................................................
The result of the PCRs was analyzed on a 1% agarose gel, run for 1 h @ 100 V (Gel1).
As the result of the first pSB vector PCRs was not ideal due to strong side products, the PCR was repeated in 6 replicates according to the following protocol:
25 ul Phusion PCR MasterMix
1 ul template DNA (pSB1C3, digested with PstI/EcoRI/DpnI)
0.5 ul of each primer SB-prep-3p/SB-prep-2Ea
add water to final volume of 50 ul
The 2.1 kb band was afterwards cut out from the gel and a gel extraction was applied for purification of the DNA (Qiagen Gel Extraction Kit).
PCR was performed, applying the standard protocol (annealing temperature 60 °C).
5 ul of PCR product were analyzed on an agarose gel, run for 1 h @ 100 V.
22/08/2010
Fusion-PCR for the construction of the whole RSV promoter fragment with BBB prefix and suffix:
1 ul (50 ng) of RSV5' template (or RSV5' (reverse complementary))
1 ul (10 ng) of RSV3' template (or RSV3' (reverse complementary))
10 ul buffer
1 ul Hifi Polymerase (2.5 u)
36 ul water
The PCR was performed according to the following protocol:
................................................
PCR for the construction of linear vector, the PCR was further optimized by applying again the Hifi and the Phusion PCR protocol from the previous day, but using an annealing temperature of 64 °C that time.
The PCR for both fragments was analyzed on a 1 % agarose gel, run for 1 h @100 V (Gel1) and PCR purified applying a Qiagen PCR purification Kit.
Digestion of PCR product and Vectors
1 ug of each vector PCR and insert PCR product was digested with EcoRI/PstI according to the NEB standard digestion protocol (10 u Enzyme, final volume 50 ul).
After heat inactivation (20 min @ 80 °C), 2 ul (2 u) of shrimp acidic phosphatase were added to the vector digestions and incubated for 30 min @ 37 °C. After the digestion, a purification was performed using a Qiagen PCR purification kit.
Ligation
Ligations were set up using the Fermentase Ligation Kit. The following vector and insert ratios were used:
Vector 1 (Gel Extracted from previous day) and vector 3 (Phusion PCR product, PCR purified); 4 ul (40 ng):
Furthermore, negative controls were set up for each vector.
Transformation in E. coli Top10 cells were performed according to the standard transformation protocol.
23/08/2010
gel1
Gel2
Colony-PCR of the colonies obtained on the agar-plates (cloning previous day) was performed according to the following protocol:
12.5 ul Phusion MasterMix
0.25 ul of each primer
12 ul of water
colony picked from agar-plate
2 colonies were picked for each construct.
The PCR was performed according to the standard Phusion PCR protocol.
In parallel, a MiniPrep Culture for each colony was inocculated.
PCR for the construction of Luc2, hRluc, CMV, SV40 promoter, SV40 terminator and the BGH-Terminator. Therefor, PCR reactions were set up according to the following protocol:
10 ul Hifi Buffer
0.5 ul of each primer
1 ul (50 ng) of each template
38 ul of water
The combination of templetes and primers were as follows for the mentioned constructs:
PCR was performed according to the standard Hifi-Protocol (annealing temperature 57 °C)
Gel2
24/08/2010
Gel1
Gel2
Gel3
Amplification of the CMV Promoter as well as the amplification of pSB1A3/C3/K3 standard plasmid backbones was performed via Phusion or Hifi-PCR according to the standard protocol (annealing temperature 61 °C).
The PCR product was run on a Gel for 1 h @ 100 V and analyzed an a 1 % agarose gel (gel 1).
Another colony-PCR of the colonies obtained on the agar-plates (cloning two days before) was performed according to the following protocol:
12.5 ul Phusion MasterMix
0.25 ul of each primer
12 ul of water
colony picked from agar-plate
Two colonies each were picked from plate (1) and (2) and four colonies of plate (3) for each construct, respectively.
The PCR was performed according to the standard Phusion PCR protocol.
In parallel, a MiniPrep Culture for each colony was inocculated.
