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分泌视黄酸特异性单克隆抗体的杂交瘤细胞系的制备。

Production of a hybridoma cell line secreting retinoic acid-specific monoclonal antibody.

作者信息

Zhou H R, Abouzied M M, Zile M H

机构信息

Department of Food Science and Human Nutrition, Michigan State University, East Lansing 48824-1224.

出版信息

J Immunol Methods. 1991 Apr 25;138(2):211-23. doi: 10.1016/0022-1759(91)90169-g.

Abstract

A stabilized hybridoma cell line secreting anti-retinoic acid monoclonal antibodies of subclass IgG1 with kappa chains was produced by fusing NS-1 myeloma cells with the spleen cells from BALB/c female mice immunized with all-trans-4-oxoretinoic acid-oxime-chicken IgG conjugate. The antibody titer of mice ascitic fluid ranged from 1/12,800 to 1/25,600, as determined by competitive indirect enzyme-linked immunosorbent assay (ELISA). 50% inhibition dosage of all-trans-retinoic acid at a 1/20,000 dilution of mice ascitic fluid was 6.6 ng/ml, as determined by ELISA. The anti-retinoic acid monoclonal antibody was generated in mice ascitic fluid and purified by protein G affinity chromatography. Cross-reactivity of the monoclonal antibody was determined at 0.1 microgram/ml concentration of retinoids and indicated high specificity to both all-trans-retinoic acid (86% inhibition) and 13-cis-retinoic acid (87% inhibition), and strong cross-reactivity with 4-oxoretinoic acid (77%) and 4-oxoretinoic acid oxime (109%). Specificity was confirmed by the horseradish peroxidase-linked immunostaining method and immunoradioassay. The affinity constant of the monoclonal antibody, K, was determined to be 3.6 X 10(9) l/mol. A calibration curve for retinoic acid using the monoclonal antibody to retinoic acid was developed; the detection limit for all-trans-retinoic acid is 1 ng/ml in the competitive indirect ELISA. The antibody counteracts the effect of retinoic acid on growth inhibition and differentiation in HL-60 cells.

摘要

通过将NS-1骨髓瘤细胞与用全反式-4-氧代视黄酸肟-鸡IgG偶联物免疫的BALB/c雌性小鼠的脾细胞融合,产生了一种稳定的杂交瘤细胞系,该细胞系分泌具有κ链的IgG1亚类抗视黄酸单克隆抗体。通过竞争性间接酶联免疫吸附测定(ELISA)测定,小鼠腹水的抗体效价范围为1/12,800至1/25,600。通过ELISA测定,小鼠腹水1/20,000稀释液中全反式视黄酸的50%抑制剂量为6.6 ng/ml。抗视黄酸单克隆抗体在小鼠腹水中产生,并通过蛋白G亲和层析纯化。在0.1微克/毫升的类视黄醇浓度下测定单克隆抗体的交叉反应性,结果表明其对全反式视黄酸(86%抑制)和13-顺式视黄酸(87%抑制)具有高特异性,与4-氧代视黄酸(77%)和4-氧代视黄酸肟(109%)具有强交叉反应性。通过辣根过氧化物酶标记的免疫染色法和免疫放射测定法确认了特异性。单克隆抗体的亲和常数K被测定为3.6×10(9) l/mol。利用抗视黄酸单克隆抗体建立了视黄酸的校准曲线;在竞争性间接ELISA中,全反式视黄酸的检测限为1 ng/ml。该抗体可抵消视黄酸对HL-60细胞生长抑制和分化的作用。

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