Team:Heidelberg/Templates/Del week13 G
From 2013.igem.org
(Difference between revisions)
(→Re-PCR from FS_10 to FS_23; 3.3 kb; 13-07-2013) |
(→Restriction digest of Fragment FS_08 to FS_23; 6.5 kb; 23-07-2013 with BglII) |
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==26-07-2013== | ==26-07-2013== | ||
- | ===Restriction digest of Fragment FS_08 to FS_23; 6.5 kb; | + | ===Restriction digest of Fragment FS_08 to FS_23; 6.5 kb; 23-07-2013 with BglII=== |
[[File:Heidelberg_20130726 2,5µllog2 AEEcoRIHF AFEcoRIHF GBGlII OPEcoRIHFbesch.png|150px|thumb|Restriction digest of DelAE (FS_02 to FS_03 ;08.07), DelAF (FS_02 to FS_05; 04.07) and DelOP (FS_22 to FS_13short ;21.07) with EcoRI-HF and digest of DelG (FS_08 to FS_23 cut1 ;23.07) with BglII; run at 100 V, 0.8 % gel (TAE)]] | [[File:Heidelberg_20130726 2,5µllog2 AEEcoRIHF AFEcoRIHF GBGlII OPEcoRIHFbesch.png|150px|thumb|Restriction digest of DelAE (FS_02 to FS_03 ;08.07), DelAF (FS_02 to FS_05; 04.07) and DelOP (FS_22 to FS_13short ;21.07) with EcoRI-HF and digest of DelG (FS_08 to FS_23 cut1 ;23.07) with BglII; run at 100 V, 0.8 % gel (TAE)]] | ||
Line 224: | Line 224: | ||
! what !! µl | ! what !! µl | ||
|- | |- | ||
- | | FS_08 to FS_23 cut1 ( | + | | FS_08 to FS_23 cut1 (23-07-2013) || 15 |
|- | |- | ||
| BglII || 0.5 | | BglII || 0.5 |
Latest revision as of 18:29, 3 October 2013
Contents |
22-07-2013
Re-PCR from FS_10 to FS_23; 3.3 kb; 13-07-2013
- Reaction
what | µl |
---|---|
Fragment FS_10 to FS_11_short (13-07-2013) | 1 |
FS_10: (1/10) | 2 |
FS_23: (1/10) | 2 |
Phusion flash Master Mix | 10 |
DMSO | 1 |
dd H2O | 4 |
- Conditions
--> First cycles with wrong program
Biorad C1000 Touch Block A | ||
---|---|---|
Cycles | temperature [°C] | Time [s] |
1 | 98 | 10 |
12 | 98 | 1 |
68 ↓ 0.5 | 5 | |
72 | 1:10 min | |
18 | 98 | 1 |
66 | 5 | |
72 | 1:10 min | |
1 | 72 | 5 min |
1 | 12 | inf |
Results:
- Re-Amplification of DelG lead to the expected fragment but also to a smear, therefore fragment will not be used for Gibson Assembly but restriction digests to validate the product.
Amplification from FS_08 to FS_23; 6.5 kb
- Reaction
what | µl |
---|---|
D. acidovorans DSM-39 | 1 |
FS_08: (1/10) | 2 |
FS_23: (1/10) | 2 |
Phusion flash Master Mix | 10 |
DMSO | 1/- |
dd H2O | 4/- |
- Conditions
Biorad MyCycler* | ||
---|---|---|
Cycles | temperature [°C] | Time [s] |
1 | 98 | 10 |
12 | 98 | 1 |
66 ↓ 0.5 | 5 | |
72 | 3:20 | |
18 | 98 | 1 |
64 | 5 | |
72 | 3:20 | |
1 | 72 | 10min |
1 | 12 | inf |
Results:
- Amplification of DelG worked, leading to the expected product as well one other unexpected band.
- bands were cut out and DNA purified using QIAquick Gel Extraction Kit
Amplification from FS_08 to FS_11s; 6.5 kb
- Reaction
what | µl |
---|---|
D. acidovorans DSM-39 | 1 |
FS_08: (1/10) | 2 |
FS_11_short: (1/10) | 2 |
Phusion flash Master Mix | 10 |
DMSO | 1 |
dd H2O | 4 |
- Conditions
Biometra TProfessional Basic | ||
---|---|---|
Cycles | temperature [°C] | Time [s] |
1 | 98 | 10 |
14 | 98 | 1 |
62 ↓ 0.5 | 5 | |
72 | 3:20 | |
16 | 98 | 1 |
60 | 5 | |
72 | 3:20 | |
1 | 72 | 10min |
1 | 12 | inf |
23-07-2013
Amplification from FS_08 to FS_23; 6.5 kb
4x 20µl
- Reaction
what | µl |
---|---|
D. acidovorans DSM-39 | 1 |
FS_08: (1/10) | 2 |
FS_23: (1/10) | 2 |
Phusion flash Master Mix | 10 |
DMSO | 1 |
dd H2O | 4 |
- Conditions
Biometra TProfessional Basic | ||
---|---|---|
Cycles | temperature [°C] | Time [s] |
1 | 98 | 10 |
12 | 98 | 1 |
66 ↓ 0.5 | 5 | |
72 | 3:20 | |
18 | 98 | 1 |
64 | 5 | |
72 | 3:20 | |
1 | 72 | 10min |
1 | 12 | inf |
Results:
- Amplification of DelG was successful
- bands were cut out and DNA purified using QIAquick Gel Extraction Kit
- Gel to proof quality of gel extraction was run
26-07-2013
Restriction digest of Fragment FS_08 to FS_23; 6.5 kb; 23-07-2013 with BglII
Incubation at 37°C for 1hour 45min
what | µl |
---|---|
FS_08 to FS_23 cut1 (23-07-2013) | 15 |
BglII | 0.5 |
Buffer 3.1 | 2 |
dd H2O | 2 |
Expected fragment lengths [bp] | 3291, 1936, 1303 |
Results:
- Restriction digest of DelG (FS_08 to FS_23) was successful though one unexpected band (presumably carry over) appeared
- Construct will be further validated by sequencing before potential Gibson Assembly