• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

In vitro characterization of antithrombin III concentrates--a single-blind study.

作者信息

Hellstern P, Moberg U, Ekblad M, Anders C U, Faller B, Müller S

机构信息

Institute of Transfusion Medicine and Immunohematology, Klinikum Ludwigshafen am Rhein, Germany.

出版信息

Haemostasis. 1995 Jul-Aug;25(4):193-201. doi: 10.1159/000217160.

DOI:10.1159/000217160
PMID:7557658
Abstract

Twenty-three lots of five antithrombin III (AT III) concentrates from four manufacturers were analyzed in a single-blind study. All the preparations had been virus-inactivated by pasteurization, and one concentrate had also been treated with solvent/detergent (S/D). AT III activities were determined using two thrombin-based and one factor Xa-based chromogenic substrate assays. AT III antigen was measured by kinetic nephelometry. All AT III assays were tested against the first international reference preparation coded 72/1. In addition, AT III was characterized by crossed immunoelectrophoresis in the presence of heparin and by gel filtration. The following were quantified: heparin cofactor II activity and antigen content, heparin activity, thrombin-AT III complexes, AT III-protease complexes, total protein, albumin, immunoglobulins, glucose and pH. The AT III concentrates differed markedly in terms of their purity and potency. The specific activities of AT III and the ratios of AT III activity to antigen content ranged from 3.4 to 6.9 and from 0.63 to 0.84, respectively. The highest values were found in five lots of the concentrate that had been treated by both pasteurization and S/D. This preparation was the only one that was virtually free of denaturated AT III, as judged by crossed immunoelectrophoresis. Marked batch-to-batch variation in AT III potencies was found in two out of the five preparations analyzed. In two out of five lots from one manufacturer, the measured potencies were more than 10% lower than the declared potencies.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

相似文献

1
In vitro characterization of antithrombin III concentrates--a single-blind study.
Haemostasis. 1995 Jul-Aug;25(4):193-201. doi: 10.1159/000217160.
2
Studies of the heterogeneity of antithrombin III concentrates.
Br J Haematol. 1983 Sep;55(1):37-46. doi: 10.1111/j.1365-2141.1983.tb01222.x.
3
Residues Tyr253 and Glu255 in strand 3 of beta-sheet C of antithrombin are key determinants of an exosite made accessible by heparin activation to promote rapid inhibition of factors Xa and IXa.抗凝血酶β-折叠C的第3条链中的酪氨酸253和谷氨酸255残基是一个外位点的关键决定因素,该外位点通过肝素激活变得可及,以促进对因子Xa和IXa的快速抑制。
J Biol Chem. 2006 May 12;281(19):13424-13432. doi: 10.1074/jbc.M600415200. Epub 2006 Mar 3.
4
Homozygous variant of antithrombin III that lacks affinity for heparin, AT III Kumamoto.抗凝血酶III的纯合变体,对肝素缺乏亲和力,即熊本抗凝血酶III。
Thromb Haemost. 1989 Feb 28;61(1):20-4.
5
Purification and characterization of hereditary abnormal antithrombin III with impaired thrombin binding.凝血酶结合受损的遗传性异常抗凝血酶III的纯化与特性分析
J Lab Clin Med. 1984 Aug;104(2):245-56.
6
Characterization of an abnormal antithrombin (Milano 2) with defective thrombin binding.
Thromb Haemost. 1986 Dec 15;56(3):349-52.
7
Abnormal antithrombin III with defective serine protease binding (antithrombin III "Denver").具有缺陷性丝氨酸蛋白酶结合能力的异常抗凝血酶III(抗凝血酶III“丹佛型”)
J Clin Invest. 1986 Mar;77(3):887-93. doi: 10.1172/JCI112386.
8
Preparation and characterization of monoclonal antibodies against the human thrombin-antithrombin III complex.抗人凝血酶 - 抗凝血酶III复合物单克隆抗体的制备与表征
Biochim Biophys Acta. 1988 Jan 4;952(1):37-47. doi: 10.1016/0167-4838(88)90099-4.
9
The allosteric mechanism of activation of antithrombin as an inhibitor of factor IXa and factor Xa: heparin-independent full activation through mutations adjacent to helix D.抗凝血酶作为因子 IXa 和因子 Xa 抑制剂的变构激活机制:通过紧邻 D 螺旋的突变实现肝素非依赖性完全激活。
J Biol Chem. 2013 Nov 22;288(47):33611-33619. doi: 10.1074/jbc.M113.510727. Epub 2013 Sep 25.
10
Crossed immunoelectrophoresis as applied to studies on complex formation. The binding of heparin to antithrombin III and the antithrombin III--thrombin complex.应用于复合物形成研究的交叉免疫电泳。肝素与抗凝血酶III的结合以及抗凝血酶III - 凝血酶复合物
J Immunol Methods. 1977;14(3-4):271-81. doi: 10.1016/0022-1759(77)90138-7.