PSB3C5 using EcoRl and Pstl.

9.24

PSB3K5: EcoRl and Pstl.

T7+TPC+Ter: Xbal and Pstl.

MerP+GFP:EcoRl and Spel.

Do the ligation and transformation.

9.25

Retrieve the digested merp+GFP.

Induce the expression of PBAD+T3 pol using 10^-5 M arabinose.

Do the antigen 43 PCR using touchdown PCR.

Do the ligation and transformation.

9.26

Make the competent cell contains T3 promoter+GFP. Transform pmert+T3pol and 1-18i+merR.

Do the colony PCR to identify it.

9.27

Attend the seminar.

9.28

Connect T7+PhiR73+Po promoter+rbs+antigen 43.

Do the ligation and transformation.

PCR the T3 promoter+PhiR73+Po promoter.

9.29

Retrieve the PCR product.

Digest the product using EcoRl and Spel.

Digest TCP with Xbal and Pstl. Identify it using electrophoresis.

Digest merp+GFP using Spel and Pstl.

Do the transformation.

9.30

Do the ligation and transformation.

Prepare the plasmid DNA and identify it using PCR.

October

[TOP]

10.1

Digest pTET+T7 pol using EcoRl and Spel.

Retrieve the gel.

Connect T3 promoter+PhiR73+Po promoter+ antigen 43.

Do the ligation and transformation.

10.3

Connect pTET+T7 pol and T7 promoter+PhiR73+Po promoter+ antigen 43.

Do the ligation and transformation.

10.4

Do the auto-aggregation assay of antigen 43.

10.5

Do the auto-aggregation assay.

10.7

Digest merp+GFP using Spel and Pstl.

Digest TCP using Xbal and Pstl.

Do the ligation and transformation.

10.8

Identify the digested product using electrophoresis.

Do the ligation and transformation.

10.9

Prepare the plasmid DNA.

Identify them using PCR.

Send the correct ones for sequencing.

10.10

Antigen 43 clone step done.

Connect ptet+T7 pol with T7 promoter+PhiR73+Po promoter+ antigen 43.

Do the ligation and transformation.

10.11

Do the auto-aggregation assay.

10.12

Do the auto-aggregation assay.

10.13

Measure the result.

10.15

Attend group seminar.

Do the auto-aggregation assay.

10.16-10.21

Connect merp+GFP with TCP.

Connect pc+merR with terminator.

Transform these two plasmid into one single strain.

Antigen 43 auto-aggregation assay. Analyse the result.

10.21-10.25

Upload and edit parts of our group.

[TOP]

