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首页> 外文期刊>Comparative Medicine >Mamu -DQA1 Allele and Genotype Frequencies in a Randomly Sampled Breeding Colony of Rhesus Macaques (Macaca mulatta)
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Mamu -DQA1 Allele and Genotype Frequencies in a Randomly Sampled Breeding Colony of Rhesus Macaques (Macaca mulatta)

机译:猕猴(Macaca mulatta)随机取样的繁殖群体中的Mamu -DQA1等位基因和基因型频率。

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Westudiedtheallelicandgenotypicdistributionofthemajorhistocompatibilityclass-IIlocusDQA1observedinarandomsampleofIndianrhesusmacaques(Macacamulatta)fromamajorbreedingfacilityintheUnitedStates.TheDNAwasisolatedfromwholebloodsamplescollectedbetween1991and1994from65Indianrhesusmonkeys.Polymerasechainreaction-restrictionfragmentlengthpolymorphismanalysis(PCR-RFLP),whichinvolvesuseofspecificamplificationofDQA1exon2andsubsequentrestrictiondigestionofthe242-basepairfragment,wasusedtogenotypetheanimalsforthe20knownmacaque(Mamu)-DQA1alleles.Frequenciesforfouralleles(DQA1*240x,*2502,*2503and*0102)differedsignificantlyfromthosereportedinasmallersampleofrhesusmacaquesfromtheGermanPrimateCenter.ThemodestgeneticsurveyofMamu-DQA1genotypespresentedherewillbeparticularlyusefulindesigningepidemiologicstudiesthatinvestigateassociationsbetweenimmunogeneticbackgroundanddiseasesusceptibilityinmacaquemodelsofhumandisease.
机译:Westudiedtheallelicandgenotypicdistributionofthemajorhistocompatibilityclass IIlocusDQA1observedinarandomsampleofIndianrhesusmacaques(Macacamulatta)fromamajorbreedingfacilityintheUnitedStates.TheDNAwasisolatedfromwholebloodsamplescollectedbetween1991and1994from65Indianrhesusmonkeys.Polymerasechainreaction restrictionfragmentlengthpolymorphismanalysis(PCR-RFLP),whichinvolvesuseofspecificamplificationofDQA1exon2andsubsequentrestrictiondigestionofthe242 basepairfragment,wasusedtogenotypetheanimalsforthe20knownmacaque(马目)-DQA1alleles.Frequenciesforfouralleles(DQA1 * 240X,2502,2503and 0102)differedsignificantlyfromthosereportedinasmallersampleofrhesusmacaquesfromtheGermanPrimateCenter.ThemodestgeneticsurveyofMamu DQA1genotypespresentedherewillbeparticularlyusefulindesigningepidemiologicstudiesthatinvestigateassociationsbetweenimmunogeneticbackgroundanddiseasesusceptibilityinmacaquemodelsofhumandisease。

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