Difference between revisions of "Team:UBonn HBRS/Description/Notebook/2016"
| Line 17: | Line 17: | ||
Repetion of restriction analysis from the genes KW10 and gel clean ups of the linkers. | Repetion of restriction analysis from the genes KW10 and gel clean ups of the linkers. | ||
| − | Deinking: | + | Deinking: <br /> |
| − | *Measurement of inkjet absorbance spectrum | + | * Measurement of inkjet absorbance spectrum |
| − | *filtration-based deinking setup | + | * filtration-based deinking setup |
<html></div></html> | <html></div></html> | ||
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<html><div class="panel notebook-entry"></html> | <html><div class="panel notebook-entry"></html> | ||
==12KW (21.3-27.3)== | ==12KW (21.3-27.3)== | ||
| − | |||
repetition of restriction analysis of all genes and gel clean ups of the genes. | repetition of restriction analysis of all genes and gel clean ups of the genes. | ||
| − | Deinking: | + | Deinking: <br /> |
inkjet ink absorbance spectrum and pulp preparation | inkjet ink absorbance spectrum and pulp preparation | ||
<html></div></html> | <html></div></html> | ||
| Line 176: | Line 175: | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==29KW (18.7-24.7)== | ==29KW (18.7-24.7)== | ||
| − | Deinking: | + | Deinking: <br /> |
separation of ink from fibers in organic phase of big scale deinking, flotation-based deinking, foam collection, defoaming | separation of ink from fibers in organic phase of big scale deinking, flotation-based deinking, foam collection, defoaming | ||
| + | <html></div></html> | ||
| − | + | <html><div class="panel notebook-entry"></html> | |
==30KW (25.7-31.7)== | ==30KW (25.7-31.7)== | ||
| − | Deinking: | + | Deinking: <br /> |
tests with toluene flotation-based deinking | tests with toluene flotation-based deinking | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==31KW (1.8-7.8)== | ==31KW (1.8-7.8)== | ||
| − | + | Ligation of Fragment synthesized at IDT and C3. <br /> | |
| − | Ligation of Fragment synthesized at IDT and C3 | + | Ligation of genes in C3 and genes + tags + C5. <br /> |
| − | Ligation of genes in C3 and genes + tags + C5 | + | |
transformation, and inoculation of liquid cultures of the above. | transformation, and inoculation of liquid cultures of the above. | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==32KW (8.8 - 14.8)== | ==32KW (8.8 - 14.8)== | ||
| + | Ligation of IDT and C3. <br /> | ||
| + | Transformation and inoculation. <br /> | ||
| + | Minipreps of samples and restriction analysis. | ||
| − | + | Ligations of genes plus tags in bb_MCS. <br /> | |
| − | + | Transformation of these samples. | |
| − | + | <html></div></html> | |
| − | + | ||
| − | Ligations of genes plus tags in bb_MCS | + | |
| − | Transformation of these samples | + | |
| + | <html><div class="panel notebook-entry"></html> | ||
==33KW (15.8 - 21.8)== | ==33KW (15.8 - 21.8)== | ||
| − | + | Inoculation and miniprep. <br /> | |
| − | Inoculation and miniprep | + | Repetion of ligation of IDT and C3. <br /> |
| − | Repetion of ligation of IDT and C3 | + | Repetion of ligation of bb + nprb + genes. <br /> |
| − | Repetion of ligation of bb + nprb + genes | + | Midi prep of SacB, bb and nprb. <br /> |
| − | Midi prep of SacB, bb and nprb | + | Ligation of Genes + C5 and genes plus tags in C5. <br /> |
| − | Ligation of Genes + C5 and genes plus tags in C5. | + | Transformation and inoculation of the samples. <br /> |
| − | Transformation and inoculation of the samples. | + | |
mini preps | mini preps | ||
| − | Deinking: | + | |
