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人血紅素氧化酶2(HO-2)ELISA試劑盒現(xiàn)貨
點(diǎn)擊次數(shù):2發(fā)布時(shí)間:2016/8/13 15:21:12

更新日期:2016/8/13 15:21:12
所 在 地:中國大陸
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詳細(xì)內(nèi)容
ELISA 檢測的目的是為實(shí)驗(yàn)提供準(zhǔn)確可靠的定量分析實(shí)驗(yàn)依據(jù)。為了保證實(shí)驗(yàn)數(shù)據(jù)的可靠性,在實(shí)驗(yàn)過程中必須堅(jiān)持全面質(zhì)量控制和全過程質(zhì)量控制。在收集標(biāo)本前都必須有一個(gè)完整的計(jì)劃。齊一生物銷售:021-6034 8496;181214 53965;173021 04490
注意事項(xiàng):
◆ 每個(gè)標(biāo)本量收集體積= 100ul × 檢測種類,如要做復(fù)孔,標(biāo)本量收集體積= 100ul × 檢測種類×2 。
◆ 對于作某一個(gè)具體指標(biāo)來說,先用一系列稀釋度作一批標(biāo)本測定,得出對實(shí)驗(yàn)有意義的一個(gè)稀釋度(即測定劑量反應(yīng)曲線),然后用一個(gè)*適稀釋度測定即可。
◆ 收集標(biāo)本前必須清楚要檢測的成份是否足夠穩(wěn)定。對收集后當(dāng)天進(jìn)行檢測的標(biāo)本,儲存在4℃?zhèn)溆茫缬刑厥庠蛐枰芷谑占瘶?biāo)本,將標(biāo)本及時(shí)分裝后放在-20℃ 或-70℃ 條件下保存。避免反復(fù)凍融。標(biāo)本 2 -8 ℃ 可保存48 小時(shí).-20℃ 可保存1個(gè)月。 -70 度可保存6個(gè)月。部分激素類標(biāo)本需添加抑肽酶。
◆ 血清標(biāo)本采集時(shí),應(yīng)注意避免溶血,紅細(xì)胞溶解時(shí)會釋放出具有過氧化物酶活性的物質(zhì),以 HRP為標(biāo)記的 ELISA 測定中,溶血標(biāo)本可能會增加非特異性顯色。
【人血紅素氧化酶2(HO-2)ELISA試劑盒現(xiàn)貨】◆ 為了保證尿液檢測結(jié)果的準(zhǔn)確性,必須正確收集尿液標(biāo)本和保存。盛尿容器要清潔干燥。使用一次性的容器(如塑料尿杯),避免因用藥并清洗不干凈而造成的污染,影響檢測結(jié)果。尿液標(biāo)本必須新鮮,留取后,應(yīng)及時(shí)檢測或保存,以免細(xì)菌繁殖。因在室溫中久置后(尤其是夏季)尿中磷酸鹽等可析出結(jié)晶而干擾檢測。
◆ 標(biāo)本宜在新鮮時(shí)檢測。如有細(xì)菌污染,菌體中可能含有內(nèi)源性 HRP,也會產(chǎn)生假陽性反應(yīng)。保存過久可發(fā)生聚合在 ELISA中可使本底加深。
◆ 凍結(jié)標(biāo)本融解后,蛋白質(zhì)局部濃縮,分布不均,應(yīng)充分混勻宜輕緩,避免氣泡,可上下顛倒混和,不要在混勻器上強(qiáng)烈振蕩。
◆ 混濁或有沉淀的標(biāo)本應(yīng)先離心或過濾,澄清后再檢測。
◆ 反復(fù)凍融會使蛋白效價(jià)降低,所以待測標(biāo)本如需保存作多次檢測,宜少量分裝冰存。也可加入適當(dāng)防腐劑。
◆ 如果您在實(shí)驗(yàn)中遇到任何特殊問題,敬請咨詢 021-60348496標(biāo)本類型
ELISA常見的標(biāo)本一般包括:
◆ 液體類標(biāo)本:包括血清、血漿、尿液、胸腹水、腦脊液、細(xì)胞培養(yǎng)上清等。
◆ 培養(yǎng)細(xì)胞
◆ 組織標(biāo)本
這些標(biāo)本收集的時(shí)間、方法和保存都有一定的要求。
【人血紅素氧化酶2(HO-2)ELISA試劑盒現(xiàn)貨】標(biāo)本的保存
