Team:Peking S/lab/notebook/xjy

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Jingyi Xi's Notebook

summary

Mainly in charge of microfluidic device, I create a two-layered high-throughput microfluidic system for our project, which provides a suitable space for different cells to be separated apart and population controlled, as well as allowing chemical wires to transfer freely from each side to the other. What’s more, I also take part in molecular cloning of TPP regulator, characterization of chemical wire toolbox, and modeling work of XOR gate.

Contents

June, 2011

July, 2011

August, 2011

September, 2011

October, 2011

June

6.25

Design and draw blueprint of the first chip.

6.26

Do the photoetching of the first chip and mould the PDMS.

6.27

Make chips and test under microscope. Pick the relatively suitable size of chamber.

6.28

Design and draw blueprint of the second chip.

6.29

Do the photoetching of the second chip and mould the PDMS.

6.30

Make chips and test under microscope.

July

7.1

Change the flow velocity and test the chip under microscope, mould new chips.

7.2

Make chips and test under microscope with slowed flow velocity, mould new chips.

7.3

Test under microscope with slowed flow velocity and add a heater (37℃) to the system, the chip works well. Mould new chips.

7.4

Make chips and shoot a film of the growing cells in the chamber.

7.5

Design and draw blueprint of the third chip,which has wider channels and two kinds of chamber sizes.

7.6

Do the photoetching of the third chip and mould the PDMS.

7.7

Try the two-layered chips with a membrane beside each side of chips.

7.8

Try to use photoetching machine to align the markers on the chips.

7.9

Try to use common microscope to align the markers on the chips, by hands, successfully. Take photos of both sides (RFP and GFP) under fluorescence microscope.

7.10

Design and draw blueprint of the fourth chip,with longer channels.

7.11

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.12

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.13

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.14

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.15

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.16

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.17

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.18

Do the ligation of TPP_gfp, as well as the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.19

Do the extraction of whole genome of Streptomyces and extract AfsA and ArpA from it, keep on doing ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.20

Do the ligation of PBAD_TPP_gfp, as well as the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp.

7.21

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.22

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.23

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.24

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.25

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.26

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.27

Do the ligation of PBAD_AfsA, Pc_ArpA, Pqrr_gfp, and send plasmid of PBAD_TPP_gfp for sequencing.

7.28

The sequencing of PBAD_TPP_gfp is right, do the transformation of this part to DH5α, as well as cultivating the old E.coli containing this part in Lysogeny broth (containing ampicillin).

7.29

Cultivate the newly transformational E.coli in Lysogeny broth (containing ampicillin) and induce it with different density of TPP and under different conditions.

7.30

Cultivate the newly transformational E.coli in Lysogeny broth (containing ampicillin) and induce it with different density of TPP and under different conditions.

7.31

Cultivate the newly transformational E.coli in Lysogeny broth (containing ampicillin) and induce it with different density of TPP and under different conditions.

August

8.1

8.2

8.3

8.4

8.5

8.6

8.7

8.8

8.9

8.10

8.11

8.12

8.15

8.16

8.17

8.18

8.19

8.20

8.21

8.22

8.23

8.24

8.25

8.26

8.27

8.28

8.29

8.30

8.31

September

9.1

9.2

9.3

9.4

9.5

9.6

9.7

9.8

9.9

9.10

9.11

9.12

9.13

9.14

9.15

9.16

9.17

9.18

9.19

9.20

9.21

9.22

9.23

9.24

9.25

9.26

9.27

9.28

9.29

9.30

October

10.1

10.3

10.4

10.5

10.7

10.8

10.9

10.10

10.11

10.12

10.13

10.15

10.16-10.21

10.21-10.25

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