| + | Deinking: <br /> | ||
creation of flat paper-like discs | creation of flat paper-like discs | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==34KW (22.8 - 28.8)== | ==34KW (22.8 - 28.8)== | ||
| − | |||
Restrictions of mini prep and repetition of mini prep | Restrictions of mini prep and repetition of mini prep | ||
| − | Deinking: | + | Deinking: <br /> |
grayscale tests with officer scanner and odisey scanner | grayscale tests with officer scanner and odisey scanner | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==35KW (29.8 - 4.9)== | ==35KW (29.8 - 4.9)== | ||
| + | <html></div></html> | ||
| + | |||
| + | |||
| + | <html><div class="panel notebook-entry"></html> | ||
==36KW (5.8 - 11.8)== | ==36KW (5.8 - 11.8)== | ||
| − | Deinking: | + | Deinking: <br /> |
tests of water controls | tests of water controls | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==37KW (12.9 - 18.9)== | ==37KW (12.9 - 18.9)== | ||
| − | Deinking: | + | Deinking: <br /> |
scanning tests, different conditions tests | scanning tests, different conditions tests | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==38KW (19.9 - 25.9)== | ==38KW (19.9 - 25.9)== | ||
| + | |||
| + | <html></div></html> | ||
| + | |||
| + | |||
| + | <html><div class="panel notebook-entry"></html> | ||
==39KW (26.8 - 2.10)== | ==39KW (26.8 - 2.10)== | ||
| − | Deinking: | + | Deinking: <br /> |
establishing water and standard controls into setup with kitchen mixer | establishing water and standard controls into setup with kitchen mixer | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==40KW (3.10 - 9.10)== | ==40KW (3.10 - 9.10)== | ||
| − | Deinking: | + | Deinking: <br /> |
xylanase started to test + cb | xylanase started to test + cb | ||
| + | <html></div></html> | ||
| + | <html><div class="panel notebook-entry"></html> | ||
==41KW (10.10 - 16.10)== | ==41KW (10.10 - 16.10)== | ||
| − | Deinking: | + | Deinking: <br /> |
xyl tests + cb | xyl tests + cb | ||
| − | + | <html></div></html> | |
| − | + | ||
{{UBonn_HBRS/footer|class-sideNav=hidden}} | {{UBonn_HBRS/footer|class-sideNav=hidden}} | ||
Revision as of 01:04, 19 October 2016
Lab Notebook 2016
Contents
- 1 10KW (7.3-13.3)
- 2 11KW (14.3-20.3)
- 3 12KW (21.3-27.3)
- 4 13KW (28.3-3.4)
- 5 14KW (4.4-10.4)
- 6 15KW (11.4-17.4)
- 7 16KW (18.4-24.4)
- 8 17KW (25.4-1.5)
- 9 18KW (2.5-8.5)
- 10 19KW (9.5-15.5)
- 11 20KW (16.5-22.5)
- 12 21KW (23.5-29.5)
- 13 22KW (30.5-5.6)
- 14 23KW (6.6-12.6)
- 15 24KW (13.6-19.6)
- 16 25KW (20.6-26.6)
- 17 26KW (27.6 - 3.7)
- 18 28KW (11.7-17.7)
- 19 29KW (18.7-24.7)
- 20 30KW (25.7-31.7)
- 21 31KW (1.8-7.8)
- 22 32KW (8.8 - 14.8)
- 23 33KW (15.8 - 21.8)
- 24 34KW (22.8 - 28.8)
- 25 35KW (29.8 - 4.9)
- 26 36KW (5.8 - 11.8)
- 27 37KW (12.9 - 18.9)
- 28 38KW (19.9 - 25.9)
- 29 39KW (26.8 - 2.10)
- 30 40KW (3.10 - 9.10)
- 31 41KW (10.10 - 16.10)
10KW (7.3-13.3)
transformation of genes bought at genescript: XynA, XynB, LipA, EstC2, CpCel9, CpCel5c, EngB, CelA, BsCel5, Bpul and Linkers: nprb, SacB inoculation of liquid cultures and restriction Analysi of linkers (SacB and nprb).
repetition of the transformation for XynB, EngB and linkers. Subsequently inoculation and miniprep of the samples. Preparation of glycerol stock.
restriction analysis of the genes.
11KW (14.3-20.3)
Repetion of restriction analysis from the genes KW10 and gel clean ups of the linkers.
Deinking:
- Measurement of inkjet absorbance spectrum
- filtration-based deinking setup
12KW (21.3-27.3)
repetition of restriction analysis of all genes and gel clean ups of the genes.
