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    <identifier>10.57760/sciencedb.23715</identifier>
    <datestamp>2025-04-23T09:04:40Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-04-23</dc:date>
  <dc:title>Mitochondrial transcription factor A (TFAM) was knocked down in HTR-8/SVneo cells</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.23715</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>As shown in the supplementary Figure 1 A,&amp;nbsp;HTR-8/SVneo cells were transfected with negative control siRNA and three different sequences of siTFAM, respectively. Compared with the blank control group, TFAM mRNA levels in the negative control group showed no statistical difference (P = 0.467), but were significantly decreased in siTFAM #1, #2 and #3 (P &amp;lt; 0.001). Furthermore, TFAM protein expression decreased after transfection of siTFAM #1 (B). Moreover, ND-1/&amp;beta;2M and COX-3/&amp;beta;2M in the siTFAM group were significantly lower than those in the negative control group (P = 0.001; P &amp;lt; 0.001), indicating that the mtDNA copy number of trophoblast cells was significantly decreased (C, D).&amp;nbsp;*P&amp;lt; 0.05; **P&amp;lt; 0.01; ***P&amp;lt; 0.001.</dc:description>
  <dc:subject>TFAM; supplementary; HTR-8/SVneo cells</dc:subject>
  <dc:creator>Hui-Ying Jie</dc:creator>
  <dc:creator>Lu Luo</dc:creator>
  <dc:creator>Bing Cai</dc:creator>
  <dc:creator>Yan Xu</dc:creator>
  <dc:creator>Yuan Yuan</dc:creator>
  <dc:creator>Yang-Xing Wen</dc:creator>
  <dc:creator>Si-Min Liu</dc:creator>
  <dc:creator>Ji-Fan Tan</dc:creator>
  <dc:creator>Ming-Hui Chen</dc:creator>
  <dc:creator>Can-Quan Zhou</dc:creator>
  <dc:creator>Qing-Yun Mai</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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