首页> 外国专利> SOLID-PHASE IMMUNO-ENZYME ANALYSIS (ELISA) FOR VASCULAR ENDOTHELIUM GROWTH FACTOR (VEGF)

SOLID-PHASE IMMUNO-ENZYME ANALYSIS (ELISA) FOR VASCULAR ENDOTHELIUM GROWTH FACTOR (VEGF)

机译:血管内皮生长因子(VEGF)的固相免疫酶分析(ELISA)

摘要

1. A method for detecting selective forms (VEGF110 +) of vascular endothelial growth factor (VEGF) in a biological sample, comprising the steps! (a) contacting and incubating the biological sample with a capture reagent immobilized on a solid support, wherein the capture reagent is an antibody that recognizes the same epitope as 5C3 anti-human VEGF antibody, wherein said monoclonal antibody specifically binds to residues in an amount of more than than 110, from human VEGF; ! (b) separating the biological sample from the immobilized capture reagents; ! (c) contacting the immobilized molecular complex of the capture-target reagent with a detectable antibody that binds to the VEGF domains responsible for binding to the KDR and / or FLT1 receptor, or which binds to an epitope in VEGF1-110; and! (d) measuring the level of VEGF110 + bound to capture reagents using a detection tool for a detectable antibody. ! 2. The method according to claim 1, where the biological sample is taken from a person. ! 3. The method according to claim 2, where the person is a patient with a vascular, diabetic or cancerous disease, and the measurement step (d) further comprises comparing with a standard curve to determine the level of VEGF in comparison with the level in a healthy individual. ! 4. The method according to claim 1, where the biological sample is a tumor lysate, plasma, serum or urine. ! 5. The method according to claim 1, where the capture reagent is a 5C3 monoclonal antibody. ! 6. The method according to claim 1, where the immobilized capture reagents are applied as a coating on a microtiter plate. ! 7. The method according to claim 1, where the detected antibody is directly �
机译:1.一种检测生物样品中血管内皮生长因子(VEGF)的选择性形式(VEGF110 +)的方法,包括以下步骤! (a)将生物样品与固定在固体支持物上的捕获试剂接触并孵育,其中捕获试剂是与5C3抗人VEGF抗体识别相同表位的抗体,其中所述单克隆抗体以一定量特异性结合残基来自人类VEGF的超过110; ! (b)从固定的捕获剂中分离出生物样品; ! (c)使捕获目标试剂的固定分子复合物与可检测抗体接触,该可检测抗体与负责与KDR和/或FLT1受体结合的VEGF域结合,或与VEGF1-110中的表位结合;和! (d)使用可检测抗体的检测工具测量与捕获剂结合的VEGF110 +的水平。 ! 2.根据权利要求1所述的方法,其中,所述生物样品是从人身上获取的。 ! 3.根据权利要求2所述的方法,其中,所述人是患有血管,糖尿病或癌性疾病的患者,并且所述测量步骤(d)进一步包括与标准曲线比较以确定VEGF水平,所述VEGF水平与糖尿病患者的水平相比较。一个健康的人。 ! 4.根据权利要求1所述的方法,其中所述生物样品是肿瘤裂解物,血浆,血清或尿液。 ! 5.根据权利要求1的方法,其中所述捕获试剂是5C3单克隆抗体。 ! 6.根据权利要求1的方法,其中将固定的捕获试剂作为涂层施加在微量滴定板上。 ! 7.根据权利要求1所述的方法,其中,所检测的抗体是直接的。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号