北京Elisa试剂盒 价格,人沙眼衣原体(CT)ELISA Kit 说明书

 北京elisa试剂盒 价格,人沙眼衣原体（CT）ELISA Kit  说明书

产品名称： 人沙眼衣原体抗原（CT）ELISA kit
 
 英文名称： Human chlamydia trachomatis,CT ELISA kit
 
 规格： 96T
 
 种属： Human
 
 待测物名称： chlamydia trachomatis （CT）
 
 缩写： CT
 
 反应时间： 1-5h
 
 所需样本体积： 50-100ul
 
 检测波长： 450nm
 
 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.
 
 样本搜集及储存： 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 immediately 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 immediately or aliquot ａnd store samples at -20°C or -80°C. Avoid repeated freeze-thaw cycles.
 
 检测步骤： 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.
 
 结果计算： 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 CT 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.
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