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Isolation of DNA for RAPD Analysis From Dry Leaf Material of Some Hesperis L. Specimens

机译:从一些绣球花干叶材料中提取用于RAPD分析的DNA

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摘要

An improved protocol for the isolation of DNA from dry material of some Hesperis specimens is described. The isolated DNA is suitable for random amplification of polymorphic DNA (RAPD) analysis. Different DNA extraction protocols were examined to determine which might yield DNA from dry leaf tissue of Hesperis specimens. The methods examined include the protocols with hexadecyltrimethylammonium bromide (CTAB) described by Doyle and Doyle (1987); sodium dodecyl sulfate (SDS) by Della-porta et al. (1983); and CTAB and SDS, the modified minipreparation, by Dellaporta et al (1983). None of these procedures yielded DNA of suitable purity for RAPD assay. We established an improved procedure involving CTAB and enzymatic digestion of proteins and RNA. The recovery of DNA with an average yield of 25 mg/g of leaf material was possible with this procedure. RAPD bands, which could be used to distinguish among Hesperis specimens, were generated.
机译:描述了一种从某些Hesperis标本的干燥材料中分离DNA的改进方案。分离的DNA适用于多态性DNA(RAPD)分析的随机扩增。检查了不同的DNA提取方案,以确定哪些可能从Hesperis标本的干叶组织中产生DNA。所研究的方法包括Doyle和Doyle(1987)描述的使用十六烷基三甲基溴化铵(CTAB)的方案。 Della-porta等人的十二烷基硫酸钠(SDS)。 (1983); Dellaporta等人(1983)的改良微型制剂CTAB和SDS。这些程序均未产生用于RAPD分析的合适纯度的DNA。我们建立了涉及CTAB以及蛋白质和RNA酶消化的改进程序。用这种方法可以回收平均叶料量为25 mg / g的DNA。生成了可用于区分Hesperis标本的RAPD带。

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