氨基端前腦鈉素(NT-ProBNP)檢測試劑盒(酶聯(lián)免疫吸附試驗法)
ELISA Kit for N-Terminal Pro-Brain Natriuretic Peptide (NT-ProBNP)
NT-Pro-BNP; ; N-BNP
- 編號CEA485Rb
 - 物種Oryctolagus cuniculus (Rabbit,兔)相同的名稱,不同的物種。
 - 實驗方法競爭抑制
 - 反應(yīng)時長2h
 - 檢測范圍61.7-5,000pg/mL
 - 靈敏度最小可檢測劑量小于等于24.5pg/mL.
 - 樣本類型serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
 - 下載英文說明書 中文說明書
 - 規(guī)格48T96T96T*596T*1096T*100
 - 價格¥ 2730¥ 3900¥ 17550¥ 33150¥ 273000
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特異性
                        本試劑盒用于檢測氨基端前腦鈉素(NT-ProBNP),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氨基端前腦鈉素(NT-ProBNP)(加標樣品),重復(fù)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) | 86-93 | 89 | 
| EDTA plasma(n=5) | 98-105 | 102 | 
| heparin plasma(n=5) | 80-97 | 92 | 
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(fù)測定8次,分別計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)加入適量的氨基端前腦鈉素(NT-ProBNP),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氨基端前腦鈉素(NT-ProBNP)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) | 89-102% | 79-103% | 85-102% | 98-105% | 
| EDTA plasma(n=5) | 84-94% | 91-99% | 80-102% | 99-105% | 
| heparin plasma(n=5) | 87-98% | 79-94% | 91-99% | 86-101% | 
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(nèi)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、試劑及樣本的準備;
                            2. 加樣(標準品及樣本)50µL,
                                加入50µL檢測液A(臨用前配制);
                                37°C溫育1小時。
                            3. 洗板3次;
                            4. 加檢測溶液B100µL,37°C孵育30分鐘;
                            5. 洗板5次;
                            6. 加TMB底物90µL,37°C孵育10-20分鐘;
                            7. 加終止液50µL,立即450nm讀數(shù)。
實驗原理
本試劑盒應(yīng)用競爭抑制酶聯(lián)免疫分析法測定標本中待測物質(zhì)水平。將氨基端前腦鈉素(NT-ProBNP)單克隆抗體包被微孔板,制成固相載體,往包被抗體的微孔中同時加入生物素標記的抗原和待測抗原(標準品或樣本),待測抗原與生物素標記抗原對特異性抗體進行競爭結(jié)合。溫育后經(jīng)洗滌去掉未結(jié)合物,然后加入HRP標記的親和素,經(jīng)過溫育和徹底洗滌后加入底物TMB顯色。TMB在過氧化物酶的催化下轉(zhuǎn)化成藍色,并在酸的作用下轉(zhuǎn)化成最終的黃色。待測標本濃度越高,標記抗原和抗體的結(jié)合就越受到抑制,顯色愈淺。顯色的深淺與酶量呈正相關(guān),而與樣品中待測物質(zhì)含量呈負相關(guān)。用酶標儀在450nm波長下測定吸光度(O.D.值),計算樣品濃度。
相關(guān)產(chǎn)品
| 編號 | 適用物種:Oryctolagus cuniculus (Rabbit,兔) | 應(yīng)用(僅供研究使用,不用于臨床診斷!) | 
| SEA485Rb | 氨基端前腦鈉素(NT-ProBNP)檢測試劑盒(酶聯(lián)免疫吸附試驗法) | Enzyme-linked immunosorbent assay for Antigen Detection. | 
| CEA485Rb | 氨基端前腦鈉素(NT-ProBNP)檢測試劑盒(酶聯(lián)免疫吸附試驗法) | Enzyme-linked immunosorbent assay for Antigen Detection. | 
| LMA485Rb | 氨基端前腦鈉素(NT-ProBNP)等多因子檢測試劑盒(流式熒光發(fā)光法) | FLIA Kit for Antigen Detection. | 
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