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产地 | 进口 | 规格 | 48T |
---|---|---|---|
级别 | 化工级 | 证书 | ISO系列证书 |
编号SEA861Hu
物种Homo sapiens (Human,人) 相同的名称,不同的物种。
实验方法双抗夹心
反应时长3h
检测范围7.8-500ng/mL
灵敏度z小可检测剂量小于等于3.7ng/mL.
样本类型serum, plasma and other biological fluids
下载英文说明书 中文说明书
规格48T96T 96T*5 96T*10 96T*100
本试剂盒用于检测补体成分3(C3),经检测与其它相似物质无明显交叉反应。
由于受到技术及样本来源的限制,不可能完成对所有相关或相似物质交叉反应检测,因此本试剂盒有可能与未经检测的其它物质有交叉反应。
分别于定值血清及血浆样本中加入一定量的补体成分3(C3)(加标样品),重复测定并计算其均值,回收率为测定值与理论值的比率。
样本 | 回收率范围(%) | 平均回收率(%) |
serum(n=5) | 78-92 | 88 |
EDTA plasma(n=5) | 87-102 | 92 |
heparin plasma(n=5) | 93-101 | 97 |
精密度用样品测定值的变异系数CV表示。CV(%) = SD/mean×100
批内差:取同批次试剂盒对低、中、高值定值样本进行定量检测,每份样本连续测定20 次,分别计算不同浓度样本的平均值及SD值。
批间差:选取3个不同批次的试剂盒分别对低、中、高值定值样本进行定量测定,每个样本使用同一试剂盒重复测定8次,分别计算不同浓度样本的平均值及SD值。
批内差: CV<10%
批间差: CV<12%
在定值血清及血浆样本内加入适量的补体成分3(C3),并倍比稀释成1:2,1:4,1:8,1:16的待测样本,线性范围即为稀释后样本中补体成分3(C3)含量的测定值与理论值的比率。
样本 | 1:2 | 1:4 | 1:8 | 1:16 |
serum(n=5) | 90-98% | 81-98% | 91-98% | 95-105% |
EDTA plasma(n=5) | 91-105% | 89-98% | 99-105% | 88-102% |
heparin plasma(n=5) | 79-93% | 89-96% | 89-96% | 78-92% |
经测定,试剂盒在有效期内按推荐温度保存,其活性降低率小于5%。
为减小外部因素对试剂盒破坏前后检测值的影响,实验室的环境条件需尽量保持一致,尤其是实验室内温度、湿度及温育条件。其次由同一实验员来进行操作可减少人为误差。
1. 实验前标准品、试剂及样本的准备;
2. 加样(标准品及样本)100µL,37°C孵育1小时;
3. 吸弃,加检测溶液A100µL,37°C孵育1小时;
4. 洗板3次;
5. 加检测溶液B100µL,37°C孵育30分钟;
6. 洗板5次;
7. 加TMB底物90µL,37°C孵育10-20分钟;
8. 加终止液50µL,立即450nm读数。
将补体成分3(C3)抗体包被于96孔微孔板中,制成固相载体,向微孔中分别加入标准品或标本,其中的补体成分3(C3)与连接于固相载体上的抗体结合,然后加入生物su化的补体成分3(C3)抗体,将未结合的生物su化抗体洗净后,加入HRP标记的亲和素,再次洗涤后加入TMB底物显色。TMB在过氧化物酶的催化下转化成蓝色,并在酸的作用下转化成Z终的黄色。颜色的深浅和样品中的补体成分3(C3)呈正相关。用酶标仪在450nm波长下测定吸光度(O.D.值),计算样品浓度。
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