The result of the colony-PCR was analyzed on a 1 % agarose gel, run for 1 h @ 100 V (gel2).
a PCR for the construction of synthetic microRNAs and microRNA binding sites was perfomed. For the construction of binding sites, single stranded oligos were ordered and second strand synthesis was performed using the BBB_suffix_reverse primer. The protocol was as follows:
1 ul microRNA binding site oligo
0.5 ul BBB_suffix_reverse primer
23.5 ul water
25 ul Phusion MasterMix
The binding site oligos for the following microRNA binding sites were used:
hsa-miR-375 (perfect, 9-12 mut, 9-22 mut)
hsa-miR-376a (perfect, 9-12 mut, 9-22 mut)
hsa-miR-122 (perfect, 9-12 mut, 9-22 mut)
shRNA-6 (perfect, 9-12 mut, 9-22 mut)
shRNA-7 (perfect, 9-12 mut, 9-22 mut)
shRNA-8 (perfect, 9-12 mut, 9-22 mut)
shRNA-9 (perfect, 9-12 mut, 9-22 mut)
shRNA-10 (perfect, 9-12 mut, 9-22 mut)
PCR for the construction of synthetic shRNAs was performed. Therefore, the pcDNA5/TO/FRT containing the shRNA miRsAg as insert was used as template. For the shRNAs 1,2,3,5,6,7,8,9,10 the synthesis of two intermediate fragments were performed. The 5' fragment was amplified by using the primer shRNA_AflI_BBb_fw and the reverse oligos of the certain shRNA gene. The 3' framents were amplified by using the primer shRNA_HindIII_BBb_rev and the forward primer of the certain shRNA gene. The forward and reverse primer of the shRNA gene introduce the guiding and passanger with certain specificities into the shRNA constuct. The miRsAg is an miR-122 like shRNA and uses the backbone of miR-122, but another guiding and passanger strand. The PCR was set up according to the standard protocol (annealing temperature: 58 °C).
The results of the PCR were analyzed on a 2 % agarose gel, run for 30 min @ 100 V (gel 3)).
25/08/2010
The constructs were tested in a digestion with NotI using the following protocol:
4.0 ul template
2.5 ul NEB buffer 3
2.5 ul BSA
0.5 ul NotI (NEB)
add 25 ul
For RSV, RSV(reverse complementary), BGH(forward) und SV40 promoter (reverse complementary) positives bands were found and samples were send for sequencing.
Cloning of constructs BBb_CMV, Luc2_ter, hRluc, sv40(forward) and BHG(forward):
Digestion of pSB1C3 and the PCR products of the mentioned constructs with EcoRI/PstI (1 ug each) according to the standard digestion protocol.
Subsequent purification using a nucleaotide removal kit and ligation overnight at 16 °C.
26/08/2010
The sequencing result for the samples send for sequencing on the privious day was checked. The results were positive for all samples, sequences were accurate.
Transformation of the ligation done on the previous day according to the standard transformation protocol.
27/08/2010
gel1
gel2
PCR was carried out for the following parts, using the standard HiFi protocol:
1. Backbone amplification using primers backbone_AvrII_fw and backbone_AvrII_rev
Colony PCR was carried out (according to the standard PhusionMix protocol, annealing temp. 57 C) for CMV, Luc2, hRluc, SV40, SV40 ter and BGH-1 rc. Only one sample for hRluc and one for SV40 ter showed a possible positive result (gel1).
The three standard plasmids (pBS_1A3, pBS_1C3, pBS_1K3) were digested with EcoRI and PstI according to the following protocol:
5 ul of each plasmid (conc. = ?)
3 ul EcoRI buffer
3 ul BSA
0.5 ul of each enzyme
18 ul nuclease-free water
Incubatation: 37 C, 1hr
Heat inactivation: 80 C, 20 min
Then DpnI was added (0.5 ul), and the tubes were incubated at 37 C for 1 hr, then heat-inactivation at 80 C for 20 min.
5 ul of the product were loaded on a 1% agarose gel and analyzed (gel1).
28/08/2010
6 more colonies from the cloning done on the 25th/26th were picked and colony PCR was performed according to the standard colony-PCR protocol. In parallel, Minipreps of each colony were inocculated. The results of the colony-PCR ist shown in the gelpictures.
shRNA construction via PCR; Template: 50 ng of first PCR product; Standard PCR protocol using an annealing temperature of 60 °C.
