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小鼠凝血因子Ⅱ(FⅡ)ELISA試劑盒

點(diǎn)擊次數(shù):14發(fā)布時(shí)間:2016/6/7 20:45:09

小鼠凝血因子Ⅱ(FⅡ)ELISA試劑盒

更新日期:2016/6/7 20:45:09

所 在 地:中國(guó)大陸

產(chǎn)品型號(hào):

簡(jiǎn)單介紹:小鼠凝血因子Ⅱ(FⅡ)ELISA試劑盒 貨號(hào)QY-M30381 國(guó)產(chǎn)/進(jìn)口原裝 48T/96T 美洲 品牌QYBIO elisa酶聯(lián)免疫分析法 詳細(xì)請(qǐng)見說明書

相關(guān)標(biāo)簽:小鼠凝血因子Ⅱ(FⅡ)ELISA試劑盒 

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詳細(xì)內(nèi)容

 小鼠凝血因子Ⅱ(F)ELISA試劑盒齊一生物銷售:0216034 8496;181214 53965;173021 04490

規(guī)格:小規(guī)格48T.大規(guī)格96T

樣本標(biāo)準(zhǔn):血清,血漿,尿液,胸腹水,腦脊液,細(xì)胞培養(yǎng)上清,組織勻漿等

檢測(cè)方法:酶聯(lián)免疫分析(ELISA

運(yùn)輸保存:2~8°貯存.保質(zhì)期:6個(gè)月

試驗(yàn)所需自備物品:

1. 酶標(biāo)儀(450nm 波長(zhǎng)濾光片)

2. 高精度移液器,EP 管及一次性吸頭

3. 37℃恒溫箱,雙蒸水或去離子水

4. 吸水紙

 

小鼠凝血因子Ⅱ(F)ELISA試劑盒齊一生物主要經(jīng)營(yíng)進(jìn)口原裝Elisa試劑盒,檢測(cè)試劑種類齊全,價(jià)格實(shí)惠!購買齊一生物產(chǎn)品的新老客戶都可享免費(fèi)代測(cè)實(shí)驗(yàn)服務(wù),全程提供技術(shù)支持.如需其它Elisa試劑盒說明書及產(chǎn)品價(jià)格,可來電咨詢齊一生物銷售:021-6034 8496181214 53965173021 04490

 

試劑盒特點(diǎn)

一、高效、靈敏、特異的抗體;

二、穩(wěn)定的重復(fù)性和可靠性;

三、吸附性能好,空白值低,孔底透明度高的固相載體;

四、適用血清、血漿、組織勻漿液、細(xì)胞培養(yǎng)上清液、尿液等等多種標(biāo)本類型;

 

試劑盒可概括四個(gè)方面:

1、免疫酶染色各種細(xì)胞內(nèi)成份的定位.

2、研究抗酶抗體的合成.

3、顯現(xiàn)微量的免疫沉淀反應(yīng).

4、定量檢測(cè)體液中抗原或抗體成份.

小鼠凝血因子Ⅱ(F)ELISA試劑盒ELISA試劑盒為您節(jié)省實(shí)驗(yàn)經(jīng)費(fèi).

elisa試劑盒回收率是反應(yīng)待測(cè)物在樣品分析過程中的損失的程度,損失越少,回收率越高,如果作標(biāo)液1PPM,就是1毫克/,而作出標(biāo)準(zhǔn)數(shù)據(jù)為0.99毫克/,就是說你的回收率是99%,這個(gè)與真實(shí)成分有密切的關(guān)系,說明方法的準(zhǔn)確度.比如水中總無機(jī)氯含量測(cè)定,樣品水中含有無機(jī)氯20mg/L,100mL被測(cè)水樣品,加入0.1mL濃度為10mg/mL的含無機(jī)氯標(biāo)準(zhǔn)樣品,測(cè)定時(shí)忽略體積變化,如果測(cè)定出樣品中無機(jī)氯為2.98mg/L,則認(rèn)為回收率為99%.

