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- Team:Northwestern/protocol/
835 B (136 words) - 18:35, 16 October 2010
- Team:Northwestern/Protocol/PDNA Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]942 B (150 words) - 01:27, 23 October 2010
- Protocol/7
0 B (0 words) - 17:15, 26 October 2010
- Protocol/5
0 B (0 words) - 17:16, 26 October 2010
- Protocol/6
0 B (0 words) - 17:16, 26 October 2010
- Team:USTC/Project/protocol == USTC2010 IGEM DNA Gel extraction protocol == == USTC2010 IGEM Transformation protocol ==1 KB (141 words) - 21:36, 27 October 2010
- Protocol/17
0 B (0 words) - 17:13, 26 October 2010
- Protocol/1
0 B (0 words) - 17:17, 26 October 2010
- Team:Northwestern/Protocol/Quikchange (from primers to colonies! Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]2 KB (393 words) - 01:27, 23 October 2010
- Team:Northwestern/Protocol/Kit to Stock Plasmid Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]3 KB (449 words) - 01:25, 23 October 2010
- Team:Northwestern/Protocol/Ethanol Precipitation ==Procedure: PREFERRED -20°C Protocol== ==Procedure: QUICKER -80°C Protocol==4 KB (639 words) - 01:10, 23 October 2010
- Team:Northwestern/Protocol/New Part Design(PCR) The following protocol is for creating a new biobricks part from a protein coding sequence. Once you have obtained your primers, you can follow the usual PCR protocol using a High Fidelity polymerase. Digest and ligate as usual.2 KB (327 words) - 01:11, 23 October 2010
- Team:Northwestern/Protocol/Transformation Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]1 KB (200 words) - 01:11, 23 October 2010
- Team:Northwestern/Protocol/O/N Culture Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]525 B (92 words) - 01:12, 23 October 2010
- Team:Northwestern/Protocol/Preparation of Competent Cells
2 KB (298 words) - 01:16, 23 October 2010
- Team:Northwestern/Protocol/LB Media Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]218 B (31 words) - 01:19, 23 October 2010
- Team:Northwestern/Protocol/Glycerol Stocks *This protocol describes a method for storing bacterial cultures containing glycerol which Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]]2 KB (323 words) - 01:19, 23 October 2010
- Team:Northwestern/Protocol/Restriction Enzyme Digests Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]] [[Category:Protocol]]982 B (152 words) - 01:20, 23 October 2010
- Team:Northwestern/Protocol/Plasmid Construction ...ning, substantial effort has been put into optimizing the reactions. This protocol describes the exact procedures and quality control techniques used to make Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]]4 KB (585 words) - 01:20, 23 October 2010
- Team:Northwestern/Protocol/3A Assembly ... cell. This issue can be partially checked via the colony PCR step in the protocol though if the genomic DNA is of the same size as your assembly, then the si Back to [[Team:Northwestern/Protocol|<span style="color:#4B088A;">Protocol</span>]]9 KB (1,418 words) - 01:21, 23 October 2010
Page text matches
- Team:Heidelberg/Notebook/BSDesign/July ...B, without Amp); Preperation of competent cells according to the following protocol: * thawing of Huh-7, HeLa p4 and HEK-293 cells according to the following protocol27 KB (3,832 words) - 03:17, 28 October 2010
- 2010.igem.org/Team:Harvard/vectors/notebook <ul><li>Digested O1, O2, E3, E4, R1, R3 with HindIII and SpeI (Fast Digest Protocol - make link)</li> <li>Ran digests on 1% agarose gel (protocol link)</li>20 KB (3,317 words) - 18:23, 22 July 2010
- Team:Johns Hopkins/Notebook ==Protocol== ====Protocol====32 KB (5,044 words) - 03:57, 28 October 2010
- Team:Northwestern/Protocol !align="center"|[[Team:Northwestern/Protocol|<font color="#000000">'''Protocol'''</font>]] [[Team:Northwestern/Protocol/PDNA|Prepping DNA from the kit plates]]5 KB (500 words) - 01:23, 27 October 2010
