SYBR Green Fast Advanced Cells-to-CT 试剂盒是一个完整的细胞裂解物系统,可直接根据培养细胞进行基因表达分析,而无需 RNA 纯化步骤。SYBR Green了解更多信息
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货号
反应次数
脱氧核糖核酸酶
A35381
400 次反应
220 μL DNase I
A35379
40 次反应
22 μL DNase I
A35380
100 次反应
55 μL DNase I
3 选项
货号 A35381
价格(CNY)
70,926.00
Each
添加至购物车
反应次数:
400 次反应
脱氧核糖核酸酶:
220 μL DNase I
价格(CNY)
70,926.00
Each
添加至购物车
SYBR Green Fast Advanced Cells-to-CT 试剂盒是一个完整的细胞裂解物系统,可直接根据培养细胞进行基因表达分析,而无需 RNA 纯化步骤。SYBR Green Fast Advanced Cells-to-CT 细胞裂解试剂提供了最高灵敏度的 Cells-to-CT Fast Advanced 逆转录酶混合物、2X RT 缓冲液和一流的 PowerUp SYBR Green预混液。SYBR Green Fast Advanced Cells-to-CT 试剂盒可在现有最快的工作流程中为您提供您所需的灵敏度:在约1.5小时内从整个细胞板中获得基因表达分析结果。
•全面—优化的工作流程包括移除 gDNA 的细胞裂解试剂、新型 Fast Advanced RT 酶混合物、缓冲液和新型 PowerUp SYBR Green Fast Advanced 预混液 •快速—7分钟样品制备,包括在室温下进行 DNase处理 •简便—可以在试管或直接在培养板中裂解样品 •稳健—可以对每个样品10–100,000个细胞进行基因表达分析;结果与从纯化 RNA 中获得的等效 •高效—含有足够的试剂以从100起始样品中生成1000实时荧光定量 PCR 结果
Will the Cells-to-CT system work with my special cell line?
There is no reason why the Cells-to-CT system shouldn’t work with any cell line. However, due to differences in cell size and composition, the maximum number of cells per lysis reaction may be slightly different for different cell lines. We recommend testing for inhibition and optimal cell input by using the TaqMan Cells-to-CT and SYBR Green Cells-to-CT Control kits.
Do the 2-step Cells-to-CT kits contain RNase inhibitor?
Yes, the Stop Solution provided in the 2-step Cells-to-CT kits contains RNase inhibitor.
Can I use the TaqMan Gene Expression Cells-to-CT kit for multiplexing?
The TaqMan Gene Expression Cells-to-CT kit has been validated for duplexing. If you want to set up a multiplex real-time PCR reaction with 3 assays, we recommend using the TaqMan Fast Advanced Cells-to-CT kit (https://www.thermofisher.com/order/catalog/product/A35374).
I am using a Cells-to-CT kit and I see signal from the genomic DNA in my real-time PCR results. How do I get rid of the genomic DNA contamination?
To prevent signal from genomic DNA in the Cells-to-CT real-time PCR reaction, we recommend using a TaqMan assay or primer set that spans an exon-exon boundary, and adding DNase I to degrade genomic DNA during the lysis reaction. For optimal DNase activity in the lysis reaction, we recommend the following:
1. Ensure all media is removed from the cells.
2. Wash each well or cell pellet with an equal volume of room temperature 1X PBS.
3. Ensure the lysis reaction happens at room temperature. The lysis reaction may not reach room temperature if the plate is on ice prior to adding Lysis Solution, or cold Lysis Solution is added.
4. Warm the Lysis Solution to room temperature before adding to the cells.
5. Perform the lysis reaction at 25 degrees C for up to 8 minutes.