==go to his page==

@@ Line 25: / Line 25: @@
 <html>
 <img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>
-<a href="https://static.igem.org/mediawiki/2010/5/5e/Note-mjing.pdf"><font color=#FFFFFF>download her notes</font></a>
+<a href="https://static.igem.org/mediawiki/2010/5/5e/Note-mjing.pdf"><font color=#FFFFFF>download his notes</font></a>
 </html>
 =='''Contents'''==
-* <span style="font-size:4mm;">[[Team:Peking/Notebook/YHu#July| July, 2010]]</span>
+* <span style="font-size:4mm;">[[Team:Peking/Notebook/MJing#July| July, 2010]]</span>
-* <span style="font-size:4mm;">[[Team:Peking/Notebook/YHu#August| August, 2010]]</span>
+* <span style="font-size:4mm;">[[Team:Peking/Notebook/MJing#August| August, 2010]]</span>
-* <span style="font-size:4mm;">[[Team:Peking/Notebook/YHu#September| September, 2010]]</span>
+* <span style="font-size:4mm;">[[Team:Peking/Notebook/MJing#September| September, 2010]]</span>
-* <span style="font-size:4mm;">[[Team:Peking/Notebook/YHu#October| October, 2010]]</span>
+* <span style="font-size:4mm;">[[Team:Peking/Notebook/MJing#October| October, 2010]]</span>
@@ Line 97: / Line 97: @@
 |style="text-align:center"| -
 |}
-[[https://2010.igem.org/Team:Peking/Notebook/MJing TOP]]
+[<html><a href="#top">TOP</a></html>]
-===7.1===
+===7.3===
+Antigen 43 PCR, 20ul system. T3 polymerase PCR.
-. DNA double digestion of mbp fragments for 3 hours: NdeI/XhoI for commercialization and XbaI/PstI for standardization.
+Identify them by 1% agarose gel electrophoresis.
+===7.4===
+Antigen 43 PCR using different annealing temperature, with gradient 1 ℃.
-uL reaction system:
+Attend the group seminar.
-Buffer4    2uL
+Retrieve the PCR product of T3 polymerase and digest it with EcoRI and PstI. Digest for the whole night.
+===7.5===
+Identify the product by agarose gel electrophoresis. Retrieve the PCR product of Antigen 43.
-NdeI      1.5uL
+Retrieve the digested T3 polymerase and ligated it to the plasmid PSB1A2.
-XhoI      1.5uL
+Transform the plasmid to Trans 5α strain.
-mbp(com)   15uL
+PCR the antigen 43 with much larger annealing temperature gradient. Identify it with electrophoresis.
+===7.6===
+Design the primer of antigen 43 again by Primer Premier 5.0.
+===7.8===
+PCR antigen 43 using nest-PCR procedure. Using Taq DNA polymerase to do the first step nest PCR.
+Identify it by electrophoresis. Retrieve the 3k band and do the second step of nest PCR by using the product of the
+first step as template.
+===7.9===
+Identify the second PCR product by electrophoresis. Retrieve the 3k band and digest it with EcoRI and SpeI to put it
+into plasmid. Digest it with PstI to test whether this is antigen 43.( antigen 43 have 6 PstI digestion sites.)
-Buffer3    2uL
+Design the six point mutation primer.
+===7.10===
+Do the transformation and ligation.
+===7.12===
+Prepare plasmid DNA.
-XbaI      1.5uL
+Digest the plasmid DNA with PstI to identify it.
-PstI      1.5uL
+PCR the product using Easytaq DNA polymerase to identify the molecule weight of the product.
+===7.13===
+Learn to do the western blotting. Write the protocols.
-mbp(SD)   15uL
+Digest merT, merP and merC with Xbal and PstI. Meanwhile digest B0034(RBS) with SpeI and PstI.
-. DNA Purification.
+Connect the two digested product together.
-===7.17===
+Transform the ligation product into Trans5αstrain.
-. PCR reaction for mbp fragments using dissolved primers.
-Primers Reverse is the new ones with strepp tag.
+Pick the single clone from the plate.
-x easypfu buffer     2uL
+Send the PCR product of Antigen 43 for sequencing.
+===7.14===
+Prepare the plasmid DNA of rbs+merT, rbs+merP, rbs+merC.
-ddNTP Mixture        2uL
+Do the western blotting.
+===7.15===
+Digest the plasmid DNA by EcoRI and PstI to identify it.
-For                 1uL
+Digest rbs+merT with Spel and Pstl and digest rbs+merP with Xbal and Pstl.
-Rev                 1uL
+Identify them using agarose gel electrophoresis.
+===7.16===
+Connect rbs with merT, merP and merC again.
-Template plasmid      0.5uL
+Do the first point mutation. First PCR the antigen 43 gene with designed point mutation primers, then retrieve it by
+electrophoresis. Then do the blunting kination, finally do the ligation and put it into strains by transformation.
+===7.18===
+Prepare the plasmid DNA for rbs+merT, rbs+merP and rbs+merC, Antigen 43 mutant 1.
-phusionHF            0.2uL
+Identify them using electrophoresis.
-ddH2O               up to 20 uL
+Connect rbs+merT with rbs+merP.
-. Electrophoresis PCR reaction system in 1% agarose gel.
+Do the second step of point mutation for antigen 43. Do the PCR step. Identify it by electrophoresis.
+Blunting kination, ligation and transformation.
-. Excise the gel slice and extract the mbp fragments.
