上海博研生物工程研究中心竭誠(chéng)為您提供的產(chǎn)品和服務(wù)，期待您的來(lái)電,Elisa試劑盒，Elisa試劑盒說(shuō)明書，Elisa試劑盒價(jià)格

產(chǎn)品名稱：雞生長(zhǎng)因子（GH）ELISA試劑盒科研    
英文名稱：Chicken growth hormone,GH  ElisaKit.
產(chǎn)品編號(hào)：BYS12655B
產(chǎn)品性狀：液體
產(chǎn)品用途：科研實(shí)驗(yàn)
產(chǎn)品規(guī)格：96T/48T

ELISA實(shí)驗(yàn)原理: 用純化的抗體包被微孔板，制成固相載體，往包被抗體的微孔中依次加入標(biāo)本或者標(biāo)準(zhǔn)品、*化的抗體、HRP-標(biāo)記的親和素，經(jīng)過(guò)*洗滌后用底物顯色。底物在過(guò)氧化物酶的催化下轉(zhuǎn)化成藍(lán)色， 并在酸的作用下轉(zhuǎn)化成zui終的黃色。 顏色的深淺和樣品中的目標(biāo)蛋白呈正相關(guān)。用酶標(biāo)儀在（450nm）波長(zhǎng)下測(cè)定測(cè)定O.D.值（吸光度），計(jì)算樣品濃度。.

雞生長(zhǎng)因子（GH）ELISA試劑盒科研  相關(guān)產(chǎn)品：

人抗IVIgG抗體試劑盒說(shuō)明書，96T/48T*
人抗心肌抗體（AMA）試劑盒說(shuō)明書，96T/48T*
人碳酸酐酶（CA）試劑盒說(shuō)明書，96T/48T*
人β血小板球蛋白/β血栓環(huán)蛋白（β-TG）試劑盒說(shuō)明書，96T/48T*
人抗*（AT）試劑盒說(shuō)明書，96T/48T*
人抗核糖體P蛋白抗體（ARPA/Rib-P）試劑盒說(shuō)明書，96T/48T*
人組蛋白H2b（histon-H2b）試劑盒說(shuō)明書，96T/48T*
人甲狀腺球蛋白（TG）試劑盒說(shuō)明書，96T/48T*
人抗線粒體抗體（AMA）試劑盒說(shuō)明書，96T/48T*
人可提取核抗原（ENA）試劑盒說(shuō)明書，96T/48T*
兔子S100蛋白（S-100）試劑盒說(shuō)明書，96T/48T*
兔主要組織相容性復(fù)合體Ⅱ類（MHCⅡ/RLAⅡ）試劑盒說(shuō)明書，96T/48T*
兔子*受體（TR）試劑盒說(shuō)明書，96T/48T*
兔子可溶性P選擇素（sP-selectin）試劑盒說(shuō)明書，96T/48T*
兔子Ⅰ型前膠原羧基端肽（PⅠCP）試劑盒說(shuō)明書，96T/48T*
兔子Ⅰ型膠原（Col Ⅰ）試劑盒說(shuō)明書，96T/48T*
兔子Ⅱ型膠原（Col Ⅱ）試劑盒說(shuō)明書，96T/48T*
兔子Ⅲ型前膠原肽（PⅢNP）試劑盒說(shuō)明書，96T/48T*
兔子Ⅲ型前膠原氨基端肽（PⅢNT）試劑盒說(shuō)明書，96T/48T*
兔子*Ⅱ（FⅡ）試劑盒說(shuō)明書，96T/48T*

The microtiter plate provided in ELISA Kit has been precoated with an antibody specific to the target protein. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated specific polyclonal antibody preparation,and Avidincon jugated to Horseradish Peroxidase（HRP） is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain target protein, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of the samples is then determined by comparing the O.D. of the samples to the standard curve