AffiniPure Goat jackson現貨

AffiniPure Goat jackson現貨

用免疫親和層析法從抗血清中分離出完整的IgG抗體。它們有一個FC部分和兩個抗原結合的Fab部分，由二硫鍵連接在一起，因此它們是二價的。平均分子量約為160 kDa。抗體的整體IgG形式適用于大多數免疫檢測程序，是有效的。

根據免疫電泳和/或ELISA方法，抗體與人IgG重鏈的Fc部分發生反應，而與人IgG的Fab部分無反應。未檢測到抗人IgM、IgA或非免疫球蛋白血清蛋白的抗體.。該抗體已通過ELISA和/或固相吸附試驗，以確保與牛、馬和小鼠血清蛋白的zui低交叉反應，但它可能與其他物種的免疫球蛋白發生交叉反應。

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.

用免疫親和層析法從抗血清中分離出完整的IgG抗體。它們有一個FC部分和兩個抗原結合的Fab部分，由二硫鍵連接在一起，因此它們是二價的。平均分子量約為160 kDa。抗體的整體IgG形式適用于大多數免疫檢測程序，是有效的。

根據免疫電泳和/或ELISA方法，抗體與人IgG重鏈的Fc部分發生反應，而與人IgG的Fab部分無反應。未檢測到抗人IgM、IgA或非免疫球蛋白血清蛋白的抗體.。該抗體已通過ELISA和/或固相吸附試驗，以確保與牛、馬和小鼠血清蛋白的zui低交叉反應，但它可能與其他物種的免疫球蛋白發生交叉反應。

AffiniPure Goat jackson現貨

AffiniPure Goat jackson現貨

AffiniPure Goat jackson現貨

AffiniPure Goat jackson現貨

AffiniPure Goat jackson現貨