+Send the first point mutation product for sequencing.
-===7.18===
-. DNA double digestion of mbp fragments and merr plasmids.
-. ligation of insert DNA fragments into plasmid vector DNA for 1 hour
+The rbs+merT,rbs+merP and rbs+merC sequenced correct.
+===7.19===
+Retrieve the product of digested rbs+merT and rbs+merP by electrophoresis. Connect the rbs+merT with rbs+merP,. Do the transformation.
-mbp(NdeI/XhoI)     6uL
+Pick the single clone of antigen 43 second step point mutation strain.
+===7.20===
+Prepare the plasmid DNA of antigen 43 second point mutation strain. Send it for sequencing.
-pET-21a            2uL
+Do the third step point mutation.
-x ligation buffer    1uL
+Identify the plasmid DNA by electrophoresis. Retrieve the third point mutation PCR product by electrophoresis.
-T4 DNA Ligase       1uL
+Digest rbs+merT+rbs+merP with Spel and Pstl, digest rbs+merC with Xbal and Pstl.
+===7.21===
+Identify the product of the digestion using electrophoresis.
+Pick the single clone of the 3rd point mutation of antigen 43 strain on the plate.
+===7.22===
+Connect rbs+merT+rbs+merP with rbs+merC.
-mbp (Xbal/PstI)           6uL
+Using easyPFu to PCR antigen 43.The forward primer contains a rbs. Digest it with EcoRl and Spel to put it into PSB1A2 plasmid.
-B0034 (rbs)              2uL
+Prepare the plasmid DNA of the product of the third point mutation of antigen 43.digest it with EcoRl and SpeI to identify it.
-x ligation buffer         1uL
+Do the 4th point mutation PCR step.
+===7.23===
+Identify the plasmid using agarose gel electrophoresis.
-T4 DNA Ligase            1uL
+Send the plasmid DNA for sequencing.
+Put the rbs+agn43 into plasmid by ligation.
+===7.29===
+Attend the group seminar.
-merr (Xbal/PstI)          6uL
+Prepare the plasmid DNA for rbs+merT+rbs+merP+rbs+merC. Digest it with EcoRl and Pstl for identification. Digest it with Xbal and Pstl and digest the plasmid contains T7 promoter with Spel and Pstl.
-B0034 (rbs)              2uL
+Do the 5th point mutation of antigen 43. Do the PCR step.
-x ligation buffer         1uL
+Identify the product of the 4th point mutation and the rbs+merT+rbs+merP+rbs+merC by electrophoresis. Collect those correct ones and send them for sequencing.
-T4 DNA Ligase            1uL
+See the point mutation result in the sequence.
-. Transformation
+Identify the T7+rbs+merT+rbs+merP+rbs+merC by electrophoresis.
+===7.30===
+Digest rbs+agn43 with EcoRl and Xbal. Digest phiR73+Po promoter with EcoRl and Spel.
-===7.19===
+Retrieve the digested T7+rbs+merT+rbs+merP+rbs+merC gel.
-. Miniprep of rbs-merr
-. Digestion and identification by Electrophoresis
+Do the transformation.
+===7.31===
+Digest 2-2E constitutive promoter with EcoRl and Spel. Digest rbs+agn43 with EcoRl and Xbal.
-Buffer3    1uL
+Connect 2-2E promoter with rbs+agn43.
-XbaI      0.75uL
+==August==
-PstI       0.75uL
+{| class="calendar" border="0" rules="rows" width="650px" style="color:#ffffff"
+|-
+|style="text-align:center"| Mon
+|style="text-align:center"| Tue
+|style="text-align:center"| Wed
+|style="text-align:center"| Thu
+|style="text-align:center"| Fri
+|style="text-align:center"| Sat
+|style="text-align:center"| Sun
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.1|1]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.2|2]]
+|style="text-align:center"| 3
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.4|4]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.5|5]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.6|6]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.7|7]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.8|8]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#8.9|9]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.10|10]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.11|11]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.12|12]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.13|13]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.14|14]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.15|15]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.16|16]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.17|17]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.18|18]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.19|19]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.20|20]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.21|21]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.22|22]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.23|23]]
+|style="text-align:center"|24
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.25|25]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.26|26]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.27|27]]
