{"Equipment":"<p>Celeris - Diagnosys LLC</p>","Procedure":"<h2>Procedure</h2> <ol>    <li>Transfer mice from the animal room to the testing room.</li>    <li>       Mice are dark adapted overnight (alternatively: minimum of 2 hours) for testing procedures.              <ol style=\"list-style-type:lower-alpha;\">          <li>All rod testing procedures are done under dim red light after a minimum 2-hour dark adaptation period</li>          </li>       </ol>    <li>Following dark adaptation one drop of an appropriate mydriatic solution is applied to each eye to induce pupil dilation.</li>    <li>Once the pupils have dilated mice are anesthetized with the inhalation of 2% Isoflurane.</li>    <li>When the mouse has reached the proper plane of anesthesia, the mouse is placed on a heated platform and the nose is placed in the nose cone for continuous anesthetic inhalation.</li>    <li>An appropriate opthalmic lubricant is applied to the electrodes before placing on each cornea.</li>    <li>The scotopic test is performed with pulsing white light.</li>    <li>A 3-minute light-adaptation follows before the photopic test is run. At this time an additional drop of opthalmic lubricant should be added to each eye without adjusting the electrodes.</li>    <li>After 3 minutes of light adaptation, photopic ERGs are obtained with brighter white flashes at varying stimulation intensities.</li>    <li>Once the photopic test is complete, carefully remove the recording electrodes and apply a generous amount of an ophthalmic gel to both eyes and allow the mouse to recover in a clean heated pen until fully conscious.</li>    <li>Return the mouse to its home pen.</li>    <li>Clean the electrodes with sterile water followed by 70% ethanol.</li>    <li>Save the test results and export to the server.</li> </ol>","Purpose":"<p> Full-field electroretinogram (ERG) is a mass electrical response of the retina to a light stimulus. The ERG contains four components: a-wave, b-wave, c-wave and FO-wave.  These four components reflect the responsiveness of retinal photoreceptor cells and other neurons as a measure of visual function.</p>","Experimental Design":"<div class=\"expandable\">\r\n<ul>\r\n<li><strong>Minimum number of animals :</strong>&nbsp;<impress:lookup>procedure.minAnimals</impress:lookup></li>\r\n<li><strong>Age at test: </strong>Week 15</li>\r\n<li><strong>Sex:</strong> We do not expect the results of this test to show sexual dimorphism</li>\r\n</ul>\r\n</div>\r\n<p>&nbsp;</p>","Notes":"<p>Amplitude and timing measures of the ERG waveform are taken:</p><ol>\t<li>The a-wave amplitude is measured from the pre-stimulus baseline to the lowest negative trough; the b-wave amplitude is measured from the trough of the a-wave to the following highest peak; the c-wave amplitude is measured from the pre-stimulus baseline to the following highest peak; the FO- wave amplitude is measured from the peak of the c-wave to the subsequent lowest trough.</li> <li>Implicit time (t) is measured from stimulus onset to the trough or peak of each wave.</li></ol>"}