一般說來,在 5 天內(nèi)測定的標(biāo)本可放置于 4℃,超過一周測定的需低溫凍存。
對收集后當(dāng)天進(jìn)行檢測的標(biāo)本,儲存在 4 ℃ 備用,如有特殊原因需要周期收集標(biāo)本, 將標(biāo)本及時(shí)分裝后放在 -20 ℃ 或 -70 ℃ 條件下保存。避免反復(fù)凍融。 標(biāo)本 2 -8 ℃ 可保存 48 小時(shí),-20 ℃ 可保存 1 個(gè)月。-70 度可保存 6 個(gè)月。部分標(biāo)本也可加入適當(dāng)防腐劑,激素類標(biāo)本需添加抑肽酶。標(biāo)本的處理 可用作 ELISA 測定的標(biāo)本十分廣泛,體液(如血清)、分泌物(唾液)和排泄物(如尿液)、細(xì)胞培養(yǎng)上清、細(xì)胞、組織等均可作標(biāo)本以測定其中某種成份。有些標(biāo)本可直接進(jìn)行測定,有些則需經(jīng)預(yù)處理。
◆ 血清:
室溫血液自然凝固 10-20 分鐘后,離心 20 分鐘左右( 2000-3000 轉(zhuǎn) / 分)。收集上清。如有沉淀形成,應(yīng)再次離心。
◆ 血漿:
應(yīng)根據(jù)試劑盒的要求選擇 EDTA 、檸檬酸鈉或肝素作為抗凝劑,加入 10 %( v/v )抗凝劑 ( 0.1M 檸檬酸鈉或 1% heparin 或 2.0%EDTA.Na2) 混合 10-20 分鐘后,離心 20 分鐘左右( 2000-3000 轉(zhuǎn) / 分)。仔細(xì)收集上清如有沉淀形 成,應(yīng)再次離心。
【人血紅素氧化酶2(HO-2)ELISA試劑盒現(xiàn)貨】◆ 尿液、胸腹水、腦脊液:
用無菌管收集。離心 20 分鐘左右( 2000-3000 轉(zhuǎn) / 分)。仔細(xì)收集上清。如有沉淀形成,應(yīng)再次離心。
◆ 細(xì)胞培養(yǎng)上清:
檢測分泌性的成份時(shí),用無菌管收集。離心 20 分鐘左右( 2000-3000 轉(zhuǎn) / 分)。仔細(xì)收集上清。檢測細(xì)胞內(nèi)的 成份時(shí),用 PBS ( PH7.2-7.4 )稀釋細(xì)胞懸液,細(xì)胞濃度達(dá)到 100 萬 /ml 左右。通過反復(fù)凍融,以使細(xì)胞破壞并放出細(xì)胞內(nèi)成份。離心 20 分鐘左右( 2000-3000 轉(zhuǎn) / 分)。仔細(xì)收集上清。保存過程中如有沉淀形成,應(yīng)再次離心。
◆ 細(xì)胞:
檢測細(xì)胞的成份時(shí),對于貼壁細(xì)胞,去除培養(yǎng)液,用PBS、生理鹽水或無血清培養(yǎng)液洗一遍。加入適量裂解液。用槍吹打數(shù)下,使裂解液和細(xì)胞充分接觸。通常裂解液接觸細(xì)胞10 秒后,細(xì)胞就會被裂解。對于懸浮細(xì)胞,離心收集細(xì)胞,用PBS、生理鹽水或無血清培養(yǎng)液洗一遍.加入適量裂解液, 用槍吹打把細(xì)胞吹散。用手指輕彈以充分裂解細(xì)胞。充分裂解后應(yīng)沒有明顯的細(xì)胞沉淀。如果細(xì)胞量較多,必需分裝然后再裂解。充分裂解后,10000-14000g離心3-5 分鐘,取上
清,即可進(jìn)行后續(xù)操作。
【人血紅素氧化酶2(HO-2)ELISA試劑盒現(xiàn)貨】◆ 組織標(biāo)本:
切割標(biāo)本后,稱取重量。加入一定量的 PBS或組織蛋白萃取試劑,緩沖液中可加入蛋白酶抑制劑。用手工或勻漿器將標(biāo)本勻漿充分。離心 20 分鐘左右( 2000-3000 轉(zhuǎn) / 分)。仔細(xì)收集上清置于 -20 度或 - 70 度保存,如有必要,可以將樣品濃縮干燥。分裝后一份待檢測,其余冷凍備用。齊一生物銷售:021-6034 8496;181214 53965;173021 04490
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