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Polymerase Chain Reaction (PCR) to Amplify rRNA Gene Fragment
Polymerase Chain Reaction (PCR) to Amplify rRNA Gene Fragment Prepare sufficient
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PCR基本实验方法(二)
Recommended Reaction Conditions: Initial Conditions:Initial denaturation at star
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PCR clean up using 3M sodium acetate and chilled absolute ethanol
For each 20 ul of PCR product, prepare the following mixture in 1.5 ml Tube.2 ul
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Degenerate PCR Detailed guide
Degenerate PCR by Michael Koelle The identification of novel members of gene fam
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Differential Display of Cotton Transcripts
Plant MaterialsCotton ovules (Gossypium hirsutum cv. Coker 312) were collected 8
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PCR的下游应用
・ Agarose Gel Electrophoresis of PCR Products (Robert H. Cruickshank)・
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PCR Technology
Introduction Polymerase chain reaction (PCR) has rapidly become one of the most
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Troubleshooting for PCR and multiplex PCR
Troubleshooting for PCR and multiplex PCRTroubleshooting discussion is based on
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PCR Primers For Gene Expression Detection or Quantification
Why PrimerBank?PrimerBank is a public resource for PCR primers. These primers ar
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CGH of PCR Amplified Microdissected DNA
PCR:We generally use 1-2 ul of starting paraffin microdissected DNA for each 50
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Primer Design Rules for Bisulfite Conversion Based PCR
Primer Design Rules for Bisulfite Conversion Based PCRAuthor: Long-Cheng LiSourc
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PCR and multiplex PCR guide
PCR and multiplex PCR guide Table below lists the parameters influencing the PCR
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RAPD技术应用中的一些问题及对策
焦锋,楼程富 (浙江大学蚕学系,杭州 310029) 摘要:综述了RAPD技术的一些理论性问题,包括RAPD与其它分子标记技术相比的优点,影响结果重复性的因素,
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Site-directed Mutagenesis using PCR
Site-directed Mutagenesis using PCR Michael P. Weiner, Tim Gackstetter, Gina L.
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AluPCR:用重复序列引物扩增来源复杂的人DNA
引言 聚合酶链反应PCR使不同来源的特异核酸片段的分离及分析发生了革命,但应用PCR分 离,分析特定DNA区域需要了解靶区域的边侧序列,这使扩增局限于已知DN
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