29/08/2010
gel1
gel2
Vector pcDNA_BBbCMV, PCR product Luc2_ter and shRNA(1-10) with EcoRI/PstI (1 ug each). The BBb_CMV was cut out from the gel (~ 700 bp band) and gel purified (gel1). The PCR product Luc2_ter was purified by applying a nucleotide removal kit.
Ligation reactions were set up using pSB1C3 (amplified using Phusion HF Mastermix (1) or High Fidelity Polymerase (2) cut EcoRI/PstI) (100 ng) and 100 ng CMV, 40 ng shRNA or 300 ng Luc2 constructs. For shRNA6 and CMV the cloning was done in 2 replicates (using either the pSB1C3 amplified via HF Mastermix or High Fidelity Qiagen Kit). The ligation was performed according to the fermentas ligation kit protocol and incubated for 1 h @ room temperature. Afterwards, 10 ul were transformed into Top10 cells.
30/08/2010
Gel1
Gel2
Gel3
The ligation result from the previous days' cloning was analyzed via colony PCR (gel 1-3) and all colonies were inocculated (LB cultures) The construct numbers indicate the number of the clone picked from the agar plate. If cloning was performed in Replicates, the first number indicates the plate (i.e. CMV3) and the second number the clone. As seen in gelpicture 1 the clone CMV3.1 and on gelpicture 3 the clones CMV 2,3,12 and 16 all show the right band length of ~1000 bp. On gelpicture 2 the shRNA10.1 clone shows the right band as well as the Luc2.1.5 clone for the Luc2 luciferase.
31/08/2010
Gel1
Gel2
The LB cultures from the previous day were inocculated and mini prepped. Afterward, a test digestion of all constructs with NotI was performed (gel1) and loaded on a 1 % agarose gel run for 35 min @ 100 V. The samples CMV2, CMV3 (23), CMV3.1, Luc2.1 and sh10.1 showed the right bands on the gel and samples were send for sequencing. All sequencing results showed, that the constructs were right.
pSMB_Measure backbone (igem team HD 2009 measruement standard) was amplified using the ClaI/XhoI or AvrII primers and performing a standard Phusion HF Mastermix PCR protocol (annealing temperature 61 °C. The PCR result was loaded on the agarose gel 1 for control (BcA = AvrII cutting sites, BcB = XhoI/ClaI cutting sites). The PCR products of the used vectors pSB1C3 and the hRluc and Luc2 PCR fragments used in this and subsequent clonings was also loaded on the gel for controlling purposes.
Digestion of the pSB1C3 vector amplified via Phusion HF PCR Mastermix (annealing temperature 61 °C) with EcoRI/PstI for 1 h @ 37 °C. After heat inactivation, 1 ul of DpnI was added to the restriction mix an digestion performed for another hour. The product was SAP (dephosphorylation) or not SAP treated this time. Furthermore, the hRluc, Luc2, CMV_TetO2, sv40 and FRT site PCR products (see 08/27/2010) were digested EcoRI/PstI as well.
Ligation: each PCR fragment was ligated into digested vector backbone pSB1C3. 50 ng of the non-treated and 100 ng of SAP treated vector were used in the ligation reactions. Amount of insert was calculated to be 2 fold (large fragment Luc2 and hRluc) or 3-5 fold of the molar vector amount. Ligation was performed for 1.5 h @ room temperature. The ligation was analyzed on a 1 % agarose gel, run for 35 min @ 100 V. The non-treated vector is indicated via number 1 (i.e. Luc2.1) the SAP-treated vector with nr. 2 (i.e. Luc2.2). As control, the digested insert fragment PCR products and digested vectors were loaded on the gel as well. For hRluc, Luc2 and CMV_TetO2 correct product bands are clearly visible. For sv40, that is not the case. The FRT site is to short, to be able to distinguish clearly between vector fragment and ligated Vector with Insert. Subsequently, a transformation of all 10 ligation reactions into Top10 cells was performed according to the standard transformation protocol.
8 colonies of each plate (see previous day) were picked and colony-PCR was performed. Furthermore, the colonies were used for inocculation of LB miniprep cultures. The numbers behind the construct name refer to vector type (1 = not SAP treated, 2 = dephosphorylated using SAP; see previous day). For hRluc (1300 bp band)), Luc2 (2300 bp band), CMV_TetO (1000 bp band) and the FRT (500 bp band) site, positive colonies could be observed (gel 100901-1 and 100901-2).
