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The intestinal tissue collected from the chicken farm is very turbid when lysed with Trizol reagent, and the RNA yield is low. What should I do?

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Asked by:Labing7973 2026-04-27 Views 174 4 answers
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All Answers4
小
小小新手6851 2026-08-04
肠道组织建议取材前尽量清除内容物。杀鸡后取肠段,用预冷无RNA酶的PBS或生理盐水快速冲肠腔,外表面再用玻片轻刮掉粘液,吸水纸吸干后剪碎入Trizol。不要反复冻融。粘液蛋白多,可以先加1mL Trizol匀浆后再补0.5mL,控制在1.5mL/50-80mg组织左右;裂解液过多反而氯仿分层变差。匀浆用中等转速、短时冰浴。
T
Tom3509 2026-07-04
中间层厚是肠道组织蛋白、多糖和脂肪混合造成的。离心后取上清别追求多,留1-2mm避免碰到中间层;如果上清仍浑浊,可以转移到新管,加等体积氯仿再涡旋离心一次。RNA得率低有时是取上清太保守,大量水相被丢弃,或者异丙醇沉淀后洗涤时把沉淀吸掉。可以加糖原助沉,并在-20℃延长沉淀到30-60min。
质
质控小哥 2026-07-02
肠道组织RNA降解快,两三百ng/mg在十二指肠和空肠不算很高,但要看RIN或电泳。如果现场来不及,最好取材后立刻液氮速冻或放RNAlater,统一提取。Trizol裂解后浑浊并不代表失败,很多肠道样本都这样。若比值不稳,建议后续联合柱式纯化:Trizol氯仿分相后取上清,加70%乙醇上RNA结合柱洗脱,能去除粘液多糖和蛋白。
R
Research4593 2026-09-22
Trizol和柱式联用对肠道样本会更稳定,尤其下游做菌群测序或转录组。可以先试用国产柱式RNA试剂盒做预实验,比较得率、260/230和RIN。国产裂解液也可以用,但肠道样本对裂解液去蛋白能力要求高,建议找供应商要试用装,不要直接大批量采购。如果只用Trizol,建议增加一次氯仿抽提、75%乙醇洗两次,比值会稳一些。
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