MiRNA remain stable for detection and PCR-based amplification in FFPE tissue samples. Several miRNA extraction kits are available, however miRNA fraction, as part of total RNA '/> miRNA Isolation from FFPET Specimen: A Technical Comparison of miRNA and Total RNA Isolation Methods
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miRNA Isolation from FFPET Specimen: A Technical Comparison of miRNA and Total RNA Isolation Methods

机译:FFPET标本中的miRNA分离:miRNA和总RNA分离方法的技术比较

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id="Par1" class="Para">MiRNA remain stable for detection and PCR-based amplification in FFPE tissue samples. Several miRNA extraction kits are available, however miRNA fraction, as part of total RNA can be isolated using total RNA purification methods, as well. Our primary aim was to compare four different miRNA and total RNA isolation methods from FFPE tissues. Further purposes were to evaluate quantitatively and qualitatively the yield of the isolated miRNA. MiRNAs were isolated from normal colorectal cancer FFPE specimens from the same patients. Two miRNA isolation kits (High Pure miRNA Isolation Kit, miRCURYa?¢ RNA Isolation Kit) and two total RNA isolation kits were compared (High Pure RNA Paraffin Kit, MagNA Pure 96 Cellular RNA LV Kit). Quantity and quality were determined, expression analysis was performed by real-time PCR using qPCR Human Panel I??+??II (Exiqon) method detecting 742 human miRNAs in parallel. The yield of total RNA was found to be higher than miRNA purification protocols (in CRC: Ex: 0203???±??0021????g; HPm: 1,45???±??0,8????g; HPp: 21,36???±??4,98????g; MP: 8,6???±??5,1????g). MiRNAs were detected in lower relative quantity of total RNA compared to the miRNA kits. Higher number of miRNAs could be detected by the miRNA isolation kits in comparison to the total RNA isolation methods. (Ex: 497???±??16; HPm: 542???±??11; HPp: 332???±??36; MP: 295???±??74). Colon specific miRNAs (miR-21-5p;-34-5p) give satisfying results by miRNA isolation kits. Although miRNA can be detected also after total RNA isolation methods, for reliable and reproducible miRNA expression profiling the use of miRNA isolation kits are more suitable.
机译:id =“ Par1” class =“ Para”> MiRNA对于FFPE组织样品中的检测和基于PCR的扩增保持稳定。可以使用几种miRNA提取试剂盒,但是也可以使用总RNA纯化方法分离出总RNA中的miRNA部分。我们的主要目的是比较FFPE组织中的四种不同的miRNA和总RNA分离方法。进一步的目的是定量和定性评估分离的miRNA的产量。从相同患者的正常结直肠癌FFPE标本中分离出miRNA。比较了两种miRNA分离试剂盒(高纯度miRNA分离试剂盒,miRCURYaTM RNA分离试剂盒)和两种总RNA分离试剂盒(高纯RNA石蜡试剂盒,MagNA Pure 96细胞RNA LV试剂盒)。确定数量和质量,使用qPCR Human Panel I + + II(Exiqon)方法通过实时PCR进行表达分析,并行检测742个人miRNA。发现总RNA的产量高于miRNA纯化方案(在CRC中:Ex:0203±±0021μg; HPm:1.45±0.8μg。 ; g; HPp:21,36±4,98±g; MP:8,6±5,1,5±g。与miRNA试剂盒相比,检测到的miRNA的总RNA相对含量较低。与总RNA分离方法相比,通过miRNA分离试剂盒可以检测到更多数量的miRNA。 (例如:497 ???±16; HPm:542 ???±11; HPp:332 ???±36; MP:295 ???±74)。结肠特异的miRNA(miR-21-5p; -34-5p)通过miRNA分离试剂盒获得令人满意的结果。尽管在总RNA分离方法后也可以检测到miRNA,但对于可靠且可重现的miRNA表达谱,使用miRNA分离试剂盒更为合适。

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