VCT cells were seeded in a 96-well plate and allowed to attach overnight. The cells were then transfected with pCR3.1-based plasmid, miR-10a-AA, miR-10a-TT, miR-10a-TT/AA, respectively. 48 hours later, cells were carried out by Cell-Light Edu Apollo DNA in vitro kit (RiboBio, Guangzhou, China) according to the manufacturer's protocol. Proliferative cells were visualized and imaged under a laser-scanning confocal microscope (CarlZeiss LSM 710 META, Germany). Proliferative cells and total cell number were counted in three fields (magnification ×400) selected in a random manner. The results were described as a ratio of the cell number with proliferative cells vs total cells.
Cell light edu apollo dna in vitro kit
Manufactured by RiboBio
Sourced in China
The Cell-Light Edu Apollo DNA in vitro Kit is a laboratory equipment product designed for DNA-related experiments. It provides the core function of visualizing and analyzing DNA samples in vitro.
Automatically generated - may contain errors
Lab products found in correlation
3 protocols using cell light edu apollo dna in vitro kit
1
Quantifying Cell Proliferation by Edu Assay
2
Cell Proliferation Measurement Assay
Check if the same lab product or an alternative is used in the 5 most similar protocols
+ Expand
Cell proliferation was also estimated using Cell-Light Edu Apollo DNA in vitro Kit (RiboBio, Guangzhou, China). Proliferative cells were visualized and imaged using a Zeiss LSM 510 META Laser Scanning Confocal Microscopy (Nikon, Tokyo, Japan). Proliferative cells were counted in different optical fields (magnification × 200) selected in a random manner and analyzed by the software of Image J.
3
Cell Proliferation Assay Using Confocal Microscopy
Check if the same lab product or an alternative is used in the 5 most similar protocols
+ Expand
Cell proliferation was also estimated using Cell-Light Edu Apollo DNA in vitro Kit (RiboBio, Guangzhou, China). Proliferative cells were visualized and imaged using a Zeiss LSM 510 META Laser Scanning Confocal Microscopy (Nikon, Tokyo, Japan). Proliferative cells were counted in different optical elds (magni cation ×200) selected in a random manner and analyzed by the software of Image J.
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required
Revolutionizing how scientists
search and build protocols!