Deinking:
inkjet ink absorbance spectrum and pulp preparation
13KW (28.3-3.4)
Restrictions and gel clean ups of all genes genes for a new gel clean up, because the ones of KW13 did not works. Ligation of genes from the gel clean ups into C3 and inoculation of cultures and minipreps. (1.04.16 :) → successful ligation of
- XynA
- CelA
- LipA
- Bpul
- CpCel5c
- BsCel5
- EstC2
- EngB in C3
- nprb + CpCel9
- nprb + BsCel5 in C3
Deinking:
establishing the set up and starting experiments with different conc of NaOH and Na2SiO3
14KW (4.4-10.4)
Deinking:
Experiments with different concentrations of surfactant oleic acid
15KW (11.4-17.4)
Deinking:
experiments with different incubation time, vortexing time, temperature
16KW (18.4-24.4)
Deinking:
tests with solvents to dissolve ink and fibers
17KW (25.4-1.5)
Deinking:
grayscale tests, solvent tests
18KW (2.5-8.5)
Deinking:
pulp preparation
19KW (9.5-15.5)
Deinking:
establishing water and standard chemical controls
20KW (16.5-22.5)
Deinking:
establishing water and standard chemical controls
21KW (23.5-29.5)
Restriction analysis of genes from the 13KW and mini prep from samples of the 13KW. (28.05.16) successful ligation of:
- nprb and sacB in C3
- nprb + EstC2 in C3
Deinking:
establishing oleic acid and oleic acid + citrate buffer controls
22KW (30.5-5.6)
Restriction analysis of samples of the 21KW
Deinking:
discovery: paper discs with CB turn red, tests to find the reason
23KW (6.6-12.6)
Inoculation of all genes from glycerol stocks and miniprep. Restriction analysis and gel clean up of the genes, ligation of the missing genes with C3.
Deinking:
tests with oleic acid and oleic acid + cb controls
24KW (13.6-19.6)
Restriction of bbMCS and gel clean ups.
Ligations of genes in C5 and C3.
Ligation of genes and tags in C5.
Minipreps of all of the samples.
Deinking:
tests with shaking during incubation and different incubation time
25KW (20.6-26.6)
Restriction analysis of the constructs
Repetition of ligation of genes in C5 and transformation and preps.
Deinking:
rotation evaporator concentrating ink
26KW (27.6 - 3.7)
Restriction analysis of the mini preps.
28KW (11.7-17.7)
Repetion of Ligations of genes and C5
Deinking:
flotation-based deinking, pulp preparation
29KW (18.7-24.7)
Deinking:
separation of ink from fibers in organic phase of big scale deinking, flotation-based deinking, foam collection, defoaming
30KW (25.7-31.7)
Deinking:
tests with toluene flotation-based deinking
31KW (1.8-7.8)
Ligation of Fragment synthesized at IDT and C3.
Ligation of genes in C3 and genes + tags + C5.
transformation, and inoculation of liquid cultures of the above.
32KW (8.8 - 14.8)
Ligation of IDT and C3.
Transformation and inoculation.
Minipreps of samples and restriction analysis.
Ligations of genes plus tags in bb_MCS.
Transformation of these samples.
33KW (15.8 - 21.8)
Inoculation and miniprep.
Repetion of ligation of IDT and C3.
Repetion of ligation of bb + nprb + genes.
Midi prep of SacB, bb and nprb.
Ligation of Genes + C5 and genes plus tags in C5.
Transformation and inoculation of the samples.
mini preps
Deinking:
creation of flat paper-like discs
34KW (22.8 - 28.8)
Restrictions of mini prep and repetition of mini prep
Deinking:
grayscale tests with officer scanner and odisey scanner
35KW (29.8 - 4.9)
36KW (5.8 - 11.8)
Deinking:
tests of water controls
37KW (12.9 - 18.9)
Deinking:
scanning tests, different conditions tests
38KW (19.9 - 25.9)
39KW (26.8 - 2.10)
Deinking:
establishing water and standard controls into setup with kitchen mixer
40KW (3.10 - 9.10)
Deinking:
xylanase started to test + cb
41KW (10.10 - 16.10)
Deinking:
xyl tests + cb
