尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)
Multiplex Assay Kit for Plasminogen Activator, Urokinase (uPA) ,etc. by FLIA (Flow Luminescence Immunoassay)
PLAU; ATF; URK; UK; UP-A; Abbokinase; Urokinase-Type Plasminogen Activator
(注:单次混测多因子不超过8个指标 )
- 编号LMA140Mu
- 物种Mus musculus (Mouse,小鼠) 相同的名称,不同的物种。
- 实验方法双抗夹心
- 反应时长3.5h
- 检测范围0.01-10ng/mL
- 灵敏度最小可检测剂量小于等于0.003 ng/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 8指标数 7指标数 6指标数 5指标数 4指标数 3指标数 2指标数1指标数
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特异性
本试剂盒用于检测尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法),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。
回收率
分别于定值血清及血浆样本中加入一定量的尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)(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) | 83-102 | 93 |
EDTA plasma(n=5) | 85-92 | 88 |
heparin plasma(n=5) | 78-102 | 97 |
精密度
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%
线性
在定值血清及血浆样本内加入适量的尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法),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尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)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) | 80-88% | 94-102% | 92-101% | 84-99% |
EDTA plasma(n=5) | 83-92% | 92-105% | 89-97% | 81-93% |
heparin plasma(n=5) | 91-98% | 80-93% | 81-102% | 92-105% |
稳定性
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。
实验流程
1. 实验前标准品、试剂及样本准备;
2. 加样(标准品、样本、磁珠)标准品或样本100μL及磁珠10μL,
37°C酶标板振荡器孵育90分钟;
3. 磁吸甩干,加检测溶液A100μL,37°C酶标板振荡器孵育60分钟;
4. 磁吸洗板3次;
5. 加检测溶液B100μL,37°C振动孵育30分钟;
6. 磁吸洗板3次;
7. 加鞘液100μL,旋涡震荡2分钟后读数。
实验原理
将尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)抗体包被于磁珠,制成固相载体,向微孔中分别加入标准品或标本以及磁珠,其中的尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)与连接于固相载体上的抗体结合,然后加入生物素化的尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)抗体,将未结合的生物素化抗体洗净后,加入PE标记的亲和素,再次彻底洗涤后即可上机读数。MFI值和样品中的尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法)呈正相关。
赠品
增值服务
相关产品
编号 | 适用物种:Mus musculus (Mouse,小鼠) | 应用(仅供研究使用,不用于临床诊断!) |
APA140Mu61 | 尿激酶型纤溶酶原激活因子(uPA)活性蛋白 | Cell culture; Activity Assays. |
RPA140Mu01 | 尿激酶型纤溶酶原激活因子(uPA)重组蛋白 | Positive Control; Immunogen; SDS-PAGE; WB. |
APA140Mu62 | 尿激酶型纤溶酶原激活因子(uPA)活性蛋白 | Cell culture; Activity Assays. |
RPA140Mu02 | 尿激酶型纤溶酶原激活因子(uPA)重组蛋白 | Positive Control; Immunogen; SDS-PAGE; WB. |
PAA140Mu01 | 尿激酶型纤溶酶原激活因子(uPA)多克隆抗体 | WB; IHC; ICC; IP. |
PAA140Mu02 | 尿激酶型纤溶酶原激活因子(uPA)多克隆抗体 | WB; IHC; ICC; IP. |
SEA140Mu | 尿激酶型纤溶酶原激活因子(uPA)检测试剂盒(酶联免疫吸附试验法) | Enzyme-linked immunosorbent assay for Antigen Detection. |
LMA140Mu | 尿激酶型纤溶酶原激活因子(uPA)等多因子检测试剂盒(流式荧光发光法) | FLIA Kit for Antigen Detection. |
参考文献
杂志 | 参考文献 |
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Oncotarget | Urokinase plasminogen activator secreted by cancer-associated fibroblasts induces tumor progression via PI3K/AKT and ERK signaling in esophageal squamous cell carcinoma [pubmed:28404945] |
Journal of allergy and clinical immunology | Cytokine and estrogen stimulation of endothelial cells augments activation of the prekallikrein-high molecular weight kininogen complex: Implications for hereditary angioedema. [pubmed:27826093] |
Molecular Medicine Reports | Effect of a synthetic inhibitor of urokinase plasminogen activator on the migration and invasion of human cervical cancer cells in vitro [Pubmed:29328476] |
Phytomedicine | Multi-omics analysis reveals the mechanisms of action and therapeutic regimens of traditional Chinese medicine, Bufei Jianpi granules: Implication for COPD drug … [Pubmed:35121390] |
Cellular and Molecular Life Sciences | IL4 stimulated macrophages promote axon regeneration after peripheral nerve injury by secreting uPA to stimulate uPAR upregulated in injured axons [Pubmed:35536429] |