生物医学方面有关论文范文资料,与现代生物医学进展相关论文目录怎么自动生成
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培养基+1%PS的培养液.在液氮罐中取出HepG2冻存管,迅速放入37℃水浴箱中复温解冻,在超净台中吸取10ml培养液加入离心管中,待HepG2解冻后,用吸管吸出解冻液,加入离心管中,吹打混匀,密封后置离心机中离心(800r/min,5min),弃上清,加入配制好的培养液适当稀释,移入培养瓶中,于37℃5%CO2培养箱中常规培养.隔天换液,当HepG2生长融合成单层时,用PBS洗涤三遍,再用0.25%胰酶-0.02%EDTA消化传代.1.分组传代好的HepG2分组浓度为0mmol/L对照组1.0mmol/L,2.0mmol/L,4.0mmol/L,8.0mmol/L(乳酸1.0mmol/L+DCA,2.0mmol/L+DCA,4.0mmol/L+DCA,8.0mmol/L+DCA(DCA组),DCA终浓度为10-3mmol/L培养液共同培养24.
1.2.3四氮唑蓝(MTT)比色实验将HePG2细胞悬液浓度调整为5×l07/L,每孔200μL接种于96孔板上,各组分别加入不同浓度的乳酸,对照组不加药,另设空白对照孔只加培养基,无细胞,每组设8个重复孔.继续培养24后,加人MTT5g/L)20μL,放置孵箱内培养4h后弃上清,加人二甲基亚矾DMSO)200μL,振荡15min,用全自动酶标仪BIO-RAD550)检测490nm参考波长630nm处的吸光度值A值.抑制率%)等于(A对照-A实验/A对照×100%.
1.2.4流式细胞仪测定凋亡取各组细胞,分别用0.25%胰酶-0.02%EDTA消化30s,PBS洗涤后加入配制好的培养液制备成单细胞悬液,用细胞计数器调整每组细胞数为5×106/ml,取1ml细胞悬液于离心管中,置于离心机中800r/min离心5min,弃上清,PBS洗涤后轻轻振荡使细胞悬浮,反复离心洗涤后,取250μL细胞悬液,加入AnnexinV-FITC10μL和PI5μL,混匀后室温下避光孵育15min后上机待检.
1.统计学分析
研究型论文必须有统计学分析,注明所采用的统计学软件及版本号,检验方法及检验水准等.
2结果
应详细说明研究得到的真实数据或观察到的实验现象,并辅以图或表补充说明.
例:
2.1各组大鼠心肌细胞凋亡情况的比较
模型组大鼠AMI出现大量区心肌细胞凋亡凋亡细胞数显着多于假手术组P<,0.001),而OMT预处理使凋亡数显着减少P<,0.001),在组与OMT预处理假手术组中仅发现极少量的凋亡细胞存在.图
图1各组大鼠心肌细胞凋亡情况的比较
Fig.1Comparisonoftheapoptosisofratmyocardialcellsamongdifferentgroups
Note:Datawereexpressedas±SD,n等于6.***P<,0.001,paredwithgroupSham,###P<,0.001,paredwithAMIgroup.
例:
2.2胃癌细胞SGC7901的凋亡情况
流式细胞仪检测肿瘤细胞凋亡结果显示治疗组,阴性对照组及对照组胃癌细胞凋亡率分别为(22.28±0.12)%,(1.23±0.17)%和(1.03±0.14)%.治疗组与阴性对照组和对照组比较差异都有统计学意义t等于18.152,17.555,P<,0.05.见表1.
表1三组胃癌SGC7901细胞凋亡情况(%,x±s)
Table1ApoptosisastriccancerSGC7901ofthethreegroups
GroupsAmount(n)ApoptosisRateTreatmentGroup822.28±0.12#*NegativeControlGroup81.23±0.17ControlGroups81.03±0.14Note:paredwiththenegativegroup,#t等于18.152,paredwiththecontrolgroup,*t等于17.555,P<,0.05.
3讨论
对研究结果进行具体的总结应准确,简明,完整的分析各指标的意义,评价结果存在的误差,结合相关文献进行比较,说明结果产生的可能原因,强调本研究对该领域的意义以及后续研究需要注意的方面等.简要介绍下一步研究思路,进一步提出新问题,并对该领域的研究进行展望.
参考文献(References)(五号体&,TimesNewRoman加粗)
例:
[1]LiH,CaoW,XuY,etal.InflammatorypaininducedCBPexpressionchangeinrathippocampus[J].ChineseJournalofClinicalAnatomy(中国临床解剖学杂志,2016,29(5):546-549
[2]MalheirosJM,LimaM,AvanziRD,etal.Repetitivenoxiousneonatalstimuliincreasesdentategyruscellproliferationandhippocampalbrain-derivedneurotrophicfactorlevels[J].Hippocampus,2016,24(4):415-423
[3]韩刚,王以东,曹羽,等.直肠癌腹腔镜与开腹根治术的近远期疗效及安全性评估[J].现代生物医学进展,2016,13(8):1511-1513+1553
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英文模版()
AssociationStudyofHumanSerotonin5-HTR2AgenePolymorphismswithAlcoholDependenceinYunnanYiopulation*
YANGHao1,ZHONGShu-rong1,ZHAOLi-juan1,LIJin-hua1,ZENGXi-ran2,JINGQiang1△
(1KunmingMedicalUniversity,Kunming,Yunnan,650000,China,2UniversityofYork,Heslington,York,YO105DD,UK)
ABSTRACTObjective:Toinvestigatetherelationshipbetweenalcoholdependenceandpolymorphismofserotoninreceptor2a(5-HTR2A)geners6311inYunnanYipopulation.Methods:ThePCR-RFLPwasusedtoanalyzegeicpolymorphismof5-HT2ARgene,thegenotypeandgenefrequenciesin330controlgroupsand110ADgroups.Results:Twoallelesofthe5-HT2ARgeneweredetectedin440samples:allelesAandG,includingthreegenotypes:AA,AGandGG.Genotypefrequencywas30%,63.6%and6.4%inADgroups,and38.5%,55.8%and5.8%incontrolgroups,respectively.Conclusion:TherewasnosignificantassociationforHTR2Ageners6311betweenADgroupandcontrolgroupinYunnanYiPopulation.
Keywords:Alcoholdependence,HTR2A,Polymorphism,YunnanYipopulation
ChineseLibraryClassification(CLC):R394.3Documentcode:A
ArticleID:1673-6273
Introduction
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1MaterialsandMethods
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1.1Materials
详细说明研究对象(subject),包括:研究人员(subjects),性别(gender),年龄(age),物种(species),品种(breed),生理状态(physiologicalstate),微生物要说明菌株(strain),血
生物医学方面有关论文范文资料,与现代生物医学进展相关论文目录怎么自动生成参考文献资料: