產(chǎn)品名稱(chēng)： 人1,5-脫水葡萄糖醇/1,5-脫水山梨（1,5-AG）ELISA Kit
 
 英文名稱(chēng)： Human 1,5-anhydroglucitol （1,5-AG） ELISA kit
 
 貨號(hào)： CSB-E08988h
 
 規(guī)格： 96T
 
 種屬： Human
 
 待測(cè)物名稱(chēng)： 1,5-anhydroglucitol,1,5-AG
 
 縮寫(xiě)： 1,5AG
 
 樣本類(lèi)型： serum, plasma, tissue homogenates
 
 檢測(cè)范圍： 28.5 nmol/ml-500 nmol/ml
 
 靈敏度： 17.8 nmol/ml
 
 反應(yīng)時(shí)間： 1-5h
 
 所需樣本體積： 50-100ul
 
 檢測(cè)波長(zhǎng)： 450 nm
 
 用途： For research use only. Not for diagnostic use.
 
 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 Expert 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 IGF1 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.
  
相關(guān)產(chǎn)品：

 
產(chǎn)品名稱(chēng) 英文名稱(chēng) 貨號(hào) 規(guī)格
 人空泡毒素相關(guān)蛋白A（VacA）ELISA Kit  Human Vacuolating cytotoxin A（VacA）ELISA Kit  CSB-E08984h  96T 
        
 人玻連蛋白（VTN）ELISA Kit  Human vitronectin （VTN） ELISA Kit  CSB-E08983h  96T 
        
 人γ谷氨酸-半胱氨酸合成酶 （γ-GCS） ELISA Kit  Human γ glutamylcysteine synthetase （γ-GCS） ELISA Kit  CSB-E08980h  96T 
        
 人抗可溶性肝抗原抗體（SLA）ELISA Kit  Human anti-soluble liver antigen,SLA ELISA Kit  CSB-E08987h  96T 
        
 人波形蛋白（VIM）ELISA Kit  Human vimentin,VIM ELISA Kit  CSB-E08982h  96T 
        
 人超敏前列腺特異性抗原（PSA-U S）ELISA Kit  Human Ultra Sensitive Prostate Specific Antigen,PSA U S ELISA Kit  CSB-E08989h  96T 
        
 人膽囊收縮素/縮膽囊素八肽（CCK-8）ELISA Kit  Human cholecystokinin octapeptide,CCK-8 ELISA Kit  CSB-E08986h  96T