荧光定量PCR案例|人肝癌细胞基因表达分析
蛋白提取的核心在于最大限度地保持目标蛋白的完整性,防止其在提取过程中发生降解。因此,整个操作应在低温条件下进行,并尽量缩短处理时间。此外,针对不同来源的样本(如组织或细胞),需根据其特性选择合适的裂解液和提取方法。
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| 蛋白提取操作指南及注意事项 |
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[11141ES]Hifair® III 1st Strand cDNA Synthesis SuperMix for qPCR(gDNA digester plus)
[11149ES]Hifair® AdvanceFast 1st Strand cDNA Synthesis Kit
[11151ES]Hifair® AdvanceFast One-step RT-gDNA Digestion SuperMix for qPCR
[11155ES]Hifair® AdvanceFast 1st Strand cDNA Synthesis SuperMix for qPCR (DNA digester plus)
[11188ES]Hieff UNICON® ColorGPS qPCR SYBR Green Master Mix (No Rox)
[11189ES]Hieff UNICON® ColorGPS qPCR SYBR Green Master Mix (Low Rox)
[11190ES]Hieff UNICON® ColorGPS qPCR SYBR Green Master Mix (High Rox)
[11184ES]Hieff UNICON® Universal Blue qPCR SYBR Green Master Mix


