Data underlying the research of: The mRNA expression of CACYBP in bladder and kidney cancer.
DOI: 10.4121/22004108
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Dataset
qRT-PCR
Cellular RNA was extracted using Trizol, and total RNA (500 ng) was transcribed into cDNA using the PrimeScript kit. Actin primers were used as an internal control. Real-time fluorescence quantitative RT-PCR assays were performed using Lightcycler 480ii. The qRT-PCR primer sequences used in this study are shown below: Cacybp: forward primer: 5-CTCCCATTACAACGGGCTATAC-3, reverse primer: 5-GAACTGCCTTCCACAGAGATG-3; hactin: forward primer: 5-GGCATCGTCACCAACTGGGAC-3; reverse primer: 5-CGATTTCCCGCTCGGCCGTGG-3. Obtain the Cq datas of the actin and CACYBP gene of HK-2, O-786, SV-HUC-1, T24 cells for analysis.
History
- 2023-02-08 first online, published, posted
Publisher
4TU.ResearchDataFormat
*.xlsOrganizations
The Affiliated Hospital of Qingdao University, Department of Urology, ChinaDATA
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