+|style="text-align:center"| 28
+|-
+|style="text-align:center"| 29
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.30|30]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#8.31|31]]
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| -
+|}
+[<html><a href="#top">TOP</a></html>]
+===8.1===
+Prepare the plasmid DNA of T7+rbs+merT+rbs+merP+rbs+merC and PhiR73+Po promoter+rbs+antigen 43.
-rbs-merr   7.5uL
+Prepare the plasmid DNA of 2-2E promoter+rbs+antigen 43.
-===7.20===
+Identify PhiR73+Po promoter+rbs+antigen 43 and 2-2E promoter+rbs+antigen 43 using electrophoresis.
-Miniprep of 12 colonies of mbp-commercialization.
+===8.2===
+Send the correct ones for sequencing.
-No colonies formation of rbs-mbp.
+Digest rbs+antigen 43 again.
+===8.4===
+Pick the clone of PhiR73+Po promoter+rbs+antigen 43 on the plate for autoaggregation assay.
-===7.21===
+Plan the assay.
-. DNA double digestion of colonies of mbp-pET-21a and rbs-merr.
-uL reaction system:
+Design new primers for antigen 43 which contains different promoters in the forward primer.
+===8.5===
+Preliminary autoaggregation assay.
-Buffer4       1uL
+Send PhiR73+Po promoter+rbs+antigen 43 for sequencing.
-NdeI         0.75uL
+Transform PhiR73+Po promoter+rbs+antigen 43 into BL21 strains.
+===8.6===
+Pick the single clone.
-XhoI          0.75uL
+Induce the antigen 43 gene’s expression by adding 10^-5 M IPTG for 4 hours.
-mbp-pET-21a   7.5uL
+Do the auto-aggregation assay( for detail, see the inductive aggregation page or antigen 43 part.)
+PCR the rbs+agn43 using easyPFU.
-Buffer3    1uL
+Identify it using electrophoresis.
-XbaI      0.75uL
+Digest the PCR product using EcoRl and Spel to put it into PSB1A2.
-PstI       0.75uL
+Do the ligation and transformation.
-rbs-mbp   7.5uL
+Send some of the PCR product for sequencing.
+===8.7===
+Digest merT+merC with Spel and Pstl, digest merP with Xbal and Pstl.
-. Electrophoresis in 1% agarose gel.
+Retrieve the gel. Do the ligation.
-Sequence mbp_ commercialization
+Pick three clones of rbs+merP.
+===8.8===
+Prepare the plasmid DNA for rbs+merP and merT+merC.
-(The result is confirmed to be incorrect.)
+Pick single clones of merT+merP+merC. Do the colony PCR.
-. ligation of rbs-mbp-1 and 2 into plasmid vector T7 for 1 hour
+Retrieve the rbs+agn43.
-rbs-mbp(Xbal/PstI)     6uL
+Do the ligation and transformation.
+===8.9===
+PCR antigen 43.
-T7 vector(SpeI/PstI)     2uL
+Nest PCR using nest primers. Do the first step.identify it using electrophoresis.
+===8.10===
+PCR antigen 43 using nest primers. Using different template.
-x ligation buffer      1uL
+Using better template to run PCR.
-T4 DNA Ligase         1uL
+Do the transformation of antigen 43.
+===8.11===
+Retrieve the product of rbs+agn43. Digest it and do the ligation and transformation.
+===8.12===
+Pick the single clone of rbs+agn43.
-. Transformation
+Digest 1-23L with EcoRl and Xbal. Digest T7+merT+merP+merC with EcoRl and Spel.
-===7.22===
+Digest pmerT+GFP with Spel and Pstl, digest TPC with Xbal and Pstl.
-No colonies formation of T7-rbs-merr. Do ligation and transformation again.
-===7.23===
+Identify them using agarose gel electrophoresis.
-Picking colonies of T7-rbs-merr and shaking at 37℃ overnight.
-===7.24===
+Do the ligation and transformation.
-Problems existed in our experiment: The PCR reaction product cannot be verified. New primers forward (3C and 3Plus) for mbp fragments are designed.
+===8.13===
+Identify rbs+agn using electrophoresis.
-. PCR reaction for mbp fragments using dissolved primers.
+Digest 1-23L with EcoRl and Xbal. Digest T7+merT+merP+merC with EcoRl and Spel.
-For                    1uL
+Do the ligation and transformation.
+===8.14===
+Prepare the plasmid DNA.
-Rev                    1uL
+Send the correct ones for sequencing.
+===8.15===
+See the sequencing result.
+===8.16===
+Digest PhiR73+Po promoter with EcoRl and Spel. Digest RBS with EcoRl and Xbal.
-Easymix                 10uL
+Retract the whole genome of K12 strain.
-template                0.2uL
+PCR antigen 43 using new template.
-ddH2O                 up to 20 uL
+Pick single clones of antigen 43.
+===8.17===
+T7+TCP+Terminator done.
-. Miniprep of T7-rbs-merr
+Transform it to BL21 strain.
-. Digestion and identification by Electrophoresis
+Send antigen 43 for sequencing.
-EcoRI Buffer    1uL
+PCR antigen 43 using new template and better protocol.
-EcorRI        0.75uL
+Do the colony PCR of PhiR73+Po promoter+rbs.
-PstI          0.75uL
+Prepare the plasmid DNA and digest it for identification.
-T7-rbs-merr   7.5uL
+Do the ligation and transformation.
-The band was not correct.
+Digest pmerT+GFP with Spel and Pstl, digest TPC with Xbal and Pstl.
-===7.25===
+Digest pPbrA with Spel and Pstl. Digest rbs+T3 pol with Xbal and Pstl.
