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當(dāng)前位置：廈門(mén)慧嘉生物科技有限公司>>ELISA試劑盒 >>小鼠的ELISA試劑盒 >>優(yōu)品質(zhì) 小鼠（OPGL）ELISA試劑盒 小鼠骨保護(hù)素配體（OPGL）ELISA試劑盒

優(yōu)品質(zhì) 小鼠（OPGL）ELISA試劑盒 小鼠骨保護(hù)素配體（OPGL）ELISA試劑盒

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廈門(mén)慧嘉生物公司*經(jīng)營(yíng)小鼠骨保護(hù)素配體(OPGL)ELISA試劑盒\(zhòng)Santa\Abcam\Cst\jackson \Pierce\Sigma\Amresco\Qiagen\Cayman\abnova\millipore\invitrogen\ merk \ ebioscience \prospec\peprotech細(xì)胞因子*

詳細(xì)介紹

 廈門(mén)慧嘉生物*專業(yè)銷售ELISA試劑盒\(zhòng)Santa \ Abcam \ Cst \ jackson \ Pierce \ Sigma \ Amresco \Qiagen \ Cayman \ abnova \ millipore \ invitrogen \ merk \ ebioscience \prospec \ peprotech細(xì)胞因子*。等生物試劑產(chǎn)品。實(shí)驗(yàn)為大，誠(chéng)信經(jīng)營(yíng)，為客戶提供“zui高質(zhì)量的產(chǎn)品”和“的服務(wù):  : 或登陸http://www.biohj.com（向客服人員索取原版說(shuō)明書(shū)）。歡迎廣大老師來(lái)詢！”

小鼠骨保護(hù)素配體（OPGL）ELISA試劑盒
小鼠乳鐵傳遞蛋白/乳鐵蛋白（LF/LTF）ELISA試劑盒
小鼠色素上皮衍生因子（PEDF）ELISA試劑盒
小鼠腎損傷分子1（Kim-1）ELISA試劑盒 
小鼠糖皮質(zhì)類固醇受體（GR）ELISA試劑盒
小鼠黃體生成素釋放激素（LHRH）ELISA試劑盒
小鼠α半乳糖基抗原（α-Gal）ELISA試劑盒 
小鼠β氨基己糖苷酶A（β-Hex A）ELISA試劑盒 
小鼠肺表面活性物質(zhì)相關(guān)蛋白A（SP-A）ELISA試劑盒
小鼠克拉拉細(xì)胞蛋白（CC16）ELISA試劑盒
小鼠β半乳糖苷酶（βGAL）ELISA試劑盒
小鼠腎上腺素（EPI）ELISA試劑盒
小鼠腎素（Renin）ELISA試劑盒
小鼠一氧化氮（NO）ELISA試劑盒
小鼠雌三醇（E3）ELISA試劑盒
小鼠雄烯二酮（ASD）ELISA試劑盒
小鼠游離睪酮（F-TESTO）ELISA試劑盒
小鼠睪酮（T）ELISA試劑盒
小鼠孕激素/孕酮（PROG）ELISA試劑盒 
小鼠可溶性核因子κB受體活化因子配基（sRANKL）ELISA試劑盒
小鼠降鈣素（CT）ELISA試劑盒
小鼠脫氫表雄酮硫酸酯（DHEA-S）ELISA試劑盒
小鼠內(nèi)皮素1（ET-1）ELISA試劑盒
小鼠雌二醇（E2）ELISA試劑盒
小鼠*（Cortisol）ELISA試劑盒
小鼠促甲狀腺素（TSH）ELISA試劑盒
小鼠兒茶酚胺（CA）ELISA試劑盒
小鼠白細(xì)胞介素-27（IL-27）ELISA試劑盒
小鼠白細(xì)胞介素-23（IL-23）ELISA試劑盒

檢測(cè)范圍：

Request Information

靈敏度：

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反應(yīng)時(shí)間：

1-3h

所需樣本體積：

50-100ul

檢測(cè)波長(zhǎng)：

450 nm

說(shuō)明書(shū)：

（向客服人員索取原版說(shuō)明書(shū)）

原理 ：

This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for ACHE has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any ACHE present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for ACHE is added to the wells. After washing, avidin conjugated Horseradish Peroxidase （HRP） is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of ACHE bound in the initial step. The color development is stopped and the intensity of the color is measured.

