BioReagent 级 ，适用于对基线干扰要求严格的色谱和分析工作流程。
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在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
巨噬细胞炎性蛋白1α(MIP-1α;CCL3)是属于CC趋化因子家族的一种细胞因子，在急性炎症状态下通过与受体CCR1、CCR4和CCR5结合，参与多形核白细胞的招募和激活。它产生一种快速发作的单相发热，其程度等于或大于用重组人肿瘤坏死因子或重组人白细胞介素-1产生的发热。它可能参与了不通过前列腺素合成介导的发热反应，而且临床上不能被环氧化酶消减。CCL3已被证明与CCL4相互作用，吸引巨噬细胞、单核细胞和中性粒细胞。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人巨噬细胞炎性蛋白1α(MIP-1α;CCL3)捕获抗体的微孔中，依次加入样本、标准品、生物素标记的检测抗体，HRP酶结合物，中间经过温育和洗涤，用底物TMB显色，TMB在过氧化物酶(HRP)的催化下转化成蓝色，并在酸的作用下转化成最终的黄色。颜色的深浅和样本中的人巨噬细胞炎性蛋白1α(MIP-1α;CCL3)呈正相关。用酶标仪在450nm 波长下测定吸光度（OD值），计算样本浓度。
This kit employs the sandwich enzyme-linked immunosorbent assay (ELISA) principle. Microplate wells are pre-coated with a capture antibody specific to Human MIP-1α;CCL3. Following this, the sample, standards, a biotin-conjugated detection antibody, and an HRP (horseradish peroxidase)-labeled conjugate are added sequentially to the wells. The procedure involves incubation and wash steps between each addition. For detection, TMB substrate is used. TMB yields a blue color in the presence of the peroxidase activity of HRP. The reaction is then stopped with an acid solution, which converts the blue color to a final yellow color. The intensity of the yellow color is directly proportional to the concentration of Human MIP-1α;CCL3 present in the sample. The optical density (OD) is measured at a wavelength of 450 nm using a microplate reader. Finally, the concentration of the target analyte in the sample is calculated based on the standard curve generated from the standards.
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