-. Electrophoresis PCR reaction product last day in 1% agarose gel.
+===8.18===
+Retrieve the digested product .
-. Excise the gel slice and extract the mbp fragments.
+Identify them using electrophoresis.
-. DNA double digestion of mbp fragments for 3 hours: Xbal/XhoI for commercialization and XbaI/PstI for standardization.
+Pick the single clone of PCR of PhiR73+Po promoter+rbs, do the colony PCR.
-uL reaction system:
+Prepare the plasmid DNA.
-Buffer4    2uL
+Send the correct ones for sequencing.
-Xbal      1.5uL
+Connect pPbra with rbs+T3 pol. Connect PhiR73+Po promoter+rbs with antigen 43.
-XhoI      1.5uL
+Connect merp+GFP with TCP.
-Product   15uL
+Do the ligation and transformation.
+===8.19===
+Identify them using electrophoresis.
+Retrieve the gel.
-Buffer3    2uL
+Do the ligation and transformation.
-XbaI      1.5uL
+PCR antigen 43. Digest it using EcoRl and Spel.
+===8.20===
+Pick the colony of PhiR73+Po promoter+rbs+antigen 43.
-PstI      1.5uL
+Put rbs+antigen 43 into PSB1A2 plasmid. Do the ligation and transformation.
-Product   15uL
+Digest merp+GFP and T3 pol.
+===8.21===
+Identify the colony PCR product using electrophoresis.
-. DNA Purification.
+Do the transformation.
-. ligation for 1 hour
+Digest rbs+agn43 with EcoRl and Xbal. Digest PhiR73+Po promoter using EcoRl and Spel.
+===8.22===
+Do the autoaggregation assay of antigen 43.
-mbp(XbaI/XhoI)     6uL
+Induce its expression by adding IPTG.
+===8.23===
+Do the autoaggregation assay.
+===8.25===
+Prepare the plasmid DNA for TPC+Terminator.
-pET-21a            2uL
+Send the correct ones for sequencing.
-x ligation buffer    1uL
+Construct pPbra using primers annealing.
+===8.26===
+Transform antigen 43.
+===8.27===
+Pick single clone of antigen 43.
-T4 DNA Ligase       1uL
+Do the transformation of TPC+terminator.
+Do the transformation of pPbrA.
-mbp (Xbal/PstI)           6uL
+Connect pBAD with rbs. Do the ligation and transformation.
+===8.30===
+Do the functional test of antigen 43.
-B0034 (rbs)              2uL
+Pick the clone of antigen 43.
-x ligation buffer         1uL
+Pick the clone of merP+GFP+TCP.
-T4 DNA Ligase            1uL
+Do the ligation of pPbra+T3 pol again.
-===7.26===
+Pick the single clone of Pbad+rbs.
-Transformation of ligation mixure.
-Name of plates were: 3C-com, 3Plus-com, 3C-SD, 3plus-SD
+Do the transformation.
+===8.31===
+Send the correct merp+GFP and Pbad+rbs for sequencing.
-*com means commercialization and SD means standardization
+Do the transformation.
-===7.27-7.28===
+Induce the expression of antigen 43.
-No colonies formation of 3C-com and 3plus-com
-. Picking 18 colonies from 3C-SD and 3plus-SD(mbp_SD) and shaking at 37℃ for 10 hours.
+==September==
-. Miniprep mbp_SD
+{| class="calendar" border="0" rules="rows" width="650px" style="color:#ffffff"
+|-
+|style="text-align:center"| Mon
+|style="text-align:center"| Tue
+|style="text-align:center"| Wed
+|style="text-align:center"| Thu
+|style="text-align:center"| Fri
+|style="text-align:center"| Sat
+|style="text-align:center"| Sun
+|-
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.1|1]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.2|2]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.3|3]]
+|style="text-align:center"| 4
+|style="text-align:center"|5
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.6|6]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.7|7]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.8|8]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.9|9]]
+|style="text-align:center"| 10
+|style="text-align:center"| 11
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.12|12]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.13|13]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.14|14]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.15|15]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.16|16]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.17|17]]
+|style="text-align:center"| 18
+|style="text-align:center"|  19
+|-
+|style="text-align:center"| 20
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.21|21]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.22|22]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.23|23]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.24|24]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.25|25]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.26|26]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.27|27]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#9.28|28]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.29|29]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#9.30|30]]
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| -
+|}