PCR for the construction of the standardized Tet Repressor was performed. The PCR was set up using the Phusion HF MasterMix and standard PCR protocol was applied (annealing temperature 59 °C, 2 replicates). The result of the PCR was analyzed on a 1 % agarose gel (gel 100901-2, lower right side) and the right 700 bp band was clearly visible.
Digestion of the TetR fragment with EcoRI/PstI was performed according to the standard digestion protocol and the fragment was subsequently ligated into pSB1C3 (SAP treated or non-treated). The ligation mix was transformed into Top10 cells.
02/09/2010
Gel 100902-1
8 colonies were picked from plates 1 and 4 colonies from plates 2 from the previous days cloning and analyzed via colony PCR performed according to the PCR standard protocol. The results of the colony PCR were analyzed on a 1 % agarose gel run for 1 h @ 100 V (gel 100902-1 and 100902-2). The following colonies were afterwards inocculated (LB miniprep cultures):
TetR (1.4 and 1.6)
shRNA6 (1.1, 1.4 and 1.8)
shRNA7 (1.1, 1.5 and 1.6)
shRNA8 (1.1, 1,2, 1,3)
shRNA9 (1.2)
The cultures inocculated the day before were mini prepped by applying a Qiagen Miniprep Kit. Afterwards, a test digestion with NotI was performed and the result was analyzed on a 1 % agarose gel, run for 35 min @ 100 V (gel 100902-3). According to the test digestion result, the following samples were send for sequencing @ GATC:
CMV_TetO2 (.4, 1.6)
FRT (1.1, 1.3)
Luc2 (1.4, 1.6)
hRluc (1.1, 1.3, 1.4)
Gel 100902-2
Gel 100902-3
03/09/2010
Gel 100903-1
Gel 100903-2
Test digestion with NotI of the cloned constructs on the previous day (gel 100903-1). For the TetR constructs the expected 600 bp band and for the shRNA constructs, the expected 200 bp band were clearly visible. For each construct, one sample was send for sequencing. Sequencing results were correct for all samples send for sequencing.
Purification of single binding sites against shRNA6-10, miR-375/376/122. For each target, the perfect, 9-12 and 9-22 randomized binding sites were purified and analyzed on an agarose gel (100903-2). All bands were clean, with just a slight amount of side product for the 9-22 randomized binding sites.
05/09/2010
transformation of final Kit constructs F1 - F16 into E. coli Top10 cells
06/09/2010
inocculation of miniprep LB cultures for the constructs F1 - F16 from single colonies from the plates prepared the previous day
digestion of PCR amplified vector backbone pSB1A3 with EcoRI/PstI; after subsequent heat inactivation, digestion with DpnI was performed and the vector was purified by applying a nucleotide removal kit.
07/09/2010
Gel 100907-1: Ligation Control. Numbers indicate the F-Construct numbers of the parts assembled
Miniprep of constructs F1 - F16 using a Qiagen Miniprep Kit
Digestion of 500 ng of each construct with the following enzymes
F2, F3, F5 with EcoRI/NheI
F8, F1, F15, F11, F12, F13, F14, F7 with PstI/SpeI
Ligation of the follwing constructs into pSB1A3 via standard 3A assembly
Digestion of 500 ng F6 with XbaI; purification via nucleotide romoval kit
Annealing of XbaI mutation oligo according to the following protocol
prepare mixtrure of oligos (5 ul @ 100 mM each) in NEB buffer 2 (volume 50 ul)
heat up to 95 °C in heating block; cool down to room temperature slowly
incubate on ice for 10 min
0.5, 1 and 3 ul of the annealed oligos were then ligated into 50 ng of pre-digested F6 construct;
All Ligations were controlled by loading 10 ul of ligation reactiong onto a 1 % agarose gel (100907-1), run for 35 min @ 100 V
08/09/2010
Gel 100908-1: Colony-PCR.
Colony PCR of the previous days' cloning and miniprep cultures were inocculated in parallel; The result of the PCR was analyzed on a 1 % agarsoe gel (100908-1) run for 35 min @ 100 V.
