优化非洲猪瘟病毒检测 pcr 试验方法中的引物浓度和退火温度

L. D. Anggreni, Ni Made Ritha Krisna Dewi, I. G. N. K. Mahardika, I. G. N. N. Putra
{"title":"优化非洲猪瘟病毒检测 pcr 试验方法中的引物浓度和退火温度","authors":"L. D. Anggreni, Ni Made Ritha Krisna Dewi, I. G. N. K. Mahardika, I. G. N. N. Putra","doi":"10.24843/bvu.v16i1.88","DOIUrl":null,"url":null,"abstract":"African Swine Fever disease causes high fatality number in domestic pigs. The most sensitive and specific laboratory diagnotic is PCR. The successful of PCR is determined by DNA quality, Annealing temperature, MGCl2 concentration, polymerase enzymes, primer concentration, and PCR cycles. The Annealing process requires in the right temperature. The difference annealing temperature causes amplification process failure. The specificity and sensitivity of PCR products are determined by the optimal annealing temperature. PCR optimization, variations of time, temperature, and primer concentration can be adjusted. This study was conducted by PCR testing to detect DNA ASF virus using primer concentration and the most optimum Annealing temperature. Identification of primer concentrations and annealing temperature begins to make PCR components volume 10 µl consist of 5µL PCR Master Mix, a pair of ASF primer 0.5 µl, 1µL DNA templates, and 3µL ddH2O. The PCR component is processed in a thermocycler with a temperature condition of 95°C pre-denaturation for 5 minutes, and denaturation at 94°C for 45 seconds. The gradient annealing temperature starts at 50°C, 52°C, 55°C, 59°Cm and 65°C for 1 minute. Temperature 72 ° C for synthesis 1 minute. repetition of the cycle is 34 times. Final synthesis for 72°C for 5 minutes, the storage temperature is 22°C. The result of optimization at the primer concentration of 10 µm obtained a cleared band according to the target compared to the primary concentration of 5 µm. The best annealing temperature in this research is 55 °C. If the Annealing temperature is given lower, causing primer attachment to the DNA template is not specific so non-specific PCR products are formed many bands. Conversely, if the annealing temperature is higher, causing primary attachment to the template DNA will be released so that the band that appears is very thin PCR product is not formed does not appear.","PeriodicalId":30995,"journal":{"name":"Buletin Veteriner Udayana","volume":"231 20","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"OPTIMISATION OF PRIMER CONCENTRATION AND ANNEALING TEMPERATURE IN PCR TEST METHOD FOR AFRICAN SWINE FEVER VIRUS DETECTION\",\"authors\":\"L. D. Anggreni, Ni Made Ritha Krisna Dewi, I. G. N. K. Mahardika, I. G. N. N. Putra\",\"doi\":\"10.24843/bvu.v16i1.88\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"African Swine Fever disease causes high fatality number in domestic pigs. The most sensitive and specific laboratory diagnotic is PCR. The successful of PCR is determined by DNA quality, Annealing temperature, MGCl2 concentration, polymerase enzymes, primer concentration, and PCR cycles. The Annealing process requires in the right temperature. The difference annealing temperature causes amplification process failure. The specificity and sensitivity of PCR products are determined by the optimal annealing temperature. PCR optimization, variations of time, temperature, and primer concentration can be adjusted. This study was conducted by PCR testing to detect DNA ASF virus using primer concentration and the most optimum Annealing temperature. Identification of primer concentrations and annealing temperature begins to make PCR components volume 10 µl consist of 5µL PCR Master Mix, a pair of ASF primer 0.5 µl, 1µL DNA templates, and 3µL ddH2O. The PCR component is processed in a thermocycler with a temperature condition of 95°C pre-denaturation for 5 minutes, and denaturation at 94°C for 45 seconds. The gradient annealing temperature starts at 50°C, 52°C, 55°C, 59°Cm and 65°C for 1 minute. Temperature 72 ° C for synthesis 1 minute. repetition of the cycle is 34 times. Final synthesis for 72°C for 5 minutes, the storage temperature is 22°C. The result of optimization at the primer concentration of 10 µm obtained a cleared band according to the target compared to the primary concentration of 5 µm. The best annealing temperature in this research is 55 °C. If the Annealing temperature is given lower, causing primer attachment to the DNA template is not specific so non-specific PCR products are formed many bands. Conversely, if the annealing temperature is higher, causing primary attachment to the template DNA will be released so that the band that appears is very thin PCR product is not formed does not appear.