+[<html><a href="#top">TOP</a></html>]
+===9.1===
+Connect the antigen 43 into plasmid.
-. Digestion and identification by Electrophoresis
+Send merP+GFP+TCP for sequencing.
-EcoRI Buffer    1uL
+Connect pPbra+T3 pol using primers annealing.
-EcorRI        0.75uL
+Do the ligation and transformation.
+===9.2===
+Prepare the plasmid DNA for rbs+agn43.
-PstI          0.75uL
+See the sequencing result of merp+GFP+TCP.
-mbp_SD      7.5uL
+Pick the clone of pPbra+T3 pol.
+===9.3===
+Send the rbs+agn43 for sequencing.
-Sequence.
+Digest rbs+agn43 with EcoRl and Xbal. Digest PhiR73+Po promoter with EcoRl and Spel.
-(The result is confirmed to be incorrect.)
+Pick the clone of pPbra+T3 pol. Prepare the plasmid DNA.
+===9.6===
+Do the PCR of antigen 43 using Hifi Taq DNA polymerase.
-===7.30===
+Digest merP+GFP+TCP with EcoRl and Spel. Put it into PSB3K3 backbone.
-Template of pASK-mbp is verified to have mutagenesis; therefore we decide to construct mbp by linking 2 merr fragments together.
-. PCR reaction for six merr fragments: N_B and B_X; SD(Xbal)_B and B_SD(PstI); SD(EcoRI)_B and B_SD(PstI).
+Connect pPbra+T3 pol with 1-23L. pick the single clone. Prepare the plasmid DNA.
-x buffer              5uL
+Do the ligation and transformation.
-ddNTP Mixture           5uL
+Pick the clone of Pbad+T3 pol.
-For                    1uL
+Make competent cell containing pc+merR+merp+rbs+T3pol. Transform T3 promoter into it.
-Rev                    1uL
+Induce the expression using different concentration of IPTG.
-Template plasmid         0.5uL
+Re-suspend the cell. Measure the GFP intensity by a microplate reader.
+===9.7===
+Digest merP+GFP+TCP with EcoRl and Pstl to put it into PSB3K3.
-Polymerase              1uL
+Send pbra+T3 pol+terminator for sequencing.
-ddH2O                 up to 50 uL
+Identify the pBAD+T3 pol using electrophoresis.
-. Electrophoresis PCR reaction system in 1% agarose gel to identification.
+Make competent cells of pc+merR+merp+rbs+T3pol.
-. DNA purification from reaction mixture.
+Transform T3 promoter into it.
+===9.8===
+Re-suspend the cell.
-. DNA double digestion for 3 hours.
+Measure the GFP intensity using microplate reader.
-uL reaction system:
+PCR antigen 43 using hifi Taq DNA polymerase.
+===9.9===
+PCR Rbs+agn 43 using agn for/rev primer to identify it.
-N_B:
+Digest the correct ones using EcoRl and Spel.
-Buffer3    2uL
+Send the correct ones for sequencing.
-NdeI      1.5uL
+Transform T3 promoter into cells containing pc+merR+merp+rbs+T3pol.
-BamHI    1.5uL
+Send pBAD+T3 pol for sequencing.
-Product   15uL
+pPbra+T3pol+terminator done.
-B_X:
+Measure the GFP intensity using a microplate reader.
+===9.12===
+Digest rbs+agn43 with EcoRl and Xbal. Digest PhiR73+Po promoter with EcoRl and Spel.
-Buffer3    2uL
+Identify them using electrophoresis.
-BamHI    1.5uL
+Retrieve the gel.
-XhoI      1.5uL
+Do the ligation and transformation.
-Product   15uL
+Pick the clone.
+===9.13===.
+Digest Antigen 43 with EcoRl and Xbal. Digest PhiR73+Po promoter+rbs with EcoRl and Spel.
-SD(Xbal)_B:
+Identify them using electrophoresis.
+===9.14===
+PCR antigen 43.
-Buffer3    2uL
+Get the candidate of rbs+agn43.
-XbaI      1.5uL
+Send the correct ones for sequencing.
+===9.15===
+Put antigen 43 into PSB1A2.
-BamHI    1.5uL
+Do the ligation and transformation.
+===9.16===
+Digest PSB1A2 and PSB1A3.
+===9.17===
+Digest PSB1C3 with EcoRI and Spel.
-Product   15uL
+Digest antigen 43 with EcoRl and Spel.
-B_SD(PstI):
+Do the ligation and transformation.
+===9.21===
+Retract the whole genome of K12 strain.
+===9.22===
+Nest PCR of antigen 43 using new template and new primers.
-Buffer3    2uL
+Put antigen 43 into PSB1C3.
-BamHI     1.5uL
+Pick the single clone of antigen 43.
+===9.23===
+Prepare the plasmid DNA for antigen43.
-PstI      1.5uL
+Digest the plasmid DNA using EcoRl and Spel.
-Product   15uL
+Identify them using electrophoresis.
-SD(EcoRI)_B:
+Make the competent cell contains PBAD+ T3 pol. Transform T3 promoter+GFP into it.
-EcoRI Buffer    2uL
+Pick the clone of PMERT+T3 pol.
-EcorRI       1.5uL
+Digest PSB3C5 using EcoRl and Pstl.
+===9.24===
+PSB3K5: EcoRl and Pstl.
-BamHI       1.5uL
+T7+TPC+Ter: Xbal and Pstl.
-Product      15uL
+MerP+GFP:EcoRl and Spel.
-. DNA purification after the double digestion.
+Do the ligation and transformation.
+===9.25===
+Retrieve the digested merp+GFP.
-. ligation of 2 merr fragments into the vector for 6 hours.
+Induce the expression of PBAD+T3 pol using 10^-5 M arabinose.
-Insert1              3uL
+Do the antigen 43 PCR using touchdown PCR.
-Insert2              3uL
+Do the ligation and transformation.
+===9.26===
+Make the competent cell contains T3 promoter+GFP. Transform pmert+T3pol and 1-18i+merR.
-Vector               2uL