09/09/2010
Gel 100909-1
Gel 100909-2
Miniprep of the cultures inocculated on the previous day followed by test digestion of 300 ng of each constructs with NotI (gel 100909-1). The positive samples were send for sequencing @ GATC. The gel looks weird due to use of 0.05 x TAE buffer instead of 0.5 x.
The nine Luc2-SV40 constructs were with XbaI and NheI (negative testing), and XhoI and PstI (positive testing) for the induced mutation. The reaction was set up according to the standard protocol, and then the samples were visualized on a 1% agarose gel (gel 100909-2).
10/09/2010
PCR of SV40 Terminator with BamHI site according to standard PCR protocol (annealing @ 58 °C)
Assembly of the following constructs, again via 3A standard assembly.
F6/F1, F6/F8, F10/F4, F5/F1, F16/SV40, F5/F8
Subsequent Transformation into DH5alpha cells
11/09/2010
Gel 100911-1
Gel 100911-2
Colonies were picked from the plates from the previous days' cloning and a colony PCR was performed according to the standard protocol. In parallel LB miniprep cultures were inocculated for each colony (gel 100911-1 and 100911-2).
12/09/2010
Gel 100912-1
Gel 100912-2
Minipreps were done by applying a Qiagen Miniprep Kit for the positive candidates picked on the previous day. Test digestion was performed by digesting ~ 250 ng of each construct with SpeI/NheI and the result was analyzed on a 1 % agarose gel (100912-1 and100912-2) run for 40 min @ 100 V. For all the constructs we got the right band despite construct F10/F4.3. Positive constructs were send for sequencing @ GATC.
ligation of the following parts (50 ng of vector, equal amounts of parts)
F4/F5 into pSB1A3 (precut E/P)
R5 with either R1, R2, R3 or R4 into pSB1C3 (precut E/P)
R6 with either R1, R2, R3 or R4 into pSB1C3 (precut E/P)
R9 into pSB1C3 (precut E/P)
R10 into pSB1C3 (precut E/P)
transformation of 10 ul ligation reaction after heat inactivation into DH5alpha cells
14/09/2010
Gel 100914-1
Gel 100914-2
Colony- PCR for the cloning products done on the previous day (gels 100914-1 and 100914-2 on the right)
positive clones were Mini-Prepped and test digested
15/09/2010
Gel 100915-1
PCR for the introduction of the Kozag-Sequence in front of the hRluc_BGH part; two strategies were performed in parallel using different touchdown-PCR protocols. Protocol nr. 1 was set up as follows:
25 ul Phusion HF MasterMix
0.5 ul of 100 um primers
1 ul of template R12 (50 ng/ul)
23 ul of water
Touchdown PCR was performed according to the following protocol:
................................................
95 °C/5 min
................................................ (1x)
95 °C/30 s
68 °C/45 s (- 0.5 °C/cycle)
72 °C/1 min
................................................ (35x)
72 °C/10 min
................................................ (1x)
4 °C/ forever
................................................
Protocol nr. 2 was set up as follows:
25 ul Phusion HF MasterMix
0.1 ul of 100 um primers
1 ul of template R12 (50 ng/ul)
23.8 ul of water
Touchdown PCR was performed according to the following protocol:
................................................
95 °C/5 min
................................................ (1x
95 °C/15 s
68 °C/45 s (- 0.5 °C/cycle)
72 °C/1 min
................................................ (15x)
95 °C/15 s
60 °C/30 s
72 °C/1 min
................................................ (20x)
72 °C/10 min
................................................ (1x)
4 °C/ forever
................................................
