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DNA电泳带型分析
DNA电泳需要进行带型分析,在实验过程中常会发现所得的带型出现在这样那样的问题。在此,对DNA带型做了相应的分析。带型原因分析解决办法弱带或无带上样的DNA量不
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琼脂糖凝胶电泳迁移速率的影响因素
1、DNA的分子大小及构型不同构型DNA的移动速度次序为:供价闭环DNA(covalently closed circular,cccDNA)>直线DNA
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凝胶迁移或电泳迁移率实验(EMSA)
凝胶迁移或电泳迁移率实验(EMSA)是一种研究DNA结合蛋白和其相关的DNA结合序列相互作用的技术,可用于定性和定量分析。这一技术最初用于研究DNA结合蛋白,目
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Sending Sera to Testing for Mouse Pathogens.
Sending Sera to Testing for Mouse Pathogens.Bleed mice: Obtain 300-400µl from mi
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Karyotyping Xenopus embryos
This protocol was provided to us from the Grainger lab and modified by M. Khokha
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ES injection pipette manufacture
ES injection pipette manufactureThe following is an outline of the method that I
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DIFFERENTIAL DISPLAY
Comparible RNAs were isolated from different treatments using my favorite method
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Differential Display Technical notes
Optimal arbitrary primer length for Differential Display The concept of differen
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Superovulation of Mice
Given each mouse 0.05 ml PMSG (Straight from vial), administered i/p at 12 o'
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Transgenic Animals
Transgenic AnimalsThe term “transgenic animals” describes animals whose chromoso
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DNA Preparation for Microinjection or Electroporation
This protocol was developed by Jan Parker-Thornburg at The Ohio State Universtiy
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Molecular Analysis and Results - DNA
Theory of CGH Comparative genomic hybridization (CGH) is a fairly new molecular
2024-09-25 22 -
Microinjection of dsRNA into Mouse Oocytes and Early Embryos
Microinjection of dsRNA into Mouse Oocytes and Early EmbryosPaula Stein and Petr
2024-09-25 24 -
PROTOCOLES MICROSATELLITES / MICROSATELLITE PROTOCOLS
Microsatellite markers: isolation with non-radioactive probes and amplification
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Mutation Detection By Single-Strand Conformational Polymorphism (SSCP)
PCR Protocol10X PCR Buffer1.0MgCl2 (2.0mM)0.8µldNTPS mix*0.8µlPrimer-F (µg/µl)0.
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