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应用聚乙二醇沉淀比浊法检测水貂血清中循环免疫复合物的研究 被引量:3

Research of Detecting Circulating Immune Complexes in Mink Serum with polyethylene Glycol
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摘要 该项研究确立了聚乙二醇(PEG)沉淀比浊法,是检测水貂血清中循环免疫复合物(CIC)的理想方法。该方法的最适条件是:PEG浓度为5%;缓冲液浓度为0.1M,pH8.4;作用温度为4℃,作用时间为1h;室温20℃放置时间为30分钟。用该方法检测临床上健康、经阿留申病(AD)对流免疫电泳(CIEP)确认为阴性的水貂血清200份、阿留申病阳性水貂血清600份,其结果(OD值,X±SD)为:健康水貂0.034±0.023,阿留申病水貂0.241±0.152。经统计学处理,健康水貂与阿留申病貂的血清OD值之间,差异极显著(P<0.01),说明水貂AD的发病与CIC密切相关。PEG沉淀比浊法具有快速、简便、不需要特殊设备和重复性好等特点。 In this study, it was developed that polyethylene glycol(PEG) precipitation turbidimetry was th reasonable method for detecing the circuitingimmune complexes(CIC) in mink sera. This method was carried out throughkeeping the mixture of serum and 5% PEG(prepared with PH 8.4, 0.1Mborate buffer solution)for 1h at 4℃ and 0.5h at 20℃.The sera sample of 200 clinical healthy AD. CIEP negatiye minks and600 positiye minks with Aleutian disease was detected with t his method.The OD valuo (X±SD) of healthy minks was 0.034±0.023 and that of ADminks was 0.241±0.152.There was st gulf leant diffierence (p<0.01) betweenthe OD value of healthy minks and that of AD minks by statistical comparison.The result suggest that the CIC are closely Correlat ed to pat hogenesis of AD.PEG precipitat ion turbidimetry are rapid,simple, not needing specialequipment and good repeat ion. The development of this assay method issignificant to the research for pathogenesis mechanism and immune of ADin mink.
出处 《特产研究》 1994年第2期1-4,共4页 Special Wild Economic Animal and Plant Research
基金 "八五"农业部畜牧业重点科研专题 国家自然科学基金
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  • 1殷震,刘景华.动物病毒学[M]科学出版社,1985.

同被引文献23

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  • 2李月涛,霍金龙,信吉阁,曾养志.核酸疫苗的研究及应用进展[J].生物技术通报,2006,22(4):1-5. 被引量:10
  • 3彭宣宪.双特异性循环免疫复合物的研究进展[J].上海免疫学杂志,1996,16(5):315-317. 被引量:18
  • 4段义农,张耀娟,章子豪,侯敏,吴观陵.McAbDot-ELISA检测卫氏并殖吸虫循环免疫复合物[J].中国寄生虫病防治杂志,1997,10(1):34-36. 被引量:6
  • 5J.Ivan,N.Nagy,A.Magyar,I.Kacskovics,J.Meszaros.Functional restoration of the bursa of Fabricius following in ovo infectious bursal disease vaccination [J].Veterinary Immunology and Immunopathology,2001,79:235~248.
  • 6Semra Kurul,Salih Kavukcu,Banu Sis et al.Frequent vaccination and immune complex deposition in unilateral nephrectomized mice[J].Pediatr Nephrol,2004,19:621~626.
  • 7Brooke D.Humphrey,Chris C.Calvert,Kirk C.Klasing.The ratio of full length IgY to truncated IgY in immune complexes affects macrophage phagocytosis and the acutephage response of mallard ducks(Anas platyrhynchos)[J].Development and comparative immunology,2004,28:665~672.
  • 8Jeurissen,Janse,Lehrbach,Haddad,Avakian,Whitfil l.The working mechanism of an immune complex vaccine that protects chickens against infectious bursal disease [J].Immunology,1998,11(3):494~502.
  • 9Jeurissen,Janse,Lehrbach,Haddad,Avakian,Whitfil l.The working mechanism of an immune complex vaccine that protects chickens against infectious bursal disease [J].Immunology,1998,11(3):494~502.
  • 10曾祥伟,华育平,梁冬莹.水貂阿留申病毒VP2蛋白主要抗原表位基因原核表达及其检测应用[J].微生物学报,2007,47(6):1088-1090. 被引量:13

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