Each PCR was performed in two replicates. The result of the PCRs was analyzed on a 1 % agarose gel (100915-1), run for 1 h @ 100 V. The PCR nr. 2 was subsequently PCR purified by applying a Qiagen PCR purification KIT and used for the cloning
16/09/2010
Cloning of Kozag_hRluc_BGH fragment into pSB1C3 and Constructs R24-R31
Cloning of the XhoI/XmaI_suffix oligo via NheI/PstI into the TetR construct F16)
Digestion of PCR fragment with SpeI/PstI according to 3A standard protocol; digestion of destination Vector pSB1C3
Ligation and Transformation were done according to the standard protocol
17/09/2010
Gel 100917-1
Gel 100917-2
Selection of colonies from the plates (see previous days' cloning) via colony-PCR using the standard sequencing primers; a ~5.5 kb fragment should be visible for the assembled construct K1-K8, if colony-PCR was positive (gel 100917-1 and 100917-2). No sample shows a 5.5 kb band, but that's most likely due to the very difficult amplification of such a long fragment with Fermentas 2x PCR MasterMix (Taq-based). Therefor 3 miniprep cultures were inocculated for each construct (K1-K8). The TetR oligo insertion and the Kozag_hRluc_BGH cloning into pSB1C3 gave the right bands on the gel.
19/09/2010
Miniprep of the previous days inocculated miniprep cultures
20/09/2010
Gel 100920-1
Gel 100920-2
test digestion of the miniprepped clones (previous day) with EcoRI/PstI; For all clones at least 2 digestions gave the exactly expected band (gel 100920-1 and 100920-2); therefor we can say, that the tuning construct is succesfully assembled and ready to be tested
21/09/2010
22/09/2010
digestion of R23 with EcoRI and PstI in EcoRI Buffer (NEB) and ligation into digested Template:Part, transformation, growing on selective agar plates (chloramphenicol), following standard protocol recommendations
23/09/2010
Gel 100923-1. Analytical gel with following lanes: 1) till 8) colony PCR products with nice bands as expected at ~ 800 bp especially at lane 1, 4, 6 and 8, lane 9) 1kb Plus Ladder (Invitrogen)
"Something is rotten in the state of Genemark..." Lorenz 18:00, 24 September 2010 (UTC)
inoculation and colony PCR of the transformed (23A+33A)=56C construct from yesterday. Same PCR protocol was used, even though the fragment should be 1100 and therefore elongation was probably not long enough. The PCR showed a band at 300bp, which dominik says is normal if you have religated vector. But nevertheless, miniprep of La1, La3 and La4 were made, because they didn't show a strong negative PCR band.
test digestions (actually they are preparative, the only difference is I will test them on the gel as well to be sure I have the right thing)
R23A from yesterday (miniprep 8 and 8/) is digested with Eco&Nhe, expected fragment is 500bp
R33 with Spe&Pst, expected fragment 600bp
R56C with Spe&Pst, expected fragment 1100bp
R8 with Eco&Nhe, expected frament 1000bp
ligation of R23A+R33+backbone C
ligation of R56C + R8 + backbone A
25/09/2010
PCR amplification of standardised pcDNA5 p55 and p1 with primer D47/48 and D55/69
26/09/2010
Gel 100926-1. Analytical gel with following lanes: 1) R33 E/N (from 23rd September) 2) R23_1 S/P 3) R23_6 4) R33C 5) R23_4 6) R23_8 7) 1kb Plus Ladder (Invitrogen) 8) R33C E/N 9) R23_4 S/P 9) R23C_8 S/P
Gel 100926-2. PCR results of p55 and p1: p1 with primer 47/48 (lane 1), p1 with primer 55/70 (lane 2), p55 with primer 47/48 (lane3), p55 with primer 55/70
miniprep of R23C cultures again (colonies from transformation (done on wednesday))
check of all digestions on an analytical gel (see gel 100926-1)
fragment for R23_6 is a bit smaller than expected (rather 400 bp than 500 bp)
originally digested R23A runs slightly below 500 bp, too (data not shown)
because of reverse elements and resulting secondary structure?
