GMP Human TNF-alpha Protein (Cat. No. GMP-TNAH23) is expressed in human 293 cells (HEK293) and comprises amino acids Val 77 to Leu 233 (Accession # P01375). This protein has no "tag". It has a ...
GMP Human FGF Basic Protein was analyzed by SDS-PAGE under reducing (R) conditions. The gel was stained with Coomassie Blue, confirming a purity of greater than 95 %. GMP Human FGF Basic Protein (Cat.
2023年是东方生物在动保领域布局的关键一年。东方生物于当年底获得了新版《中华人民共和国兽药GMP证书》《中华人民共和国兽药生产许可证》,可开展动宠物免疫学类诊断制品(B类)的生产。当年,公司通过收购北京华信农威生物科技,获取涵盖猪蓝耳病灭活疫苗、猪 ...
(NASDAQ:APDN) ("Applied DNA" or the "Company"), a leader in PCR-based DNA technologies, today announced the completion of the buildout of its new Good Manufacturing Practices (GMP) manufacturing ...
Quality Power IPO: Apply or not? Choice Broking adds a 'subscribe' tag to the book build issue: "At the upper price band, QPEEL is demanding an EV/S multiple of 5.9x, which is at a discount to ...
Quality Power IPO subscription status: Quality Power Electrical Equipments' initial public offering (IPO), which opened for public subscription on February 14, 2025, is set to conclude today, February ...
近期,IVD行业的AI概念股表现强势。安必平、迪安、华大、三诺、万孚、润达、金域、塞力医疗等多家IVD企业股价大幅上涨。 这一轮强势表现离不开 ...
5] Quality Power IPO lot size: A bidder can apply in lots, and one lot of the public issue compares 26 company shares. 7] Quality Power IPO allotment date: The most likely date for share allotment ...
The revised Schedule M establishes enhanced quality standards and Good Manufacturing Practices (GMP) for pharmaceutical manufacturers, aiming to improve overall manufacturing quality, safety, and ...
体外诊断(IVD)是指在人体之外通过对人体样本(如血液、体液、组织等)进行检测而获取临床诊断信息产品和服务,目前已经成为疾病预防、诊断 ...
红细胞叶酸检测仪在临床使用前的办理流程涉及多个环节和法规要求,以下是对该流程的概述: 一、了解法规要求 首先,需要深入了解目标市场(如中国、欧盟、美国等)关于体外诊断试剂(IVD)的法规、标准 ... 如ISO 13485或GMP证书,以及相关的质量手册、程序 ...
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