• 我要登录|
  • 免费注册
    |
  • 我的丁香通
    • 企业机构:
    • 成为企业机构
    • 个人用户:
    • 个人中心
  • 移动端
    移动端
丁香通 logo丁香实验_LOGO
搜实验

    大家都在搜

      大家都在搜

        0 人通过求购买到了急需的产品
        免费发布求购
        发布求购
        点赞
        收藏
        wx-share
        分享

        Radioligand Binding Assay

        互联网

        1070
        Characterization and cloning of the AT1 and AT2 receptors would not have been possible without an assay that could detect and measure the density and affinity of these receptors. The most frequently used, if not the only, methodological approach used to investigate these receptors is the radioligand binding assay performed either in a test tube with tissue-membrane preparations or cultured cells, or on tissue sections (the latter revealed by autoradiography). This chapter will only deal with the test-tube radioligand binding assay. In this assay, a radiolabeled ligand (labeled with 125 I or 3 H, for example) is incubated with a membrane preparation or cells in presence of receptor subtype-specific antagonist or agonist. After reaching equilibrium, the receptor-bound tracer is separated from the free tracer by rapid filtration through glass fiber filters or by centrifugation. The amount (cpm) of bound tracer is then used to calculate the density and affinity of each receptor subtype. Alternatively, other experiments can be designed to derive kinetics of association and dissociation or saturation.
        ad image
        提问
        扫一扫
        丁香实验小程序二维码
        实验小助手
        丁香实验公众号二维码
        扫码领资料
        反馈
        TOP
        打开小程序