- Team:Alberta/Building Parts =====Restriction Digest with NotI Protocol:===== =====Ligation Protocol:=====30 KB (4,641 words) - 19:55, 19 August 2010
- Team:Michigan/Oil Sands October ...- following [[Media:Static+biofilm+quantification.pdf|Alex's biofilm assay protocol]] ...ay on pH9 plate, following [[Media:Static+biofilm+quantification.pdf|my protocol]]:15 KB (2,257 words) - 01:08, 27 October 2010
- Team:Yale/Our Project/Notebook/Week 4 <li> Prior to designing thermocycler protocol, used oligocalc to get the following Tm values for the primers. </li> ... annealing temperature of 55˚C. Devised the following "phs" Thermocycler Protocol<br/>21 KB (3,342 words) - 02:50, 28 October 2010
- Team:Michigan/Protocols [[Media:OD600 Cell Dilution Protocol.pdf|OD600 Cell Dilution Protocol]] ...a:Direct Plating Transformation Protocol.pdf|Direct Plating Transformation Protocol]]4 KB (498 words) - 00:01, 27 October 2010
- Team:SDU-Denmark/labnotes9 ''Protocol:'' [[https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1 CP1.1]] <br> ''Protocol:'' [[https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1 CP1.1]] <br>39 KB (5,907 words) - 10:23, 1 October 2010
- Team:SDU-Denmark/labnotes10 '''Protocol:'''[https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.3 CP1.3]<br> '''Protocol:''' [https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1 CP1.1][https://27 KB (4,115 words) - 09:36, 30 September 2010
- Team:SDU-Denmark/protocols ''Protocol'' ...mination of product size. Due to Taq's lack of proofreading, only use this protocol for determining sizes.33 KB (5,192 words) - 03:58, 28 October 2010
- Team:Peking/Notebook/Protocols <html><div id="Protocol Title"> ...rotocols/SDS&WB"><font size=3><font color=#FFFFFF>*SDS-PAGE & western blot protocol</font></font></a> 12 KB (1,933 words) - 05:54, 26 October 2010
- Team:NYMU-Taipei/Experiments/Protocols Follow the protocol based on the kit used. ! Protocol !! GeneArt !! Qiagen !! Viogene9 KB (1,489 words) - 14:23, 27 October 2010
- Team:Michigan/Alex's Notebook ...ved mixture at 121°C for 30 min (sterilize time), following Mike Nelson's protocol Created protocol/plan for experiment. [[Media:Quorum+Sensing+Tables-1-.pdf|Testing AI-2 Res20 KB (3,132 words) - 04:36, 4 October 2010
- Team:KIT-Kyoto/Protocol/Japanese .../Note|Notebook]] > [[Team:KIT-Kyoto/Protocol|Protocol]] > [[Team:KIT-Kyoto/Protocol/Japanese|Japanese]]</td></tr></table> == Protocol ==10 KB (709 words) - 08:58, 9 October 2010
- Team:Michigan/Oil Sands June July *[[Media:6-28-2010_Protocol_for_making_cultures_from_a_-80C_freezer_stock.pdf|Protocol for starting overnight culture from -80°C freezer]] *[[Media:6-29-2010_Making_Frozen_Stoks.pdf|Protocol for making frozen stocks]]13 KB (2,023 words) - 00:19, 27 October 2010
- Team:Lethbridge/Notebook/Lab Work/June ...ollow [[Team:Lethbridge/Notebook/Protocols|competent cell transformation]] protocol to transform the following:<br> ...b> Set up new ligations of pLacI and sRBS-Lum-dT according to Tom Knight's protocol. Previous ligation had very little DNA.<br>76 KB (13,714 words) - 01:36, 25 October 2010
- Team:Heidelberg/Notebook/miMeasure/July *afterwards, RNA Extraction was performed according to the following protocol: '''Protocol'''15 KB (2,038 words) - 00:54, 27 October 2010
- Team:NYMU-Taipei/Experiments/Riboswitch *digest again(because we used XP's protocol for SP) ! PCR Protocol !!34 KB (4,745 words) - 23:56, 27 October 2010
- Team:Michigan/Quorum Sensing ...ved mixture at 121°C for 30 min (sterilize time), following Mike Nelson's protocol *Followed protocol for [[Media:Protocol_Heat_Shock_Transformation_2.pdf|Transformation-heat sh19 KB (2,960 words) - 01:14, 27 October 2010
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