\",\"PeriodicalId\":30995,\"journal\":{\"name\":\"Buletin Veteriner Udayana\",\"volume\":\"231 20\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Buletin Veteriner Udayana\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.24843/bvu.v16i1.88\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Buletin Veteriner Udayana","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24843/bvu.v16i1.88","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

非洲猪瘟会导致家猪高死亡率。最灵敏、最特异的实验室诊断方法是 PCR。PCR 成功与否取决于 DNA 质量、退火温度、MGCl2 浓度、聚合酶、引物浓度和 PCR 循环。退火过程需要合适的温度。退火温度不同会导致扩增过程失败。PCR 产物的特异性和灵敏度取决于最佳退火温度。PCR 优化、时间、温度和引物浓度的变化都可以进行调整。本研究利用引物浓度和最适退火温度进行了检测 DNA ASF 病毒的 PCR 测试。确定引物浓度和退火温度后,开始制作体积为 10 µl 的 PCR 组件,其中包括 5µL PCR Master Mix、一对 ASF 引物 0.5 µl、1µL DNA 模板和 3µL ddH2O。PCR 成分在热循环仪中处理,温度条件为 95°C 预变性 5 分钟,94°C 变性 45 秒。梯度退火温度从 50°C、52°C、55°C、59°Cm 和 65°C 开始,持续 1 分钟。温度 72°C 合成 1 分钟。循环重复 34 次。最终合成温度为 72°C 5 分钟,保存温度为 22°C。优化结果显示,与 5 µm 的引物浓度相比,10 µm 的引物浓度下获得的目标条带清晰。本研究的最佳退火温度为 55°C。如果退火温度较低,会导致引物与 DNA 模板的附着不特异,从而形成许多条带的非特异性 PCR 产物。反之,如果退火温度较高,则会释放附着在模板 DNA 上的引物,这样出现的条带就会很薄,PCR 产物就不会出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
OPTIMISATION OF PRIMER CONCENTRATION AND ANNEALING TEMPERATURE IN PCR TEST METHOD FOR AFRICAN SWINE FEVER VIRUS DETECTION
African Swine Fever disease causes high fatality number in domestic pigs. The most sensitive and specific laboratory diagnotic is PCR. The successful of PCR is determined by DNA quality, Annealing temperature, MGCl2 concentration, polymerase enzymes, primer concentration, and PCR cycles. The Annealing process requires in the right temperature. The difference annealing temperature causes amplification process failure. The specificity and sensitivity of PCR products are determined by the optimal annealing temperature. PCR optimization, variations of time, temperature, and primer concentration can be adjusted. This study was conducted by PCR testing to detect DNA ASF virus using primer concentration and the most optimum Annealing temperature. Identification of primer concentrations and annealing temperature begins to make PCR components volume 10 µl consist of 5µL PCR Master Mix, a pair of ASF primer 0.5 µl, 1µL DNA templates, and 3µL ddH2O. The PCR component is processed in a thermocycler with a temperature condition of 95°C pre-denaturation for 5 minutes, and denaturation at 94°C for 45 seconds. The gradient annealing temperature starts at 50°C, 52°C, 55°C, 59°Cm and 65°C for 1 minute. Temperature 72 ° C for synthesis 1 minute. repetition of the cycle is 34 times. Final synthesis for 72°C for 5 minutes, the storage temperature is 22°C. The result of optimization at the primer concentration of 10 µm obtained a cleared band according to the target compared to the primary concentration of 5 µm. The best annealing temperature in this research is 55 °C. If the Annealing temperature is given lower, causing primer attachment to the DNA template is not specific so non-specific PCR products are formed many bands. Conversely, if the annealing temperature is higher, causing primary attachment to the template DNA will be released so that the band that appears is very thin PCR product is not formed does not appear.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
83
审稿时长
8 weeks
期刊最新文献
LEVEL OF KNOWLEDGE AND IMPLEMENTATION OF CATTLE BARN BIOSECURITY RELATED TO PREVENTION OF FOOT AND MOUTH DISEASE IN GIANYAR BALI PREVALENCE OF GASTROINTESTINAL NEMATODES INFECTION IN BALI CATTLE CALVES AT BERINGKIT ANIMAL MARKET BADUNG REGENCY YEAST POPULATION OF SACCHAROMYCES CEREVISIAE IN THE FECES OF YOUNG AND ADULT ETAWA CROSSBREED GOATS IN SUKAWATI DISTRICT, GIANYAR REGENCY GROWTH RATE OF BODY LENGTH AND HEIGHT OF MALE BALI CATTLE DURING FATTENING VARIATIONS OF COLIFORM BACTERIA ISOLATED FROM BALI CATTLE CALVES FECES, MARKETED AT BERINGKIT ANIMAL MARKET
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1