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    <responseDate>2026-10-14T20:19:42Z</responseDate>
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    <identifier>10.57760/sciencedb.03353</identifier>
    <datestamp>2022-10-12T14:01:14Z</datestamp>
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  <dc:date>2022-10-12</dc:date>
  <dc:title>chip-seq data  of C57 mouse spleen derived CD8+ T cells lactate/lithium carbonate treated with lactylated</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.03353</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>The data used CD8+T cells from C57 mouse spleen. After being activated by CD3/28, they were treated with 10mM lactic acid and 1mM lithium carbonate for 24 hours respectively. The cells were fixed, and protein and gene location information were stabilized after cross-linking. Chip seq was used to analyze the histone gene sites modified by pan Kla. They are divided into the following four groups:; 1. The control group (CTR) was solvent control; 2. The lactic acid treatment group (10LA) was treated with 10mM lactic acid for 24 hours; 3. The lithium carbonate treatment group (LA) was treated with 1mM lithium carbonate for 24 hours; 4. The lactic acid/lithium carbonate group (10LALC) was treated with 10mM lactic acid and 1mM lithium carbonate for 24 hours.&amp;nbsp;</dc:description>
  <dc:subject>CD8+T; Lactylation; chip-seq; lithium carbonate</dc:subject>
  <dc:creator>唐亮</dc:creator>
  <dc:creator>黄波</dc:creator>
  <dc:creator>JING WEI MA</dc:creator>
  <dc:creator>YAO YAO TAN</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.1038/s41590-023-01738-0</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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