共查询到19条相似文献,搜索用时 93 毫秒
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水稻基因组DNA微量提取 总被引:2,自引:0,他引:2
随着植物学向分子水平的深入发展,研究中经常需要获得高质量的植物DNA样品,因此,建立植物DNA提取与纯化的常规实验方法对教学和科研都显得非常必要。介绍一种快速提取微量DNA的方法,该方法简单易行,无需任何特殊设备,所需样品量少,提取的DNA纯度高,可满足以PCR扩增为基础的实验需要。 相似文献
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玉米基因组DNA提取及浓度测定方法评价 总被引:2,自引:0,他引:2
以非转基因玉米种子为材料,比较了常用的3种植物基因组DNA提取试剂盒及改良的CTAB法,通过琼脂糖凝胶电泳、紫外分光光度及实时荧光PCR扩增检测,对提取得到的基因组DNA的纯度、得率及4种提取方法的重复性、提取时间进行分析;比较紫外分光光度法、Qubit荧光法、Pico Green荧光分光光度法,以实时荧光定量PCR检测结果为参照,对3种DNA浓度测定方法的准确性进行分析.结果显示,磁珠法(Promega)最适合应用于快速、简便、高效检测中的植物基因组DNA提取,能有效获得纯度高、完整性好的基因组DNA,并且磁珠法提取效率高,重复性好,提取时间短;在基因组DNA浓度测定中,紫外分光光度法、Qubit荧光法、Pico Green荧光分光光度法的相对误差分别为99.8%、49.8%和28.9%,表明Pico Green荧光分光光度法测定DNA浓度的准确度最高. 相似文献
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一种蜘蛛基因组DNA的简易提取方法 总被引:6,自引:0,他引:6
本文介绍了1种改进的蜘蛛基因组DNA的提取方法.通过与传统DNA提取方法的比较,本方法具有可在常温条件下进行、DNA得率高、简便、经济等优势. 相似文献
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Michiels A Van den Ende W Tucker M Van Riet L Van Laere A 《Analytical biochemistry》2003,315(1):85-89
The isolation of intact, high-molecular-mass genomic DNA is essential for many molecular biology applications including long PCR, endonuclease restriction digestion, Southern blot analysis, and genomic library construction. Many protocols are available for the extraction of DNA from plant material. However, for latex-containing Asteraceae (Cichorioideae) species, standard protocols and commercially available kits do not produce efficient yields of high-quality amplifiable DNA. A cetyltrimethylammonium bromide protocol has been optimized for isolation of genomic DNA from latex-containing plants. Key steps in the modified protocol are the use of etiolated leaf tissue for extraction and an overnight 25 degrees C isopropanol precipitation step. The purified DNA has excellent spectral qualities, is efficiently digested by restriction endonucleases, and is suitable for long-fragment PCR amplification. 相似文献
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Suzuki Setsuko Kensuke Yoshimura Saneyoshi Ueno James Raymond Peter Worth Tokuko Ujino-Ihara Toshio Katsuki Shuichi Noshiro Tomoyuki Fujii Takahisa Arai Hiroshi Yoshimaru 《Molecular ecology resources》2023,23(4):855-871
DNA barcode databases are increasingly available for a range of organisms, facilitating the wide application of DNA barcode-based studies. Here we announce the development of a comprehensive DNA barcode reference library of Japanese native woody seed plants representing 43 orders, 99 families, 303 genera and 834 species, and comprising 77.3% of the genera and 72.2% of the species of native woody seed plants in Japan. A total of 6216 plant specimens were collected from 223 sites across the subtropical, temperate, boreal and alpine biomes in Japan with most species represented by multiple accessions. This reference library utilized three chloroplast DNA regions (rbcL, trnH-psbA and matK) and consists of 14,403 barcode sequences. Individual regions varied in their identification rates, with species-level and genus-level rates for rbcL, trnH-psbA and matK based on blast being 57.4%/96.2%, 78.5%/99.1% and 67.8%/98.1%, respectively. Identification rates were higher using region combinations, with total species-level rates for two region combinations (rbcL & trnH-psbA, rbcL & matK and trnH-psbA & matK) ranging between 90.6% and 95.8%, and for all three regions being equal to 98.6%. Genus-level identification rates were even higher, ranging between 99.7% and 100% for two region combinations and being 100% for the three regions. These results indicate that this DNA barcode reference library is an effective resource for investigations of native woody seed plants in Japan using DNA barcodes and provides a useful template for the development of libraries for other components of the Japanese flora. 相似文献
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荔枝基因组DNA的提取 总被引:12,自引:0,他引:12
介绍一种提取荔枝基因组DNA的有效方法,即在传统CTAB法的基础上,于CTAB抽提液中加入1%的PVP。影响荔枝基因组DNA提取质量的因素有3个:第一是取材,第二是磨样与温育时间,第三是防止褐化。 相似文献
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蜜源木本植物的鉴定能为中华蜜蜂Apis cerana cerana保护和利用提供依据.本研究从在秦岭地区收集的4份中华蜜蜂蜂蜜中分离出植物花粉,然后在扫描电镜下观察花粉形态,根据花粉大小、赤道面观、极面观、表面纹饰对花粉所属植物的种类进行鉴定.共鉴定出中华蜜蜂利用的蜜源木本植物13科,19属,20种.其中以壳斗科Fagaceae、忍冬科Caprifoliaceae最多,卫矛科Celastraceae、桦木科Betulaceae、蔷薇科Rosaceae次之.这些蜜源木本植物中有13种是药用植物.秦岭地区丰富的蜜源木本植物为中华蜜蜂的生存提供了食物资源;同时中华蜜蜂作为传粉昆虫,对维持秦岭地区蜜源植物的生存和生态系统稳定起着重要的作用. 相似文献
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松突圆蚧基因组DNA提取方法的比较 总被引:1,自引:0,他引:1
分别采用醋酸钾(KAc)法、十二烷基硫酸钠-蛋白酶K(SDS-PK)消化法、十六烷基三乙基溴化铵(CTAB)法及DNA提取试剂盒(吸附柱型)对单只松突圆蚧的基因组DNA进行提取。同时针对盾蚧科昆虫的特点,在提取前利用氯仿和解剖针去除样品表面的介壳。结果表明,用同种提取方法提取的经氯仿处理与未经处理样本的提取效果无明显差异,而采用解剖针去除介壳的样本提取效果较好。所采用的4种提取方法均能从新鲜标本中提取出DNA,其中CTAB法提取的DNA量较多,而SDS-PK法提取的DNA质量较好。 相似文献
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药用木本植物的生态保护 总被引:5,自引:1,他引:5
在分析我国药用木本植物的利用现状和特殊性的基础上。揭示了药用木本植物保护与利用之间的矛盾。提出了解决矛盾的根本出路和需要开展的基础研究工作.研究成树主要药用成分的器官分布、季节变化、年龄差异以及与环境因素的相关性;研究幼树主要药用成分的器官分布、季节变化特别是年龄差异;研究环境因素(培育条件)对幼树主要药用成分的影响和调控规律;进一步从蛋白质(主要药用成分代谢过程中的关键酶)和核酸(关键酶的编码基因)水平解析环境因子对幼树主要药用成分的调控机理. 相似文献