“詩干地巴底”促腎上腺皮質刺激素放射免疫分析試劑
“Scantibodies” ACTH IRMA Assay

適應症
定量檢測人體血漿中隻促腎上腺皮質刺激素(ACTH)的含量。  
劑型
 
包裝
#3KG011：100 tubes 
許可證字號
衛部藥製字第018425號 
註銷狀態
1 
註銷日期
2019-12-20  
註銷理由
851 
有效日期
2017-09-13  
發證日期
2007-09-13  
許可證種類
09 
中文品名
“詩干地巴底”促腎上腺皮質刺激素放射免疫分析試劑 
英文品名
“Scantibodies” ACTH IRMA Assay 
藥品類別
A 臨床化學及臨床毒理學 
申請商名稱
泰歷藥品儀器股份有限公司  
申請商地址
台北市大同區承德路二段81號15樓 
通關簽審文件編號
DHAS0601842507 
資料更新時間
 
製造商
名稱 廠址 公司地址 國別 製程
SCANTIBODIES LABORATORY, INC. 9336 ABRAHAM WAY, SANTEE, CA 92071, U.S.A. US
成份表
處方標示 成分名稱 含量 單位
1 1.ACTH Standards：One set of standards consists of seven vials containing lyophilized serum with synthetic ACTH peptide.\n2.ACTH Controls：One set of controls consists of two vials containing ACTH in lyophilized serum with 0.1% (w/v) sodium azide.\n3.ACTH 125I-Antibody：One set of tracer consists of two bottles of 125I-anti ACTH (24-39). Each bottle contains polyclonal goat anti ACTH (24-39) antibody which is labeled with 125I and dissolved in 5 ml phosphate buffered saline with sodium azide 0.1% (w/v) and protein stabilizers. The maximum radioactivity in a bottle is <370 kBq (<10μCi).\n4.ACTH Antibody Coated Tubes：2 packages of 100 polystyrene tubes (12 x 75 mm diameter) plus desiccant. The tubes are coated with goat anti-ACTH (1-16) antibody. The desiccant contains silica.\n5.Wash Concentrate：One bottle contains 30 ml of 30 fold concentrate of phosphate buffered saline with sodium azide 1.5% (w/v) and detergent.\n