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腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)

Multiplex Assay Kit for Renalase (RNLS) ,etc. by CBA (Cytometric Bead Array)

MAO-C; C10orf59; FAD-Dependent Amine Oxidase; Monoamine oxidase-C; alpha-NAD(P)H oxidase/anomerase

  • 腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)產(chǎn)品包裝(模擬)
  • 腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)產(chǎn)品包裝(模擬)
  • Certificate通過ISO 9001、ISO 13485質(zhì)量體系認(rèn)證

特異性

本試劑盒用于檢測腎酶(RNLS)等多因子檢測試劑盒(流式熒光法),經(jīng)檢測與其它相似物質(zhì)無明顯交叉反應(yīng)。
由于受到技術(shù)及樣本來源的限制,不可能完成對(duì)所有相關(guān)或相似物質(zhì)交叉反應(yīng)檢測,因此本試劑盒有可能與未經(jīng)檢測的其它物質(zhì)有交叉反應(yīng)。

回收率

分別于定值血清及血漿樣本中加入一定量的腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)(加標(biāo)樣品),重復(fù)測定并計(jì)算其均值,回收率為測定值與理論值的比率。

樣本回收率范圍(%)平均回收率(%)
serum(n=5)98-105102
EDTA plasma(n=5)90-10198
heparin plasma(n=5)80-10182

精密度

精密度用樣品測定值的變異系數(shù)CV表示。CV(%) = SD/mean×100
批內(nèi)差:取同批次試劑盒對(duì)低、中、高值定值樣本進(jìn)行定量檢測,每份樣本連續(xù)測定20 次,分別計(jì)算不同濃度樣本的平均值及SD值。
批間差:選取3個(gè)不同批次的試劑盒分別對(duì)低、中、高值定值樣本進(jìn)行定量測定,每個(gè)樣本使用同一試劑盒重復(fù)測定8次,分別計(jì)算不同濃度樣本的平均值及SD值。
批內(nèi)差: CV<10%
批間差: CV<12%

線性

在定值血清及血漿樣本內(nèi)加入適量的腎酶(RNLS)等多因子檢測試劑盒(流式熒光法),并倍比稀釋成1:2,1:4,1:8,1:16的待測樣本,線性范圍即為稀釋后樣本中腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)含量的測定值與理論值的比率。

樣本1:21:41:81:16
serum(n=5)82-95%96-103%90-97%82-99%
EDTA plasma(n=5)80-90%92-99%96-104%90-99%
heparin plasma(n=5)78-101%80-97%79-99%91-98%

穩(wěn)定性

經(jīng)測定,試劑盒在有效期內(nèi)按推薦溫度保存,其活性降低率小于5%。
為減小外部因素對(duì)試劑盒破壞前后檢測值的影響,實(shí)驗(yàn)室的環(huán)境條件需盡量保持一致,尤其是實(shí)驗(yàn)室內(nèi)溫度、濕度及溫育條件。其次由同一實(shí)驗(yàn)員來進(jìn)行操作可減少人為誤差。

實(shí)驗(yàn)流程

1、向?qū)嶒?yàn)板每孔內(nèi)加入200μL分析緩沖液以預(yù)濕;
2、實(shí)驗(yàn)前標(biāo)準(zhǔn)品、試劑及樣本準(zhǔn)備;
3、加樣(標(biāo)準(zhǔn)品、樣本、磁珠),標(biāo)準(zhǔn)品或樣本100μL及磁珠10μL,25°C酶標(biāo)板振蕩器孵育2小時(shí);
4、磁吸甩干,加檢測溶液A 100μL,25°C酶標(biāo)板振蕩器孵育1小時(shí);
5、磁吸甩干,加檢測溶液B 100μL,25°C振動(dòng)孵育30分鐘;
6、磁吸洗板1次;
7、加鞘液100μL,旋渦震蕩10分鐘后讀數(shù)。

實(shí)驗(yàn)原理

將腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)抗體包被于磁性微球表面,制成固相載體,向微孔中分別加入標(biāo)準(zhǔn)品或標(biāo)本以及磁珠,其中的腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)與連接于固相載體上的抗體結(jié)合,然后加入生物素化的腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)抗體,加入PE標(biāo)記的親和素,用流式細(xì)胞儀讀數(shù)。MFI值和樣品中的腎酶(RNLS)等多因子檢測試劑盒(流式熒光法)濃度呈正相關(guān)。

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參考文獻(xiàn)

雜志參考文獻(xiàn)
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