〝西門子〞B型肝炎核心抗體檢驗試劑組

醫材分類

• B.4020分析特定試劑

醫器規格

#07566733#07569996:Quatity Control Material

限制項目

輸 入

適應症

利用化學冷光免疫分析法定性偵測人體血清或血漿中抗B型肝炎核心抗原之抗體。

醫材資訊

主成分

&#8226; Anti-HBc Total ReadyPack includes :\n(1) Lite Reagent 10.0 ml containing recombinant hepatitis B core antigen (~0.2μg/ml) labeled with acridinium ester in buffer with surfactant and preservatives.\n(2) Solid Phase 25.0 ml containing streptavidine coated paramagnetic microparticles preformed with biotinylated recombinant HBcAg (~0.2 μg/ml) in buffer with potassium thiocyanate (5.0%), bovine serum albumin,surfactant, and sodium azide (<0.1%).\n(3) Chaotrope Reagent 6.0 ml containing buffer with potassium thiocyanate (40%) and surfactant. \n(4) Ancillary Reagent 25.0 ml containing buffer with potassium thiocyanate (5.0%) and surfactant. \n(5) HBcT calibrator vials 7.0 ml/vial processed human plasma positive for HBc antibodies, bovine serum albumin, and preservatives.\n&#8226; HBcT quality control material 7.0 ml/vial containing processed human plasma negative and positive for \n anti-HBc with preservatives.\n

製造商

SIEMENS HEALTHCARE DIAGNOSTICS INC.

製造國

US

申請商

西門子醫療設備股份有限公司

有效日期

2030/03/03

發證日期

2010/03/03

供應藥局

目前尚無登錄供應此品項的藥局資料。