Difference between revisions of "Part:BBa K1033916:Experience"
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<table cellpadding="2" border="1px" cellspacing="0" align="center" width="70%"> | <table cellpadding="2" border="1px" cellspacing="0" align="center" width="70%"> | ||
− | + | <td><b>Measurement Type</b></td> | |
− | < | + | |
− | + | ||
− | + | ||
− | + | ||
<td>Fluorescence</td> | <td>Fluorescence</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Microplate name</td> | + | <td><b>Microplate name</b></td> |
<td>COSTAR 96</td> | <td>COSTAR 96</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Scan mode</td> | + | <td><b>Scan mode</b></td> |
<td>orbital averaging</td> | <td>orbital averaging</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Scan diameter [nm]</td> | + | <td><b>Scan diameter [nm]</b></td> |
<td>3</td> | <td>3</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Excitation</td> | + | <td><b>Excitation</b></td> |
<td>470-15</td> | <td>470-15</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Emission</td> | + | <td><b>Emission</b></td> |
<td>515-20</td> | <td>515-20</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Dichronic filter </td> | + | <td><b>Dichronic filter </b></td> |
<td>auto 491.2</td> | <td>auto 491.2</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Gain </td> | + | <td><b>Gain </b></td> |
<td>500</td> | <td>500</td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>Focal height [nm]</td> | + | <td><b>Focal height [nm]</b></td> |
<td>9</td> | <td>9</td> | ||
</tr> | </tr> |
Revision as of 17:42, 26 August 2017
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Applications of BBa_K1033916
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UNIQ0a3795cfe7155acf-partinfo-00000000-QINU UNIQ0a3795cfe7155acf-partinfo-00000001-QINU
•••••
Hong Kong-CUHK iGEM 2017 |
Fluorescent properties of amajLime Although amajLime is described as chromoprotein in main page, we characterised its spectral properties and found the max excitation and emission wavelength at 445 nm nd 485 nm respectively.
We transformed part BBa_K1033916 with constituitive promoter: J23100 in C41 and grew in 2XYT for 24 hours. Purifying the amajLime by Ion Exchange Chromatography and Hydrophobic Interaction Chromatography, we measured the fluoresece of purified amajLime, which is diluted to 10µg/100µl (total 200µl) in triplicates, in different buffers (ranges from pH2 to pH12). The result shows that the stability drops dramatically in condition below 6 and attains maxima fluorescence at pH 8. |