碧云天生产的碱性磷酸酶检测试剂盒 (Alkaline Phosphatase Assay Kit)是一种用于快速、便捷地检测细胞或组织样品的裂解或匀浆产物的上清液、血清、血浆、尿液等样品中内源性的碱性磷酸酶活性的试剂盒。 碱性磷酸酶 (Alkaline Phosphatase, AP/ALP/AKP/ALKP/ALPase/Alk Phos)也称碱性磷酸酯酶 (EC 3.1.3.1)，可以在碱性条件下催化磷酸酯键的水解。 哺乳动物中，肝脏、胆管、肾脏、骨头和胎盘中的碱性磷酸酶活性比较高。

Alkaline phosphatase (ALP) assay kit (Single reagent, IFCC recommendation method). Cat# MBS2540469.

碱性磷酸酶（ALP）活性的变化与一系列生理和病理事件紧密关联， 比如骨骼发育、骨骼相关疾病、妊娠相关疾病和炎症性肠病（inflammatory bowel diseases）等。正因如此，ALP被用作衡量生理特征或疾病的参照指标。

Investigation of hepatobiliary or bone disease. Increased levels in liver disease (particularly in association with cholestasis), bone disease (with increased osteoblastic activity eg, Paget's disease), some bony metastases (especially prostate and breast), and at times in malignancy without liver or bone metastases (Regan isoenzyme).

2015年6月15日 · Herein, we fabricated a kind of bi-MBs by co-immobilizing antibody and ALP signal molecules on magnetic nanobead surface. The bi-MBs were used not only as separation and enrichment carriers but also as signal carriers, which greatly enhanced target capture efficiency, simplified immunoreaction and improved detection sensitivity.

血清肝酶，包括谷丙转氨酶（alt）、谷草转氨酶（ast）、碱性磷酸酶（alp）、谷氨酰转肽酶（ggt），被认为是临床评估肝损伤的重要标志物 [1]。 不同地区，不同性别的人群间血清肝酶存在差异，我国多中心研究数据显示…

西宝生物创新研发团队依托现有技术平台自主研发生产的alp碱性磷酸酶产品，性能稳定、活性高，可替代进口品牌，且经众多客户的反复测评得到了大家的一致认可。此酶在化学发光平台经过多个临床项目验证，信噪比、精密度、稳定性等与进口品牌性能持平。

This ELISA kit applies to the in vitro quantitative determination of Chicken ALP concentrations in serum, plasma and other biological fluids. Specification Sensitivity: 0.47ng/mL. Detection Range: 0.78-50ng/mL Specificity: This kit recognizes Chicken ALP in samples. No significant cross-reactivity or interference between

Rat alkaline phosphatase(ALP)ELISA Kit Cat.No: MBS3808039 Storage：2-8°°C. validity：six months. The sensitivity by this assay is 0.1ng/mL Standard concentration was followed by: 20,10,5,2.5,1.25,0ng/mL Both intra-assay CV and inter-assay CV is less than 15%. Intended use

2025年2月1日 · In the presence of S. aureus, the secreted MNase preferentially cut the nucleobase AT-rich regions of DNA sequences on magnetic beads (MBs) to release alkaline phosphatase (ALP), which subsequently mediated the oxTMB reduction for inducing the colorimetric/SERS signal fade away.