+Do the colony PCR to identify it.
+===9.27===
+Attend the seminar.
+===9.28===
+Connect T7+PhiR73+Po promoter+rbs+antigen 43.
-x ligation buffer      1uL
+Do the ligation and transformation.
-T4 DNA Ligase         1uL
+PCR the T3 promoter+PhiR73+Po promoter.
+===9.29===
+Retrieve the PCR product.
-mbp-Com: Inserts: N_B and B_X; vector: pET-21a(NdeI/Xhol)
+Digest the product using EcoRl and Spel.
-mbp-SD: Inserts: SD(Xbal)_B and B_SD(PstI), vector:B0034(SpeI/PstI)
+Digest TCP with Xbal and Pstl. Identify it using electrophoresis.
-mbp: SD(EcoRI)_B and B_SD(PstI), vector: pSB1K3 (EcoRI/PstI)
+Digest merp+GFP using Spel and Pstl.
-. Transformation
+Do the transformation.
+===9.30===
+Do the ligation and transformation.
-===7.31===
+Prepare the plasmid DNA and identify it using PCR.
-No colonies formation of mbp-Com.
-. Picking colonies from mbp-SD and mbp, shaking at 37℃ for 10 hours.
+==October==
-. Miniprep of mbp-SD and mbp
+{| class="calendar" border="0" rules="rows" width="650px" style="color:#ffffff"
+|-
+|style="text-align:center"| Mon
+|style="text-align:center"| Tue
+|style="text-align:center"| Wed
+|style="text-align:center"| Thu
+|style="text-align:center"| Fri
+|style="text-align:center"| Sat
+|style="text-align:center"| Sun
+|-
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"|-
+|style="text-align:center"|-
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.1|1]]
+|style="text-align:center"|2
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.3|3]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.4|4]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.5|5]]
+|style="text-align:center"|6
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.7|7]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.8|8]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.9|9]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.10|10]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.11|11]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.12|12]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.13|13]]
+|style="text-align:center"|14
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.15|15]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.16-10.21|16]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.16-10.21|17]]
+|-
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.16-10.21|18]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.16-10.21|19]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.16-10.20|20]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.21-10.25|21]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.21-10.25|22]]
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.21-10.25|23]]
+|style="text-align:center"| [[Team:Peking/Notebook/MJing#10.21-10.25|24]]
+|-
+|style="text-align:center"|[[Team:Peking/Notebook/MJing#10.21-10.25|25]]
+|style="text-align:center"|-
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| -
+|style="text-align:center"| -
+|}
+[<html><a href="#top">TOP</a></html>]
+===10.1===
+Digest pTET+T7 pol using EcoRl and Spel.
-. Miniprep of B0034
+Retrieve the gel.
-. Double digestion for 3 hours.
+Connect T3 promoter+PhiR73+Po promoter+ antigen 43.
-Buffer2    2uL
+Do the ligation and transformation.
+===10.3===
+Connect pTET+T7 pol and T7 promoter+PhiR73+Po promoter+ antigen 43.
-SpeI     1.5uL
+Do the ligation and transformation.
+===10.4===
+Do the auto-aggregation assay of antigen 43.
+===10.5===
+Do the auto-aggregation assay.
+===10.7===
+Digest merp+GFP using Spel and Pstl.
-PstI      1.5uL
+Digest TCP using Xbal and Pstl.
-B0034(rbs)    5uL
+Do the ligation and transformation.
+===10.8===
+Identify the digested product using electrophoresis.
-ddH2O   up to 20 uL
+Do the ligation and transformation.
+===10.9===
+Prepare the plasmid DNA.
+Identify them using PCR.
+Send the correct ones for sequencing.
+===10.10===
+Antigen 43 clone step done.
+Connect ptet+T7 pol with T7 promoter+PhiR73+Po promoter+ antigen 43.
+Do the ligation and transformation.
+===10.11===
+Do the auto-aggregation assay.
+===10.12===
+Do the auto-aggregation assay.
+===10.13===
+Measure the result.
+===10.15===
+Attend group seminar.
+Do the auto-aggregation assay.
+===10.16-10.21===
+Connect merp+GFP with TCP.
+Connect pc+merR with terminator.
+Transform these two plasmid into one single strain.
+Antigen 43 auto-aggregation assay.  Analyse the result.
+===10.21-10.25===
+Upload and edit parts of our group.
+[<html><a href="#top">TOP</a></html>]
+<html>
+</div>
+<div id="project description bottom">
+<div id="bottomgreen">
+<br>
+<a href="https://2010.igem.org/Team:Peking/Team/MJing"><font color=#FFFFFF>==go to his page==</font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
+</div>
+</html>