特異性：

This assay has high sensitivity and excellent specificity for detection of Rat ACHE. No significant cross-reactivity or interference between Rat ACHE and analogues was observed.

精密度：

Intra-assay Precision （Precision within an assay）: CV%<8%
Three samples of known concentration were tested twenty times on one plate to assess.
Inter-assay Precision （Precision between assays）: CV%<10%
Three samples of known concentration were tested in twenty assays to assess.

樣本搜集及儲(chǔ)存：

Serum: Use a serum separator tube （SST） and allow samples to clot for two hours at room temperature or overnight at 4°C before centrifugation for 15 minutes at 1000 ×g. Remove serum and assay immediay or aliquot and store samples at -20°C or -80°C. Avoid repeated freeze-thaw cycles.
Plasma: Collect plasma using EDTA, or heparin as an anticoagulant. Centrifuge for 15 minutes at 1000 ×g at 2-8°C within 30 minutes of collection. Assay immediay or aliquot and store samples at -20°C or -80°C. Avoid repeated freeze-thaw cycles.

檢測(cè)步驟：

Bring all reagents and samples to room temperature before use. Centrifuge the sample again after thawing before the assay. It is recommended that all samples and standards be assayed in duplicate.
1. Prepare all reagents, working standards, and samples as directed in the previous sections.
2. Refer to the Assay Layout Sheet to determine the number of wells to be used and put any remaining wells and the desiccant back into the pouch and seal the ziploc, store unused wells at 4°C.
3. Add 100μl of standard and sample per well. Cover with the adhesive strip provided. Incubate for 2 hours at 37°C. A plate layout is provided to record standards and samples assayed.
4. Remove the liquid of each well, don't wash.
5. Add 100μl of Biotin-antibody （1x） to each well. Cover with a new adhesive strip. Incubate for 1 hour at 37°C. （Biotin-antibody （1x） may appear cloudy. Warm up to room temperature and mix gently until solution appears uniform.）
6. Aspirate each well and wash, repeating the process two times for a total of three washes. Wash by filling each well with Wash Buffer （200μl） using a squirt bottle, multi-channel pipette, manifold dispenser, or autowasher, and let it stand for 2 minutes, complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining wash Buffer by aspirating ordecanting. Invert the plate and blot it against clean paper towels.
7. Add 100μl of HRP-avidin （1x） to each well. Cover the microtiter plate with a new adhesive strip. Incubate for 1 hour at 37°C.
8. Repeat the aspiration/wash process for five times as in step 6.
9. Add 90μl of TMB Substrate to each well. Incubate for 15-30 minutes at 37°C. Protect from light.
10. Add 50μl of Stop Solution to each well, gently tap the plate to ensure thorough mixing.
11. Determine the optical density of each well within 5 minutes, using a microplate reader set to 450 nm. If wavelength correction is available, set to 540 nm or 570 nm. Subtract readings at 540 nm or 570 nm from the readings at 450 nm. This subtraction will correct for optical imperfections in the plate. Readings made directly at 450 nm without correction may be higher and less accurate.

結(jié)果計(jì)算：

Using the professional soft "Curve Exert 1.3" to make a standard curve is recommended, which can be downloaded from our web.
Average the duplicate readings for each standard and sample and subtract the average zero standard optical density.
Create a standard curve by reducing the data using computer software capable of generating a four parameter logistic （4-PL） curve-fit. As an alternative, construct a standard curve by plotting the mean absorbance for each standard on the x-axis against the concentration on the y-axis and draw a best fit curve through the points on the graph. The data may be linearized by plotting the log of the ACHE concentrations versus the log of the O.D. and the best fit line can be determined by regression analysis. This procedure will produce an adequate but less precise fit of the data.
If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.

 

廈門(mén)慧嘉生物*專業(yè)銷售ELISA試劑盒\(zhòng)Santa \ Abcam \ Cst \ jackson \ Pierce \ Sigma \ Amresco \Qiagen \ Cayman \ abnova \ millipore \ invitrogen \ merk \ ebioscience \prospec \ peprotech細(xì)胞因子*。等生物試劑產(chǎn)品。實(shí)驗(yàn)為大，誠(chéng)信經(jīng)營(yíng)，為客戶提供“zui高質(zhì)量的產(chǎn)品”和“的服務(wù)”:  : 或登陸http://www.biohj.com（向客服人員索取原版說(shuō)明書(shū)）。歡迎廣大老師來(lái)詢！


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