欧美……一区二区三区,欧美日韩亚洲另类视频,亚洲国产欧美日韩中字,日本一区二区三区dvd视频在线

產(chǎn)品推薦:氣相|液相|光譜|質(zhì)譜|電化學(xué)|元素分析|水分測(cè)定儀|樣品前處理|試驗(yàn)機(jī)|培養(yǎng)箱


化工儀器網(wǎng)>技術(shù)中心>儀器文獻(xiàn)>正文

歡迎聯(lián)系我

有什么可以幫您? 在線咨詢

Human MMP26 elisakit說(shuō)明書

來(lái)源:上海武昊經(jīng)貿(mào)有限公司   2012年06月08日 16:06  

Human  Matrix Metalloproteinase 26,MMP26 ELISA Kit;Human MMP26 elisakit 說(shuō)明書

 
FOR IN VITRO USE AND RESEARCH USE ONLY
NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES
 
[ INTENDED USE ]
 quantitative measurement of MMP26 in human serum,plasma.
 
[ TEST PRINCIPLE ]
The microtiter plate provided in this kit has been pre-coated with an antibody specific to MMP26. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for MMP26. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain MMP26, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of MMP26 in the samples is then determined by comparing
the O.D. of the samples to the standard curve.
 
[ ASSAY PROCEDURE ]
1. Determine wells for diluted standard, blank and sample. Prepare 7 wells for standard, 1 well for blank.Add 100μL each of dilutions of standard (read Reagent Preparation), blank and samples into the appropriate wells. Cover with the Plate sealer. Incubate for 2 hours at 37oC.
2. Remove the liquid of each well, don’t wash.
3. Add 100μL of Detection Reagent A working solution to each well. Incubate for 1 hour at 37oC after covering it with the Plate sealer.
4. Aspirate the solution and wash with 350μL of 1× Wash Solution to each well using a squirt bottle,
multi-channel pipette, manifold dispenser or autowasher, and let it sit for 1~2 minutes. Remove the remaining liquid from all wells compley by snapping the plate onto absorbent paper. Totally wash 3 times. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against absorbent paper.
5. Add 100μL of Detection Reagent B working solution to each well. Incubate for 30 minutes at 37oC after covering it with the Plate sealer.
6. Repeat the aspiration/wash process for total 5 times as conducted in step 4.
7. Add 90μL of Substrate Solution to each well. Cover with a new Plate sealer. Incubate for 15 - 25 minutes at 37oC (Don't exceed 30 minutes). Protect from light. The liquid will turn blue by the addition of Substrate Solution.
8. Add 50μL of Stop Solution to each well. The liquid will turn yellow by the addition of Stop solution. Mix the liquid by tapping the side of the plate. If color change does not appear uniform, gently tap the plate to ensure thorough mixing.
9. Remove any drop of water and fingerprint on the bottom of the plate and confirm there is no bubble on the surface of the liquid. Then, run the microplate reader and conduct measurement at 450nm immediay.
 
[ TYPICAL DATA ]
In order to make the calculation easier, we plot the O.D. value of the standard (X-axis) against the known concentration of the standard (Y-axis), although concentration is the independent variable and O.D. value is the dependent variable. However, the O.D. values of the standard curve may vary according to the conditions of assay performance (e.g. operator, pipetting technique, washing technique or temperature effects), plotting log of the data to establish standard curve for each test is recommended. Typical standard curve below is provided for reference only.
Typical Standard Curve for Human MMP26 ELISA.
 
[ DETECTION RANGE ]
0.156-10ng/mL. The standard curve concentrations used for the ELISA’s were 10ng/mL, 5ng/mL, 2.5ng/mL,1.25ng/mL, 0.625ng/mL, 0.312ng/mL, 0.156ng/mL.
 
[ SENSITIVITY ]
The minimum detectable dose of human MMP26 is typically less than 0.052ng/mL.
The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined by adding two standard deviations to the mean optical density value of twenty zero standard replicates and calculating the corresponding concentration.
 
 
[ ASSAY PROCEDURE SUMMARY ]
1. Prepare all reagents, samples and standards;
2. Add 100μL standard or sample to each well. Incubate 2 hours at 37oC;
3. Add 100μL prepared Detection Reagent A. Incubate 1 hour at 37oC;
4. Aspirate and wash 3 times;
5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37oC;
6. Aspirate and wash 5 times;
7. Add 90μL Substrate Solution. Incubate 15-25 minutes at 37oC;
8. Add 50μL Stop Solution. Read at 450nm immediay.
 
[ REAGENTS AND MATERIALS PROVIDED ]
Reagents                                                                  Quantity
Pre-coated, ready to use 96-well strip plate            1
Plate sealer for 96 wells                                             4
Standard (lyophilized)                                                  2
Standard Diluent                                                       1×20mL
Detection Reagent A (green)                                  1×120μL
Assay Diluent A (2 × concentrate)                          1×6mL
Detection Reagent B (red)                                       1×120μL
Assay Diluent B (2 × concentrate)                         1×6mL
TMB Substrate                                                           1×9mL
Stop Solution                                                             1×6mL
Wash Buffer (30 × concentrate)                             1×20mL
Instruction manual                                                      1
 
[ STORAGE OF THE KITS ]
1. For unopened kit: All the reagents should be kept according to the labels on vials. The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20oC upon receipt while the others should be at 4 oC.
2. For opened kit: When the kit is opened, the remaining reagents still need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and reseal along entire edge of zip-seal.
Note:
It is highly recommended to use the remaining reagents within 1 month provided this is within the expiration date of the kit.
 
