Glycylproline dipeptidyl peptidase detection reagent kit (rate method) - NMPA Registration 冀械注准20142400365
Access comprehensive regulatory information for Glycylproline dipeptidyl peptidase detection reagent kit (rate method) in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 冀械注准20142400365 and owned by Langfang Hengyi Biotechnology Co., Ltd.. The device was approved on November 07, 2019.
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For in vitro quantitative determination of glycylproline dipeptide aminopeptidase activity in serum or urine.
用于体外定量测定血清或尿液中甘氨酰脯氨酸二肽氨基肽酶的活性。
Reagent 1: Diglycinopeptide, 8.32 g/L; Trihydroxyaminomethane (Tris), 8.5g/L; Reagent 2: sodium azide, 1 g/L; Glycylproline p-nitroaniline, 1.62 g/L.
试剂1：双甘肽，8.32g/L ； 三羟基氨基甲烷（Tris）， 8.5g/L；试剂2：叠氮钠，1g/L ； 甘氨酰脯氨酸对硝基苯胺，1.62g/L。