凋亡相关因子(FAS)等多因子检测试剂盒(流式荧光发光法)

Multiplex Assay Kit for Factor Related Apoptosis (FAS) ,etc. by FLIA (Flow Luminescence Immunoassay)

CD95; ALPS1A; ALPS1-A; APO1; APT1; FAS1; FASTM; TNFRSF6; Fas Receptor; TNF Receptor Superfamily Member 6; Tumor Necrosis Factor Receptor Superfamily Member 6

(注:单次混测多因子不超过8个指标 )

  • 凋亡相关因子(FAS)等多因子检测试剂盒(流式荧光发光法)产品包装(模拟)
  • 凋亡相关因子(FAS)等多因子检测试剂盒(流式荧光发光法)产品包装(模拟)
  • Certificate通过ISO 9001、ISO 13485质量体系认证

特异性

本试剂盒用于检测凋亡相关因子(FAS)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凋亡相关因子(FAS)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)79-9182
EDTA plasma(n=5)80-9484
heparin plasma(n=5)87-9491
sodium citrate plasma(n=5)98-105102

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凋亡相关因子(FAS)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凋亡相关因子(FAS)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1:21:41:81:16
serum(n=5)83-91%93-101%88-95%89-98%
EDTA plasma(n=5)80-102%80-94%79-89%90-99%
heparin plasma(n=5)83-94%78-92%96-104%79-103%
sodium citrate plasma(n=5)86-102%95-103%83-97%81-97%

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

将凋亡相关因子(FAS)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,其中的凋亡相关因子(FAS)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凋亡相关因子(FAS)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值和样品中的凋亡相关因子(FAS)等多因子检测试剂盒(流式荧光发光法)呈正相关。

赠品

相关产品

编号适用物种:Rattus norvegicus (Rat,大鼠)应用(仅供研究使用,不用于临床诊断!)
EPA030Ra62凋亡相关因子(FAS)真核蛋白Positive Control; Immunogen; SDS-PAGE; WB.
EPA030Ra61凋亡相关因子(FAS)真核蛋白Positive Control; Immunogen; SDS-PAGE; WB.
RPA030Ra03凋亡相关因子(FAS)重组蛋白Positive Control; Immunogen; SDS-PAGE; WB.
RPA030Ra01凋亡相关因子(FAS)重组蛋白Positive Control; Immunogen; SDS-PAGE; WB.
RPA030Ra02凋亡相关因子(FAS)重组蛋白Positive Control; Immunogen; SDS-PAGE; WB.
APA030Ra61凋亡相关因子(FAS)活性蛋白Cell culture; Activity Assays.
PAA030Ra02凋亡相关因子(FAS)多克隆抗体WB; IHC; ICC; IP.
PAA030Ra06凋亡相关因子(FAS)多克隆抗体WB; IHC; ICC; IP.
PAA030Ra03凋亡相关因子(FAS)多克隆抗体WB; IHC; ICC; IP.
PAA030Ra01凋亡相关因子(FAS)多克隆抗体WB; IHC; ICC; IP.
LAA030Ra81凋亡相关因子(FAS)多克隆抗体(异硫氰酸荧光素标记)WB; IHC; ICC; IF.
LAA030Ra71凋亡相关因子(FAS)多克隆抗体(生物素标记)WB; IHC; ICC.
MAA030Ra21凋亡相关因子(FAS)单克隆抗体WB; IHC; ICC; IP.
SEA030Ra凋亡相关因子(FAS)检测试剂盒(酶联免疫吸附试验法)Enzyme-linked immunosorbent assay for Antigen Detection.
LMA030Ra凋亡相关因子(FAS)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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Scientific ReportsEGF-mediated reduced miR-92a-1-5p controls HTR-8/SVneo cell invasion through activation of MAPK8 and FAS which in turn increase MMP-2/-9 expression[Pubmed: 32703964]