更新時(shí)間:2022-08-11
上海恒過生物長期代理美國進(jìn)口分裝、原裝ELISA“人胎盤蛋白(PP)",現(xiàn)貨供應(yīng),*,質(zhì)量保證。中英文雙版說明書,公司提供免費(fèi)代測服務(wù)。歡迎您來電來涵.
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試劑名稱:人胎盤蛋白(PP)
英文名稱:Human placental protein,PP ELISA KIT
檢測范圍:詳見說明書
產(chǎn)品規(guī)格:96人份/48人份
檢測目標(biāo):人、大小鼠、豬、豚鼠、雞、羊、兔...
保存條件: 2-8℃
應(yīng)用范圍:科研用檢測試劑
人胎盤蛋白(PP)相關(guān)產(chǎn)品:
人β細(xì)胞素ELISA試劑盒 Human beta cellulin,BTC ELISA KIT
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人胎盤核糖核酸抑止劑ELISA試劑盒 Human placental ribonuclease inhibitor,HPRI ELISA KIT
人胎盤蛋白ELISA試劑盒 Human placental protein,PP ELISA KIT
人胎盤催乳素ELISA試劑盒 Human placenta lactogen,HPL ELISA KIT
人胎兒血紅蛋白ELISA試劑盒 Human fetal hemoglobin,HBF ELISA Kit
人抗巨細(xì)胞病毒抗體IgMELISA試劑盒 Human anti-cytomegalovirus IgM antibody,anti-CMV IgM ELISA KIT
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Assay procedure(操作步驟)
1.Dilute and add sample:Dilute Original density Standard as follow table:
8 pg/ml 5 Standard 150μl Original density Standard+150μl Standard diluent
4pg/ml 4 Standard 150μl 5 Standard+150μl Standard diluent
2 pg/ml 3 Standard 150μl 4 Standard+150μl Standard diluent
1 pg/ml 2 Standard 150μl 3 Standard +150μl Standard diluent
0.5 pg/ml 1 Standard 150μl 2 Standard +150μl Standard diluent
2.add sample:Set blank wells separay (blank comparison wells don’t add sample and HRP-
Conjugate reagent, other each step operation is same). testing sample well. add Sample
dilution 40μl to testing sample well, then add testing sample 10μl (sample final
dilution is 5-fold), add sample to wells , don’t touch the well wall as far as
possible, and Gently mix.
3.Incubate: After closing plate with Closure plate membrane ,incubate for 30 min at 37℃.
4.Configurate liquid: 30-fold wash solution diluted 30-fold (or 20-fold) with distilled
water and reserve.
5.washing:Uncover Closure plate membrane, discard Liquid, dry by swing, add washing buffer
to every well, still for 30s then drain, repeat 5 times, dry by pat.
6.add enzyme:Add HRP-Conjugate reagent 50μl to each well, except blank well.
7.incubate:Operation with 3.
8.washing:Operation with 5.
9.color:Add Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the
light preservation for 15 min at 37℃
10.Stop the reaction:Add Stop Solution50μl to each well, Stop the reaction(the blue color
change to yellow color).
11.assay:take blank well as zero , Read absorbance at 450nm after Adding Stop Solution
and within 15min.
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