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authorBonface2024-02-13 23:52:26 -0600
committerMunyoki Kilyungi2024-08-09 13:30:43 +0300
commitb2feda451ccfbeaed02dce9088d6dd228cf15861 (patch)
tree3dd2883524985114070a7770cd2e9f9bd7eb1848 /general/datasets/DoDTATRCRetExMoGene2_0315/tissue.rtf
parentd029d5d7f8ead1f1de8d318045004a4a6f68f5fb (diff)
downloadgn-docs-b2feda451ccfbeaed02dce9088d6dd228cf15861.tar.gz
Update dataset RTF Files.
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-<p>Tissue preparation protocol. Animal were killed by rapid cervical dislocation. Retinas were removed immediately and placed in 1 ml of 160 U/ml Ribolock for 1 min at room temperature. Dissecting and preparing eyes for RNA extraction Retinas for RNA removed from the eye and placed in Hank&rsquo;s Balanced Salt solution with RiboLock (Thermo Scientific RiboLock RNase #EO0381 40U/&micro;l 2500U) and processed per manufacturer&rsquo;s instructions (in brief form below).</p>
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-<p>1) Sample collection for RNA isolation.</p>
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-<p>2) Quickly remove the retinas with clean curved forceps after cervical dislocation of the mouse.</p>
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-<p>3) Put each retina in 1 ml of 160 U/ml Ribolock for 1 min in RT.</p>
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-<p>4) Move the retina to another tube with 50&micro;l Ribolock, store in -80&deg;C.</p>
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-<p>5) The RNA was isolated using a QiaCube and the in column DNAse procedure.</p>
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-<p>Quality Control: All RNA samples were checked for quality before running microarrays. The samples were analyzed using the Agilent 2100 Bioanalyzer. The RNA integrity values for each sample are presented in Table 1 below.</p>