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- ...igem.org/Help:Ribosome_Binding_Sites/Mechanism#The_Shine-Dalgarno_Sequence How do bacterial Ribosome Binding Sites work?]== ==[https://parts.igem.org/Ribosome_Binding_Sites/Design How to design an RBS]==4 KB (587 words) - 21:34, 27 May 2013
- how you used this part and how it worked out. ...d to the hairpin loop attached to the ASO+. (For a detailed explanation of how to plan a mammalian transfection <a href= "https://static.igem.org/mediawik16 KB (2,662 words) - 18:21, 1 November 2017
- ==How is the BIOFAB collection useful to you?== ==How do the BIOFAB promoters work?==70 KB (9,598 words) - 04:07, 12 October 2022
- ...o give you '''a brand new Apple iPod or Nintendo Wii!''' (Just think about how fun a Wii would be in lab! :) ...m not very good at Photoshop, so it would be best if some who really knows how to do picture editing touched it up. [http://filer.case.edu/drh19/DNA_Screw12 KB (1,973 words) - 21:13, 27 May 2013
- *[[Help:Sequence_Features|How to Edit and Interpret Part Features]] An overview of the Registry's computational tools and how one may go about using them as they look to design and develop parts, devic6 KB (759 words) - 20:29, 12 July 2017
- Molecular dynamics (MD) simulations are commonly used to see how proteins or other molecules move over time. This can contribute to the unde In our application of forming a hydrogel with ELPs, it can be useful to see how the ELPs will behave at different temperatures. Above a certain transition51 KB (8,206 words) - 13:09, 12 October 2023
- ...only 30 minutes. These results are of particular use as they characterise how long we need to leave bacteria in a particular concentration of IPTG before ...class="italic">Figure 4. Negative control: Fluorescence microscopy showing how RFP expession changes with time on addition of 0mM IPTG in B.subtilis conta18 KB (2,642 words) - 12:50, 26 September 2013
- ===How are these collections curated?=== ===How can users add parts to these collections?===3 KB (503 words) - 16:22, 9 June 2020
- how you used this part and how it worked out. ...ow perform experiments similar to the β-galactosidase assays and evaluate how strong Pveg is in E. Coli. For instance, we can evaluate it and compare wit10 KB (1,555 words) - 00:36, 19 September 2015
- ...astly, a subsection on induction plates for GFP production and determining how fast or slow these senders are communicating with the receiver system Las. ...receiver with these senders. In addition, it allowed our team to determine how fast the senders moved over a certain amount of time with this receiver sys18 KB (2,828 words) - 05:44, 1 November 2017
- <li><b>Aim:</b> to assess how much SUMO-AMP produced in <b>n-time</b> after induction by <b>ammonium in d ...to further <b>reevaluate</b> the inducer system. This also correlates with how much ammonia that is available to be sensed from H. pylori production. <b>I25 KB (3,713 words) - 21:36, 21 October 2021
- How we construct the TMZ-resistance cell line == How we test PDRG1 ==7 KB (1,082 words) - 09:38, 13 October 2022
- ...ation: investigation of the correlation between the different strains and how the varying amounts of salts and sugars in the media stimulate cell growth ...ation was to investigate the correlation between the different strains and how the varying amounts of salts and sugars in the media stimulate cell growth65 KB (10,350 words) - 11:26, 11 October 2023
- ...class="italic">Figure 4. Negative control: Fluorescence microscopy showing how sfGFP expession changes with time on addition of 0mM IPTG in B.subtilis con <td><div class="italic">Figure 5. Fluorescence microscopy showing how sfGFP expession changes with time on addition of 0.05mM IPTG in B.subtilis17 KB (2,405 words) - 00:33, 9 October 2013
- ====How we design our plasmid==== ====How we build our plasmid====10 KB (1,466 words) - 14:53, 12 October 2022
- ...pared LB media stocks for pHs: 4.8, 5, 5.5, 6, 6.6, 7, 7.5, and 8, to test how our plasmids respond to incremental pH changes. We poured 100 mL of liquid ===Experiment 2: Observing how pPink and pTurquoise Function Over Time===7 KB (1,037 words) - 21:05, 10 June 2017
- ...how the protein structure can change with different genetic mutations, and how this contributes to type I, type II, and type III protein S deficiency.<br> ...derstanding of how protein S works, allowing us to create hypotheses about how to affect, control, and modify it. Even in the future, beyond iGEM, knowing13 KB (1,830 words) - 23:56, 13 October 2022
- ...how the protein structure can change with different genetic mutations, and how this contributes to type I, type II, and type III protein S deficiency.<br> ...derstanding of how protein S works, allowing us to create hypotheses about how to affect, control, and modify it. Even in the future, beyond iGEM, knowing18 KB (2,662 words) - 23:14, 11 October 2022
- ...or more details on how we modified ADP1's genome. On this page, we explain how our part collection can be used alongside this two-step protocol to delete ...ACIAD2049 to detect the presence of a Wild-Type <i>nptII</i> gene, showing how ADP1 can be engineered to detect antibiotic resistance.9 KB (1,347 words) - 03:30, 14 October 2022
- how you used this part and how it worked out. Initially, we worked on characterizing how RFP is able to grow independently. Our team wanted to create a standardized27 KB (4,507 words) - 00:42, 21 October 2019