repetition of ligation with R23_6 and old R33 (nice band at roughly 600bp)
including negative control at this time with only backbone Template:Part
gel extraction of PCR on p55 and p1 (see gel 100926-2)
recloning of R1,R4 and R7 into standardbackbone Template:Part
digest 500ng of R1, R4 and R7 with EcoRI and PstI
heat inactivate 20 min at 80°C
Nucleotide removal
ligate 150ng and 250ng of insert into 30ng Template:Part 1h at RT and transform ligation
27/09/2010
Gel 100927-1: colony PCR on K1 (lane 1-8), K4 (lane 9-16) and K8 (lane 17-24)
Gel 100927-2: colony PCR K1 (lane 1&2), K4 (3&4) und K7 (5&6), K3 digested with BamHI (7), K3 digested NheI and SpeI (8), R33 in pSB1A3 digested with EcoRI and PstI (9), R33 digested with NheI and SpeI (10)
tuning construct:
colony-PCR on K1, K4 and K7 cloned into Template:Part showed nearly only positives as a band of 400bp is expected by using the primer pair 50/75
analysis of transformations from yesterday (i. e. (R23+R33) + R8 or (R23+R33) + R11 in chloramphenicol standard backbone)
only re-ligations (as assumed from negative control), more colonies next day
29/09/2010
Gel 100929-1 first gel: double digestion of K1 and K3 with PstI and EcoRI: K1 (lane 1-4), K3 (lane 5-8), second gel: digestion of K1 and K3 with BamHI: K1 (lane 1-4), K3 (lane 5-8)
Gel 1000929-2 digestion of K1 and K3 with HindIII and AflII: K1 (lane 1&2), K3(lane 3-12)
gel 100929-3 pcr on binding sites for shRNA 10
tuning construct:
mini Prep on K3 and K1 constructs
test digestion with PstI & EcoRI and BamHI showed all positive results
digest K3 and K1 with HindIII and AflII
cloning of shRNA 6 and 7 into K1, K3, K4 and K7:
colony PCR on ligation from the 28/09/2010 did not reveal any positives by using the following protocol:
colony PCR on ligations from the 28/09/2010 did not reveal any positives by using the following protocol:
start from the beginning again: in doublicates:
first procedure:
digest PCR on shRNA 6 and 7 as well as K1, K3, K4 and K7 with HindIII and AflII
purify shRNAs with nucleotide removal kit
purify digested K3 and K1 with gel extraction kit
ligate K1, K3, K4 and K7 with shRNA 6 and 7
second procedure:
digest K4 and K1 as well as shRNA6 and 7 from PCR product and purify via nucleotide removal kit
ligate K4 and K3 with shRNA 6 and 7
transform all ligations
cloning of binding sites:
second strand synthesis PCR on binding sites for shRNA 10
Gel 100929 r-4: colony PCR of repressor construct, band at 350bp points at backbone religation.
Gel 100929 r-5: test digestion of miniprep number 14 withe EcoRI and NheI shows expected band at 1100bp. Digestions of R8 and R11 were also positive, DNA cut out with SpeI and PstI runs at 800bp. Lane 1=miniprep 14 undigested, lane2=miniprep 14 digested, lane3=miniprep 23 digested, lane4=R8 undigested, lane5= R8 digested, lane6=R11 undigested, lane7=R11 digested
repressor construct:
colony PCR after transformation of P56+R8 and P56+R11 (P56=R23A+R33) yielded no positive results
miniprep of colonies 11, 14, 17 and 23 from P56 cloning were repeted because of bad miniprep results yesterday, then digested with S/P
R8 and R11 were digested with E/N again
digestion of P56 colony 14 was positive on the gel, digestion of R8 and R11 also gave the right fragments
pBS 1C3 backbone was [http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_ef0511.pdf SAP] treated to reduce religation that was likely to be the problem with previous transformations
ligation of P56 (14) with R8 and R11 and SAPed backbone and control ligation with backbone only, transformation
30/09/2010
Gel 1000903-2 colony PCR on shRNA10 cloned into K3 and K4
Gel 1000930-3 colony PCR on shRNA10 into K3 and K4
tuning construct:
colony pcr on shRNA 6 and 7 into construct K3 and K4
cloning of binding sites for shRNA 10 into K3 and K4:
digestion of binding sites (perfect, imperfect 9-12 and imperfect 9-22) for shRNA10 with xhoI and ageI :) and construct K3 and K4 in psB1A3 with xmaI and xhoI
ligation of binding sites with digested constructs
transformation of ligation into TOP10 cells
plate on ampicillin plates ON
Gel 100930-1 colony PCR of Repressor construct with different promoters (R8 or R11). Positive colonies show an amplification product at 2500bp (lanes 1,2,4-8, 10, 13-16)
plenty of colonies on the P56+R8 and P56+R11, NO colonies on control plate with SAPed backbone, colony PCR revealed 50% of positive clones
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