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产品目录
  • 细胞培养进口血清
    进口胎牛血清
    进口新生牛血清
    进口猪血清
    马血清
  • 支原体检测盒及标准品
    常规PCR检测试剂盒
    荧光定量PCR检测(qPCR法)
    支原体DNA提取
    灵敏度标准品(方法验证用)
    特异性标准品(方法验证用)
    PCR定量标准品(可用于方法验证)
  • 支原体祛除试剂
    细胞中支原体祛除
    环境支原体祛除
    水槽支原体祛除
  • 干细胞培养基
  • DNA/RNA污染祛除
    DNA/RNA污染祛除试剂
    DNA污染监测
  • RNA病毒研究试剂
    RNA病毒检测试剂盒
    病毒RNA提取
  • PCR仪器及配套产品
    DNA污染监测祛除
    PCR/qPCR仪性能检查
    PCR试剂
    PCR试剂盒
    PCR预混液(冻干粉)
    热启动聚合酶MB Taq DNA
  • 微生物PCR检测
    食品检测类产品
    食品微生物检测
    细菌PCR检测

【系列2】胎牛血清RNA干扰了细胞培养外源性RNA

2016-10-11 14:20

FBS-derived miR-1246 is detected in cultured mouse cells

The additional question of broader importance is whether FBS-associated RNA may interfere with cellular RNA analysis. MiR-1246 gene that encodes one of the most abundantly expressed miRNAs in FBS, is present in only 4 out of 223 species, including bovine, human, orangutan and chimpanzee, but not in mouse or rat17. There are no sequences homologous to hsa-miR-1246 identified in the mouse genome. However, low levels of mature miR-1246 were consistently and reproducibly detected in all tested mouse cell lines cultured with 10% FBS (Fig. 1h) by both LNA-based SYBR Green assay (Exiqon) and TaqMan assay (Thermo Fisher Scientific). miR-1246 signal varied between the recipient cells lines, suggesting different levels of uptake and/or processing in the different cells. The miR-1246 signal was significantly reduced in cells that were switched to 10% vdFBS culture medium seven days prior to RNA isolation and undetectable in mouse tissues (Fig. 1h). This example suggests that FBS RNA complexes associated with EVs and possibly non-vesicular RNPs as well, might be taken up by cultured cells and interfere with the quantification of cellular RNA. Considering highly sensitive expression profiling technologies commonly utilized in current research that are capable of detecting femtomoles of RNA, further in-depth analysis of FBS RNA-associated confounders is warranted. As of today, there are no data suggesting the functional activity of this low-level bovine RNA in the recipient cells; nevertheless, subsequent work will be required to accurately address its impact.

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