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  • <p>200 mM</p> <p>100 mM</p>
    24 KB (3,959 words) - 03:44, 22 October 2019
  • ...f palmitic acid (C16:0). These concentrations were 0.4 mM and 1 mM and a 0 mM control<sup>2</sup>. <p>200 mM</p>
    16 KB (2,622 words) - 22:00, 21 October 2019
  • <p>200 mM</p> <p>100 mM</p>
    11 KB (1,663 words) - 22:31, 21 October 2019
  • ...roduce acetone. Both analyses also show the production of approximately 10 mM of ethanol, however this is not a risk factor to the project ethanol is not <li>TYG + 30 mM glucose</li>
    74 KB (9,384 words) - 03:53, 22 October 2019
  • ...00</sub> between 0.6 and 0.8. Next, protein production was induced using 1 mM IPTG followed by additional growth for approximately 7 hours at both 18°C ...rmed into <i>S. cerevisiae</i> and protein production was induced using 1 mM Galactose.
    72 KB (7,937 words) - 14:45, 23 November 2019
  • 100 mM dibasic sodium phosphate (Na<sub>2</sub>HPO<sub>4</sub>) <br> 20 mM KCl <br>
    61 KB (9,653 words) - 03:11, 22 October 2019
  • ...LA-plates containing: chloramphenicol, 1 mM pAzF, 0.2 % arabinose, 0.5 mM IPTG ...LA-plates containing: tetracycline, 1 mM pAzF 0.2 % arabinose, 0.5 mM IPTG
    298 KB (27,610 words) - 18:28, 21 October 2019
  • <p class="text">We used four gradients of TPP (0 mM, 0.1 mM, 1 mM and 10 mM) to test if the addition of TPP may induce cytotoxicity to DE3, and influen ...ntration of TPP, and the DE3 incubated with 1 mM TPP grows best and the 10 mM TPP may significantly inhibit the growth of DE3 cells. But the difference i
    33 KB (3,865 words) - 02:58, 13 December 2019
  • <li>85 mM CaCl<sub>2</sub> + 15% glycerol <li>LB media plus 20 mM Glucose (Add sterile glucose after autoclaving)</ul> <br>
    31 KB (4,992 words) - 14:00, 21 October 2019
  • ...ime (Figure 2). Induction of the system was performed after 165 min with 1 mM IPTG. Overall, the results prove that when expressed, none of our proteins ...fferent inserts. Expression was induced after 165 min of incubation with 1 mM IPTG
    103 KB (11,774 words) - 19:03, 12 December 2019
  • adding EDTA to 10 mM</p> ...e made by diluting the lyophilized oligonucleotides with a 10 mM Tris- 0.1 mM EDTA pH 8.0 solution (TE8.1). Concentrations were checked using a Nanodrop
    309 KB (35,824 words) - 03:46, 22 October 2019
  • ...="c0">10 mM MgCl<sub>2</sub></span></li><li class="c7"><span class="c0">10 mM MgSO<sub>2</sub></span></li></ul><p class="c43"><span class="c0"></span></p
    71 KB (12,145 words) - 03:13, 22 October 2019
  • ...all the mRNA used in this research was generated under the condition of 30 mM GMP. The assay was performed by Agilent Bioanalyzer 2100.</p> ..., MA, USA). An excess amount of GMP was added (7.5 mM, 15 mM, 30 mM to 1.5 mM GTP) to make the in vitro transcripts mono-phosphorylated. After incubation
    46 KB (6,517 words) - 02:29, 14 December 2019
  • ...96 well plate was then performed at glycine concentrations at 50, 1 and 0 mM glycine and reading were taken over 40 hours. The wells were excited at a w ...e. This is because RFP continues to increase for the E. coli treated at 50 mM glycine and the relative fluorescent units are higher when comparing to the
    47 KB (6,702 words) - 01:57, 22 October 2019
  • ...ME_SECONDS:"HH:mm:ss",TIME_MS:"HH:mm:ss.SSS",WEEK:"YYYY-[W]WW",MONTH:"YYYY-MM"},c});
    50 KB (9,776 words) - 02:14, 22 October 2019
  • ...family:Calibri,sans-serif">Control: mini eYFP uninduced and induced with 1 mM IPTG</span></span></span></p> ...FP A+M, mGFP A+C, mGFP O+P in pUltra all samples with and without D-Phe (1 mM)</p>
    424 KB (48,137 words) - 18:36, 13 December 2019
  • ...<ul> <li> Formate concentrations of : 0, 25, 50, 75, and 100 mM </li> </ul> ...<ul><li> Formate concentrations: 0, 15, 20, 30, 50, and 100 mM</li>
    51 KB (5,247 words) - 16:09, 20 October 2019
  • ...s 85.5 mM (low salt), 171 mM (normal LB broth), 256.5 mM, 342 mM and 427.5 mM sodium concentration treatment respectively ...Fluorescence readings were at its peak when sodium concentration were 427 mM.
    31 KB (3,329 words) - 21:09, 21 October 2019
  • <li><span>Buffer P1:</span> 5 mM EDTA, pH 8. Sterilise by autoclaving. Then add RNAse to 300 μg/ml.</li> <li><span>Buffer PE:</span> 10 mM Tris-HCl, pH 8, 80% ethanol. Not sterilised. Prepare in a sterile bottle or
    127 KB (21,654 words) - 03:09, 22 October 2019
  • <td><strong>concentration [mM]</strong></td> <td><strong>concentration [mM]</strong></td>
    68 KB (10,879 words) - 12:23, 13 December 2019

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