小鼠凝血因子Ⅱ(F)ELISA試劑盒試劑盒制備方法包括以下步驟:

1)抗原表位的計(jì)算機(jī)篩選;

2)抗原的制備;

3)血清的采集;

4)間接ELISA方法的建立;

5)間接ELISA方法的敏感性和特異性驗(yàn)證;

6)試劑盒的穩(wěn)定性驗(yàn)證;

7)對(duì)大量樣本進(jìn)行檢測(cè).該方法簡(jiǎn)單、快速、靈敏度高、特異性強(qiáng)、穩(wěn)定性合格、重復(fù)性好.應(yīng)用本發(fā)明制得的試劑盒能有效檢出樣本含量.適用于大批量樣本的檢測(cè)

試劑盒安全性提示:

1.工作人員實(shí)驗(yàn)中避免直接接觸終止液和底物A、B。一旦接觸到這些液體,請(qǐng)盡快用水沖洗。

2.實(shí)驗(yàn)中不要吃喝、抽煙或使用化妝品。

3.不要用嘴吸取試劑盒里的任何成份。

小鼠凝血因子Ⅱ(F)ELISA試劑盒齊一生物【友情提示】:本產(chǎn)品僅供科研研究使用,不得用于人體臨床直接檢測(cè)。避免給您帶來不必要的損失,請(qǐng)仔細(xì)閱讀購買說明!

 

���R ��(j���ng=EN-US>1-2分鐘,350μl/每孔,甩干。
6.        
依序每孔加底物溶液90μl,37℃避光顯色(30分鐘內(nèi),此時(shí)肉眼可見標(biāo)準(zhǔn)品的前3-4孔有明顯的梯度藍(lán)色,后3-4孔梯度不明顯,即可終止)。
7.        
依序每孔加終止溶液50μl,終止反應(yīng)(此時(shí)藍(lán)色立轉(zhuǎn)黃色)。終止液的加入順序應(yīng)盡量與底物液的加入順序相同。為了保證實(shí)驗(yàn)結(jié)果的準(zhǔn)確性,底物反應(yīng)時(shí)間到后應(yīng)盡快加入終止液。
8.        
用酶聯(lián)儀在450nm波長(zhǎng)依序測(cè)量各孔的光密度(OD值)。 在加終止液后15分鐘以內(nèi)進(jìn)行檢測(cè)。
小鼠的牛血清白蛋白殘留檢測(cè)ELISA試劑盒注:
1.
用戶在初次使用試劑盒時(shí),應(yīng)將各種試劑管離心數(shù)分鐘,以便試劑集中到管底。
2.
每次實(shí)驗(yàn)留一孔作為空白調(diào)零孔,該孔不加任何試劑,只是*后加底物溶液及2N H2SO4。測(cè)量時(shí)先用此孔調(diào)OD值至零。
3.
為防止樣品蒸發(fā),試驗(yàn)時(shí)將反應(yīng)板放于鋪有濕布的密閉盒內(nèi),酶標(biāo)板加上蓋或覆膜。
4.
未使用完的酶標(biāo)板或者試劑,請(qǐng)于2-8℃保存。標(biāo)準(zhǔn)品、生物素標(biāo)記抗體工作液、辣根過氧化物酶標(biāo)記親和素工作液請(qǐng)依據(jù)所需的量配置使用。請(qǐng)勿重復(fù)使用已稀釋過的標(biāo)準(zhǔn)品、生物素標(biāo)記抗體工作液或、辣根過氧化物酶標(biāo)記親和素工作液。
5.
建議檢測(cè)樣品時(shí)均設(shè)雙孔測(cè)定,以保證檢測(cè)結(jié)果的準(zhǔn)確性。
以上資料僅供您參考,如有問題歡迎來電,齊一生物銷售:0216034 8496;181214 53965;173021 04490

 

 

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Data Analysis – The Comprehensive Validation Support plan encompasses data collection (quants, amps, CE) during the on-site visit. The laboratory may be responsible for sharing (typically electronically via e-mail) any validation data requested after the on-site visit. A QIAGEN specialist will complete all of the data analysis produced from the validation study design. This includes qPCR (quant) and STR (amp) analysis and linkage to starting samples.


Validation data CD/flashdrive – QIAGEN will review the validation data and draft a validation summary document, ensuring compliance with the FBI's QAS requirements/standards. QIAGEN will send validation data in an electronic format (email/CD/flashdrive) to the laboratory. The laboratory is responsible for final compilation, any format change preferences, review and signoff of the validation report. The documentation provided by QIAGEN will aide in demonstrating compliance with all accreditation guidelines during laboratory audits. Should a hard copy of the validation study be preferred, the laboratory is required to specify prior to the onset of the validation.


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