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6篇 您的检索式:作者名="Devananda"
    题名 作者 年代 出处 被引量
1Particle size of granules and mechanical properties of paracetamol tablets 显示文摘Biresh K S Devananda J Rameh P 2011Int J Pharm Sei Rev Res2011,8,2:1
2gcpA ( stm1987 ) is critical for cellulose production and biofilm formation on polystyrene surface by Salmonella enterica serovar Weltevreden in both high and low nutrient medium显示文摘Patit Paban Bhowmick Devananda Devegowda H.A. Darshanee Ruwandeepika Thilo M. Fuchs Shabarinath Srikumar Iddya Karunasagar Indrani Karunasagar 2010Microbial Pathogenesis2010,,2:1
3Ef- fect of machining parameters and heat treatment on the residual stress distribution in titanium alloy IMI-834 显示文摘Sridhar B R Devananda G Ramachandra K 2003Journal of Materials Processing Technology2003,139,:1
4Effect of machining parameters and heat treatment on the residual stress distribution in titanium alloy IMI-834显示文摘SRIDHAR B R DEVANANDA G 2003Journal of material processing technology2003,139,:1
5Effect ofmachining parameters and heat treatment on the residual stressdistribution in titanium alloy IMI-834显示文摘Sridhar B R Devananda G Ramachandra K 2003Journal of MaterialsProcessing Technology2003,139,13:1
6DNA extraction from archived hematoxylin and eosin-stained tissue slides for downstream molecular analysis显示文摘BACKGROUND Histopathologically stained archived tissue slides are stored in hospital archives for years to decades.They are the largest available source of biological materials and are a potentially useful resource that can be used for retrospective epidemiological studies.DNA recovered from the slides can be used for several downstream molecular processes including polymerase chain reaction,single nucleotide polymorphism analysis,and whole genome sequencing.The DNA from these slides can be utilized to compare gene signatures of normal and diseased tissues.However,extraction of high-quality DNA from archived stained hematoxylin and eosin(H&E)slides remains challenging.AIM To standardize a new protocol for extracting DNA from archived H&E-stained tissue slides for further molecular assays.METHODS A total of 100 archived H&E-stained cancer slides were subjected to a total of five methods of DNA extraction.Methods were varied in the deparaffinization step,tissue rehydration,duration of lysis,and presence or absence of proteinase K.The extracted DNA was quantified using a NanoDrop spectrophometer and the quality was analyzed by agarose gel electrophoresis.Then each sample was subjected to polymerase chain reaction(PCR)to amplify the internal control gene GAPDH,thereby confirming the DNA intactness,which could be further utilized for other downstream applications.RESULTS Of the five different methods tested,the third method wherein xylene was used for tissue deparaffinization followed by 72 h of digestion and without proteinase K inactivation yielded the highest amount of DNA with good purity.The yield was significantly higher when compared to other methods.In addition,90%of the extracted DNA showed amplifiable GAPDH gene.CONCLUSION Here we present a step-by-step,cost-effective,and reproducible protocol for the extraction of PCR-friendly DNA from archived H&E-stained cancer tissue slides that can be used for further downstream molecular applications.Pushkal Sinduvadi Ramesh Venkatesh Madegowda Suprith Kumar Shailashree Narasimha Parichay S R Nandini Nandish Manoli Devananda Devegowda 2019World Journal of Methodology2019,9,3:0
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