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ISSN 1001-5256
CN 22-1108/R
Issue 1
Jan.  2001
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大鼠肝再生增强因子基因组DNA的克隆化与序列分析

  • Published Date: 2001-01-20
  • WT5”BZ]To investigate the structure of the genomic DNA sequence for ALR, specific PCR method was used to sub clone target fragment from the Wistar rat genome The whole length is 1508bp, including 3 exons and 2 introns The exons are 18bp, 197bp and 163bp, each one encode 6aa, 64aa and 55aa respectively The lengths of the exon are as long as that of human and mouse [WT5”HZ]

     

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  • [1]HagiyaM , FrancavillaA , PolimegeL , etal Cloningandsequenceanalysisoftheaugmenterofliverregeneration (ALR) gene:expres sionofbiologicallyactiverecombinantALRanddemonstrationoftis suedistribution[J] PNASUSA , 1994, 91∶814 2
    [][2 ]成军 , 陈菊梅 肝再生增强因子研究进展 [J] 肝脏 , 1999, 4∶117
    [][3 ]成军 , 钟彦伟 , 刘妍 , 等 人肝再生增强因子基因组DNA的克隆化与序列分析 [J] 中华肝脏病杂志 , 2 0 0 0 , 8∶12
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      沈阳化工大学材料科学与工程学院 沈阳 110142

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