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使用商业抗血清测定VIII因子相关抗原。

Determination of factor VIII-related antigen using commercial antisera.

作者信息

Chediak J, Maxey B, Telfer M

出版信息

Am J Clin Pathol. 1977 May;67(5):462-9. doi: 10.1093/ajcp/67.5.462.

DOI:10.1093/ajcp/67.5.462
PMID:404869
Abstract

Commercially available antiserum to factor VIII was used in several tests to determine whether it might serve as a reference between research laboratories involved in investigation of the factor VIII complex and whether the antiserum might be useful in the screening of large populations of patients with hereditary disorders of factor VIII. In Ouchterlony plates, the antiserum gave a single line of identity with concentrated factor VIII, cryoprecipitate, and human plasma. The antiserum was capable of inhibiting the ristocetin response of normal platelets. Testing antigenic factor VIII by the Laurell technic with the commercial antiserum on plasmas from normal and stressed normal controls, patients with von Willebrand's disease, patients with hemophilia A, and obligate carriers of hemophilia A gave diagnostic and reproducible results.

摘要

使用市售的抗凝血因子VIII抗血清进行了多项测试,以确定其是否可作为参与凝血因子VIII复合物研究的各研究实验室之间的参考标准,以及该抗血清是否有助于筛查大量患有遗传性凝血因子VIII疾病的患者。在欧氏免疫扩散板试验中,该抗血清与浓缩凝血因子VIII、冷沉淀物及人血浆形成一条单一的沉淀线。该抗血清能够抑制正常血小板的瑞斯托霉素反应。运用劳雷尔技术,以该市售抗血清检测正常及应激状态下的正常对照者、血管性血友病患者、甲型血友病患者及甲型血友病基因携带者血浆中的抗原性凝血因子VIII,得出了具有诊断价值且可重复的结果。

相似文献

1
Determination of factor VIII-related antigen using commercial antisera.使用商业抗血清测定VIII因子相关抗原。
Am J Clin Pathol. 1977 May;67(5):462-9. doi: 10.1093/ajcp/67.5.462.
2
Platelet-bound ristocetin aggregation factor in normal subjects and patients with von Willebrand's disease.正常受试者及血管性血友病患者血小板结合的瑞斯托菌素聚集因子
J Lab Clin Med. 1976 Jun;87(6):976-86.
3
Acquired von Willebrand syndrome with inhibitors both to factor VIII clotting activity and ristocetin-induced platelet aggregation.获得性血管性血友病综合征,同时伴有针对凝血因子VIII凝血活性和瑞斯托霉素诱导的血小板聚集的抑制剂。
Br J Haematol. 1976 Aug;33(4):565-73. doi: 10.1111/j.1365-2141.1976.tb03575.x.
4
Re-evaluation of plasmas from patients previously diagnosed as having von Willebrand's disease with the factor VIII-related antigen and ristocetin cofactor assay.通过因子VIII相关抗原和瑞斯托霉素辅因子测定法对先前诊断为血管性血友病患者的血浆进行重新评估。
Am J Clin Pathol. 1979 Jan;71(1):26-30. doi: 10.1093/ajcp/71.1.26.
5
Dissociation between factor VIII (activity and antigen) and ristocetin-induced platelet aggregation in von Willebrand's disease.血管性血友病中因子VIII(活性与抗原)及瑞斯托霉素诱导的血小板聚集之间的解离
Acta Haematol. 1975;53(1):44-8. doi: 10.1159/000208154.
6
Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。
J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.
7
Electrophoretic heterogeneity of normal factor VIII/Von Willebrand protein, and abnormal electrophoretic mobility in patients with Von Willebrand's disease.正常因子VIII/血管性血友病因子蛋白的电泳异质性,以及血管性血友病患者的异常电泳迁移率。
J Lab Clin Med. 1976 Feb;87(2):185-94.
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Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.血管性血友病中瑞斯托霉素诱导的血小板聚集缺陷及其通过因子VIII的纠正。
J Clin Invest. 1973 Nov;52(11):2697-707. doi: 10.1172/JCI107464.
9
Detection of heterozygotes in both parents of homozygous patients with Von Willebrand's disease.检测血管性血友病纯合子患者双亲中的杂合子。
J Clin Pathol. 1975 Apr;28(4):309-16. doi: 10.1136/jcp.28.4.309.
10
Infusion of human and canine factor VIII in dogs with von Willebrand's disease: studies of the von Willebrand and factor VIII synthesis stimulating factors.
Scand J Haematol. 1976 Oct;17(4):263-75. doi: 10.1111/j.1600-0609.1976.tb01184.x.