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上样量和洗脱液温度影响磁珠法纯化mRNA效果 被引量:1

Influence of Loading Amount and Eluant Temperature to Effect of mRNA Purification by Magnetic Particles
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摘要 对总RNA上样量和洗脱液温度的比较试验表明,用Promega公司生产的磁珠法试剂盒PolyAT-tractmRNAIsolationSystemsⅢZ5300纯化mRNA,每管总RNA上样量以550滋g适中。将洗脱液加热至R70℃,有利于提高洗脱率。550滋g上样量与70℃洗脱液温度配合运用,既可保证mRNA纯化质量,充分利用总RNA样品,又可避免磁珠浪费。 Comparative experiment among different loading amount and eluant temperature showed that the optimal loading amount for magneticsphere mRNA purification kit produced by Promega (PolyA TtractR mRNA Isolation Systems Ⅲ Z5300) was about 550μg. Heating the eluant to 70℃ was beneficial to raising elution ratio. Using loading amount of 550 μg together with eluant temperature of 70℃ not only ensures the quality of mRNA purification and utilizes total RNA sample, but also avoids the waste of magnetic particles.
作者 倪娜 李晚忱
出处 《分子植物育种》 CAS CSCD 2005年第2期282-284,共3页 Molecular Plant Breeding
关键词 磁珠法 洗脱液 总RNA 纯化 效果 配合 试剂盒 比较试验 温度 利用 Loading amount,Eluant temperature,Magnetic particle,mRNA purification
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  • 1Albretsen C., Kalland K.H., Haukanes B.I., Havarstein L.S., and Kleppe K., 1990, Applications of magnetic beads with covalently attached oligonucleotides in hybridization: isolation and detection of specific measles virus mRNA from a crude cell lysate, Anal. Biochem., 189(1): 40-50
  • 2Edmonds M., Vaughan M.H., and Nakazato H., 1971, Polyadenylic acid sequences in the heterogeneous nuclear RNA and rapidly-labeled polyribosomal RNA of hela cells: possible evidence for a precursor relationship, Proc. Natl. Acad. Sci., 68(6): 1336-1340
  • 3Hornes E., and Korsnes L., 1990, Magnetic DNA hybridization properties of oligonucleotide probes attached to superpara-magnetic beads and their use in the isolation of poly (A) mRNA from eukaryotic cells, Genet. Anal. Tech. Appl.,7(6): 145-150
  • 4Jakobsen K.S., Breivold E., and Hornes E., 1990, Purification of mRNA directly from crude plant tissues in 15 minutes using magnetic oligo dT microspheres, Nucleic Acids Res.,18(12): 3669

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  • 2Li X,Fan X,Zhang K,et al.Influence of psoriatic peripheral bloodCD4+T and CD8+T lymphocytes on C-myc,Bcl-xL and Ki67 geneexpression in keratinocytes[J].Eur J Dermatol,2007,17:392-396.
  • 3Wang Z,Gerstein M,Snyder M.RNA-Seq:a revolutionary tool fortranscriptomics[J].Nat Rev Genet,2009,10:57-63.
  • 4IrizarryRA,WarrenD,SpencerF,etal.Multiple-laboratorycomparisonof microarray platforms[J].Nat Methods,2005,2:345-350.
  • 5Pedotti P T,’t Hoen PA,Vreugdenhil E,et al.Can subtle changes ingene expression be consistently detected with different microarrayplatforms?[J].BMC Genomics,2008,9:124.
  • 6Pietrzak A,Lecewicz-Torun B,Chodorowska G,et al.Interleukin-18levels in the plasma of psoriatic patients correlate with the extent ofskin lesions and the PASI score[J].Acta Derm Venereol,2003,83:262-265.
  • 7Companjen A,van der Wel L,van der Fits L,et al.Elevatedinterleukin-18 protein expression in early active and proressiveplaque-typepsoriaticlesions[J].Eur CytokineNetw,2004,15:210-216.
  • 8T akahashi H,Manabe A,Ishida-Yamamoto A,et al.Aberrantexpression of apoptosis-related molecules in psoriatic epidermis[J].JDermatol Sci,2002,28:187-197.
  • 9Polyak K,KatoJY,Solomon MJ,et al.p27Kip1,a cyclin-cd inhibitor,links transforming growth factor-beta and contact inhibition to cellcycle arrest[J].Genes Dev,1994,8:9-22.
  • 10MasciulloV,SgambatoA,PacilioC,et al.Frequent loss of expressionof the cyclin-dependent kinase inhibitor p27 in epithelial ovariancancer[J].Cancer Res,1999,59:3790-3794.

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