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使用酶免疫测定法检测凝血因子IX抗原

Assay of factor IX antigen using an enzyme immuno assay.

作者信息

Parquet-Gernez A, Mazurier C, Amiral J, Martinoli J L

出版信息

Thromb Res. 1984 Sep 15;35(6):703-12. doi: 10.1016/0049-3848(84)90273-1.

DOI:10.1016/0049-3848(84)90273-1
PMID:6506026
Abstract

An Enzyme Linked immuno Sorbent Assay (ELISA) was developed for the measurement of factor IX:Ag. The results obtained in 90 control subjects, 56 hemophilia B patients and 40 patients under oral anticoagulant treatment were compared with factor IX:C and factor IX:Ag levels according to Electro Immuno-Assay (EIA). In healthy volunteers the mean factor IX:C level was 106.7 U/dl, the mean factor IX:Ag level was 96.8 U/dl according to EIA procedure and 101.5 U/dl according to ELISA method. Using ELISA, 10 hemophiliacs had no detectable antigen, and 13 had minute amounts of IX:Ag. All these patients are classified as B-. Among the others 21 had reduced antigen and are considered as BR and 12 had normal level of IX:Ag and are B+. Patients taking oral anticoagulants had not only a decreased factor IX:C level but also a reduced factor IX:Ag level which is always lower when using EIA procedure in the presence of EDTA than according to ELISA method.

摘要

开发了一种酶联免疫吸附测定法(ELISA)用于测量凝血因子IX:抗原。将90名对照受试者、56名B型血友病患者和40名接受口服抗凝治疗的患者的检测结果,与采用电免疫测定法(EIA)测得的凝血因子IX:C和凝血因子IX:抗原水平进行比较。在健康志愿者中,根据EIA程序,凝血因子IX:C的平均水平为106.7 U/dl,凝血因子IX:抗原的平均水平为96.8 U/dl;根据ELISA方法,凝血因子IX:抗原的平均水平为101.5 U/dl。使用ELISA法检测时,10名血友病患者检测不到抗原,13名患者有微量的IX:抗原。所有这些患者被归类为B-型。其他患者中,21名患者抗原减少,被认为是BR型,12名患者IX:抗原水平正常,为B+型。服用口服抗凝剂的患者不仅凝血因子IX:C水平降低,凝血因子IX:抗原水平也降低,在存在乙二胺四乙酸(EDTA)的情况下,使用EIA程序检测时其水平总是低于ELISA方法检测的结果。

相似文献

1
Assay of factor IX antigen using an enzyme immuno assay.使用酶免疫测定法检测凝血因子IX抗原
Thromb Res. 1984 Sep 15;35(6):703-12. doi: 10.1016/0049-3848(84)90273-1.
2
Sensitive solid phase enzyme immunoassay for factor IX antigen and classification of hemophilia B.用于因子IX抗原的敏感固相酶免疫测定及B型血友病的分类
Haemostasis. 1983;13(1):9-16. doi: 10.1159/000214698.
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Immunologic studies of factor IX (Christmas factor). II. Immunoradiometric assay of factor IX antigen.
Br J Haematol. 1978 Jun;39(2):215-24. doi: 10.1111/j.1365-2141.1978.tb01091.x.
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Studies on immunological assay of vitamin-K dependent factors. III. A double monoclonal immunoradiometric assay for factor IX antigen.
Br J Haematol. 1986 Mar;62(3):513-24. doi: 10.1111/j.1365-2141.1986.tb02963.x.
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Prenatal diagnosis of hemophilia B by an immunoradiometric assay of factor IX.
Blood. 1980 Sep;56(3):397-401.
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Rabbit polyclonal antibodies against the calcium-dependent conformation of factor IX and their application in solid phase immunoradiometric assays.
Thromb Haemost. 1986 Feb 28;55(1):122-8.
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An agarose plate method for detecting alloantisera to coagulant factor IX and factor IX antigen.一种检测凝血因子IX同种异体抗血清和因子IX抗原的琼脂糖平板法。
Br J Haematol. 1980 Feb;44(2):313-21. doi: 10.1111/j.1365-2141.1980.tb01214.x.
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Immunoassays of factor IX antigen using monoclonal antibodies.
Br J Haematol. 1985 Feb;59(2):265-75. doi: 10.1111/j.1365-2141.1985.tb02993.x.
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Immunological heterogeneity of haemophilia B: a multicentre study of 98 kindreds.
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A simple method for detection of human factor IX inhibitor using ELISA.一种使用酶联免疫吸附测定法检测人凝血因子IX抑制物的简单方法。
Scand J Clin Lab Invest. 1997 Dec;57(8):683-8. doi: 10.3109/00365519709105229.

引用本文的文献

1
T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detection.
Hum Genet. 1991 Jul;87(3):333-7. doi: 10.1007/BF00200915.
2
Missense mutations and the magnitude of functional deficit: the example of factor IX.
Hum Genet. 1992 May;89(3):295-7. doi: 10.1007/BF00220543.