AffiniPure Goat jackson现货

AffiniPure Goat jackson现货

用免疫亲和层析法从抗血清中分离出完整的IgG抗体。它们有一个FC部分和两个抗原结合的Fab部分，由二硫键连接在一起，因此它们是二价的。平均分子量约为160 kDa。抗体的整体IgG形式适用于大多数免疫检测程序，是有效的。

根据免疫电泳和/或ELISA方法，抗体与人IgG重链的Fc部分发生反应，而与人IgG的Fab部分无反应。未检测到抗人IgM、IgA或非免疫球蛋白血清蛋白的抗体.。该抗体已通过ELISA和/或固相吸附试验，以确保与牛、马和小鼠血清蛋白的zui低交叉反应，但它可能与其他物种的免疫球蛋白发生交叉反应。

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent. The average molecular weight is reported to be about 160 kDa. The whole IgG form of antibodies is suitable for the majority of immunodetection procedures and is the most cost effective.

Based on immunoelectrophoresis and/or ELISA, the antibody reacts with the Fc portion of human IgG heavy chain but not with the Fab portion of human IgG. No antibody was detected against human IgM or IgA, or against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse and mouse serum proteins, but it may cross-react with immunoglobulins from other species.

用免疫亲和层析法从抗血清中分离出完整的IgG抗体。它们有一个FC部分和两个抗原结合的Fab部分，由二硫键连接在一起，因此它们是二价的。平均分子量约为160 kDa。抗体的整体IgG形式适用于大多数免疫检测程序，是有效的。

根据免疫电泳和/或ELISA方法，抗体与人IgG重链的Fc部分发生反应，而与人IgG的Fab部分无反应。未检测到抗人IgM、IgA或非免疫球蛋白血清蛋白的抗体.。该抗体已通过ELISA和/或固相吸附试验，以确保与牛、马和小鼠血清蛋白的zui低交叉反应，但它可能与其他物种的免疫球蛋白发生交叉反应。

AffiniPure Goat jackson现货

AffiniPure Goat jackson现货

AffiniPure Goat jackson现货

AffiniPure Goat jackson现货

AffiniPure Goat jackson现货