技术参数 COVID-19/Influenza (A+B) /RSV Antigen Combo Rapid Test Kit is used for in vitro qualitative detection of novel coronavirus(COVID-19), influenza A/B virus and Respiratory Syncytial Virus (RSV) antigens in human nasal cavity and throat swab samples. Key Advantages • High Accuracy...
(BHQ-2); forward primer SARS-CoV-2 AgAgCTATgAATTgCAgAC; reverse primer SARS-CoV-2 gggAAATACAAAATTTggACA; fluorescent probe SARS-CoV-2 (FAM) -AATTggCAAAgAAATTTgACACCTTCA- (BHQ-1).;EFFECT: realizing the possibility of effective multiplex analysis for the diagnosis of influenza and COVID-...
Additionally, these patterns may vary over time as nonpharmaceutical COVID-19 interventions (e.g., social distancing, masking) are lessened, leading to a resurgence of other respiratory infections (e.g., influenza, respiratory syncytial virus) [18]. Third, the logistical challenges of enrolling ...
4月22日,万孚生物宣布其美国全资子公司Wondfo USA Co., Ltd.的三联检测试剂盒——新型冠状病毒、甲型流感病毒及乙型流感病毒三重检测试剂盒WELLlife COVID-19/Influenza A&B Test已经获得了美国食品和药物管理局(FDA)的紧急使用授权(EUA)。 此次授权标志着万孚生物在国际市场的影响力进一步增强,为公司在国际卫生领...
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Test Cassette: a test cassette includes the COVID-19 Antigen Test Strip and the Influenza A+B Test Strip, which are fixed inside a plastic device Extraction Reagent: Ampoule containing 0.4 mL of extraction reagent Sterilized Swab ...
Note: Co‑infection with influenza A, B and/or SARS‑CoV‑2 is possible. Test results are not intended to rule in or rule out other infections. Negative test result Test kit information Each kit contains 25 individually packaged, ready-to-use tests. ...
SARS-CoV-2 & Influenza A/B Multiplex Real-... StrongStep® SARS-CoV-2 & Influenza A/B Mult... Systeemapparaat foar SARS-CoV-2 & Influenza A... De nije coronaviruses hearre ta it β-genus... Dual Biosafety System Device foar SARS-CoV-2 Ant ... Bedoeld...
COVID-19/Influenza A+B Antigen Combo Rapid Test Kit (Colloidal gold method) COVID-19/Influenza A+B Antigen Combo Rapid Test Kit is used for in vitro qualitative detection of novel coronavirus(COVID-19) and influenza A/B virus antigens in human nasal ca
证券日报网讯 4月22日晚间,万孚生物发布公告称,公司美国全资子公司Wondfo USA Co.,Ltd(简称“美国子公司”)近日收到U.S.Food&Drug Administration(美国食品药品监督管理局,以下简称“FDA”)通知,美国子公司的新型冠状病毒、甲型流感病毒及乙型流感病毒三联检测试剂盒WELLlifeCOVID-19/Influenza A&B Test获得FDA的应...