Note:
1. Samples to be used within 5 days may be stored at 4oC, otherwise samples must be stored at -20oC (≤1month) or -80oC (≤2 months) to avoid loss of bioactivity and contamination.
2. Sample hemolysis will influence the result, so hemolytic specimen can not be detected.
3. When performing the assay, bring samples to room temperature.

免責(zé)聲明

  • 凡本網(wǎng)注明“來(lái)源:化工儀器網(wǎng)”的所有作品,均為浙江興旺寶明通網(wǎng)絡(luò)有限公司-化工儀器網(wǎng)合法擁有版權(quán)或有權(quán)使用的作品,未經(jīng)本網(wǎng)授權(quán)不得轉(zhuǎn)載、摘編或利用其它方式使用上述作品。已經(jīng)本網(wǎng)授權(quán)使用作品的,應(yīng)在授權(quán)范圍內(nèi)使用,并注明“來(lái)源:化工儀器網(wǎng)”。違反上述聲明者,本網(wǎng)將追究其相關(guān)法律責(zé)任。
  • 本網(wǎng)轉(zhuǎn)載并注明自其他來(lái)源(非化工儀器網(wǎng))的作品,目的在于傳遞更多信息,并不代表本網(wǎng)贊同其觀點(diǎn)和對(duì)其真實(shí)性負(fù)責(zé),不承擔(dān)此類作品侵權(quán)行為的直接責(zé)任及連帶責(zé)任。其他媒體、網(wǎng)站或個(gè)人從本網(wǎng)轉(zhuǎn)載時(shí),必須保留本網(wǎng)注明的作品第一來(lái)源,并自負(fù)版權(quán)等法律責(zé)任。
  • 如涉及作品內(nèi)容、版權(quán)等問(wèn)題,請(qǐng)?jiān)谧髌钒l(fā)表之日起一周內(nèi)與本網(wǎng)聯(lián)系,否則視為放棄相關(guān)權(quán)利。
企業(yè)未開(kāi)通此功能
詳詢客服 : 0571-87858618
在线成色中文综合网站-国产二区精品视频在线观看| 交换朋友的妻子中文字幕-日本美女8x8x8x8| 欧美亚洲另类久久久精品-国产精品一区二区亚洲推荐| 欧美精品午夜一二三区-a屁视频一区二区三区四区| 两性污污视频网站在线观看-亚洲欧美日韩激情一区| 中文字幕亚洲中文字幕-丰满老妇伦子交尾在线播放| 日本高清二区视频久二区-大香蕉在线视频大香蕉在线视频| 久久特一级av黄色片-91社区视频免费观看| 日韩毛片在线免费人视频-超碰中文字幕av在线| 欧美精品午夜一二三区-a屁视频一区二区三区四区| 欧美精品啪啪人妻一区二区-嫩草人妻舔舔羞羞一区二区三区| 久久久国产精品电影片-精品孕妇人妻一区二区三区| 日韩中文字幕v亚洲中文字幕-日韩亚洲av免费在线观看| 在线观看中午中文乱码-2021国产一级在线观看| 亚洲精品激情一区二区-久久成人国产欧美精品一区二区| 国产一级片久久免费看同-麻豆精品尤物一区二区青青| 黄色美女网站大全中文字幕-欧美韩国日本一区二区| 欧美日韩黑人在线播放-51在线精品免费视频观看| 欧美日韩精品人妻在线-在线播放中文字幕一区| 日本韩国亚洲欧美三级-日本东京不卡网一区二区三区| 婷婷综合在线视频观看-亚洲一区二区三区香蕉| 亚洲黑人欧美一区二区三区-亚洲一区二区三区免费视频播放| 久久网站中文字幕精品-三级精品久久中文字幕| 日韩亚洲欧美综合在线-成人在线网站在线观看| 亚洲国产中文欧美一区二区三区-国产精品一区二区视频成人| 黄色美女网站大全中文字幕-欧美韩国日本一区二区| 日本高清二区视频久二区-大香蕉在线视频大香蕉在线视频| 国产高清av免费在线观看-黄片毛片大全一区二区三区| 丝袜美腿人妻连续中出-在线观看日韩三级视频| 色婷婷六月婷婷一区二区-91草草国产欧美在线观看| 亚洲黑人欧美一区二区三区-亚洲一区二区三区免费视频播放| 国产小黄片高清在线观看-涩涩鲁精品亚洲一区二区| av网址在线直接观看-黄色av全部在线观看| 欧美一级一线在线观看-亚洲一区二区亚洲三区| 日韩亚洲欧美综合在线-成人在线网站在线观看| 国产精品久久久精品一区-99久久免费精品国产男女性高好| 国产美女裸露无遮挡双奶网站-国产精品色午夜视频免费看| 国产午夜精品理论片A级漫画-久久精品国产99亚洲精品| 熟妇勾子乱一区二区三区-欧美爱爱视频一区二区| av一区免费在线观看-中文字幕日韩国产精品视频| 日韩二级视频在线观看-美女扒开奶罩露出奶子的视频网站|