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	-	-	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	26	27	28	29	30	31
-	-	-	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
1	2	3	4	5	6	7
8	9	10	11	12	13	14
15	16	17	18	19	20	21
22	23	24	25	26	27	28
29	30	31	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	1	2	3	4	5
6	7	8	9	10	11	12
13	14	15	16	17	18	19
20	21	22	23	24	25	26
27	28	29	30	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	-	-	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	-	-	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	-	-	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	26	27	28	29	30	31
-	-	-	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
1	2	3	4	5	6	7
8	9	10	11	12	13	14
15	16	17	18	19	20	21
22	23	24	25	26	27	28
29	30	31	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	1	2	3	4	5
6	7	8	9	10	11	12
13	14	15	16	17	18	19
20	21	22	23	24	25	26
27	28	29	30	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	-	-	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	-	-	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	-	-	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	26	27	28	29	30	31
-	-	-	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
1	2	3	4	5	6	7
8	9	10	11	12	13	14
15	16	17	18	19	20	21
22	23	24	25	26	27	28
29	30	31	-	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	1	2	3	4	5
6	7	8	9	10	11	12
13	14	15	16	17	18	19
20	21	22	23	24	25	26
27	28	29	30	-	-	-

Mon	Tue	Wed	Thu	Fri	Sat	Sun
-	-	-	-	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	-	-	-	-	-	-