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微管蛋白β(TUBb)等多因子檢測試劑盒(流式熒光發(fā)光法)

Multiplex Assay Kit for Tubulin Beta (TUBb) ,etc. by FLIA (Flow Luminescence Immunoassay)

TUB-B; TUBB5; TUBB1; M40

(注:單次混測多因子不超過8個指標 )

  • 微管蛋白β(TUBb)等多因子檢測試劑盒(流式熒光發(fā)光法)產品包裝(模擬)
  • 微管蛋白β(TUBb)等多因子檢測試劑盒(流式熒光發(fā)光法)產品包裝(模擬)
  • Certificate通過ISO 9001、ISO 13485質量體系認證

特異性

本試劑盒對檢測微管蛋白β(TUBb)具有較高的靈敏度。
經檢測人、小鼠、大鼠之間有100%的交叉反映。

回收率

分別于定值血清及血漿樣本中加入一定量的微管蛋白β(TUBb)(加標樣品),重復測定并計算其均值,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)97-104101
EDTA plasma(n=5)88-9793
heparin plasma(n=5)88-10293

精密度

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

線性

在定值血清及血漿樣本內加入適量的微管蛋白β(TUBb),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微管蛋白β(TUBb)含量的測定值與理論值的比率。

樣本1:21:41:81:16
serum(n=5)94-105%78-98%84-93%86-104%
EDTA plasma(n=5)97-105%91-99%78-91%92-105%
heparin plasma(n=5)88-95%88-105%91-101%89-96%

穩(wěn)定性

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

實驗流程

1、向實驗板每孔內加入200μL分析緩沖液以預濕;
2、實驗前標準品、試劑及樣本準備;
2、加樣(標準品、樣本、磁珠),標準品或樣本100μL及磁珠10μL,25°C酶標板振蕩器孵育2小時;
3、磁吸甩干,加檢測溶液A 100μL,25°C酶標板振蕩器孵育1小時;
4、磁吸甩干,加檢測溶液B 100μL,25°C振動孵育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。

實驗原理

將微管蛋白β(TUBb)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準品或標本以及磁珠,其中的微管蛋白β(TUBb)與連接于固相載體上的抗體結合,然后加入生物素化的微管蛋白β(TUBb)抗體,加入PE標記的親和素,上機讀數。MFI值和樣品中的微管蛋白β(TUBb)濃度呈正相關。

贈品

相關產品

編號適用物種:Homo sapiens (Human,人), Mus musculus (Mouse,小鼠), Rattus norvegicus (Rat,大鼠)應用(僅供研究使用,不用于臨床診斷!)
CAB870Mi01抗微管蛋白β(TUBb)多克隆抗體WB
CAB870Mi22抗微管蛋白β(TUBb)單克隆抗體WB; IHC; ICC/IF
SEB870Mi微管蛋白β(TUBb)檢測試劑盒(酶聯免疫吸附試驗法)Enzyme-linked immunosorbent assay for Antigen Detection.
LMB870Mi微管蛋白β(TUBb)等多因子檢測試劑盒(流式熒光發(fā)光法)FLIA Kit for Antigen Detection.

參考文獻

雜志參考文獻
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