細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)
Multiplex Assay Kit for Cytochrome C Oxidase Subunit II (COX2) ,etc. by FLIA (Flow Luminescence Immunoassay)
MTCO2; MT-CO2; COII; COXII; Mitochondrially Encoded Cytochrome C Oxidase II; Cytochrome c oxidase polypeptide II
(注:單次混測多因子不超過8個指標 )
- 編號ULMD284Mu
- 物種Mus musculus (Mouse,小鼠) 相同的名稱,不同的物種。
- 實驗方法雙抗夾心
- 反應時長3.5h
- 檢測范圍0.02-20ng/mL
- 靈敏度最小可檢測劑量小于等于0.007 ng/mL.
- 樣本類型Tissue homogenates, cell lysates and other biological fluids
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特異性
                        本試劑盒用于檢測細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法),經檢測與其它相似物質無明顯交叉反應。
                        由于受到技術及樣本來源的限制,不可能完成對所有相關或相似物質交叉反應檢測,因此本試劑盒有可能與未經檢測的其它物質有交叉反應。
                    
回收率
分別于定值血清及血漿樣本中加入一定量的細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)(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) | 96-104 | 101 | 
| EDTA plasma(n=5) | 78-103 | 99 | 
| heparin plasma(n=5) | 98-105 | 102 | 
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細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)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細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)含量的測定值與理論值的比率。
| 樣本 | 1:2 | 1:4 | 1:8 | 1:16 | 
| serum(n=5) | 95-104% | 85-94% | 92-99% | 80-104% | 
| EDTA plasma(n=5) | 92-105% | 81-91% | 87-95% | 82-97% | 
| heparin plasma(n=5) | 93-105% | 98-105% | 88-98% | 90-97% | 
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. 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,
                                37°C酶標板振蕩器孵育90分鐘;
                            3. 磁吸甩干,加檢測溶液A100μL,37°C酶標板振蕩器孵育60分鐘;
                            4. 磁吸洗板3次;
                            5. 加檢測溶液B100μL,37°C振動孵育30分鐘;
                            6. 磁吸洗板3次;
                            7. 加鞘液100μL,旋渦震蕩2分鐘后讀數。
                
實驗原理
將細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)抗體包被于磁珠,制成固相載體,向微孔中分別加入標準品或標本以及磁珠,其中的細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)與連接于固相載體上的抗體結合,然后加入生物素化的細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)抗體,將未結合的生物素化抗體洗凈后,加入PE標記的親和素,再次徹底洗滌后即可上機讀數。MFI值和樣品中的細胞色素C氧化酶亞基Ⅱ(COX2)等多因子檢測試劑盒(流式熒光發(fā)光法)呈正相關。
贈品
增值服務
相關產品
| 編號 | 適用物種:Mus musculus (Mouse,小鼠) | 應用(僅供研究使用,不用于臨床診斷!) | 
| USED284Mu | 細胞色素C氧化酶亞基Ⅱ(COX2)檢測試劑盒(酶聯免疫吸附試驗法) | Enzyme-linked immunosorbent assay for Antigen Detection. | 
| ULMD284Mu | 細胞色素C氧化酶亞基Ⅱ(COX2)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
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