Log In Sign up
The largest database of trusted experimental protocols

Trizol reaction solution

Manufactured by Thermo Fisher Scientific
Visit Supplier

TRIZOL reaction solution is a single-step RNA isolation reagent that facilitates the extraction and purification of total RNA from a variety of biological samples. It is designed to maintain the integrity of the extracted RNA for downstream applications.

Automatically generated - may contain errors

Lab products found in correlation

Spelling variants of this product

TRIzol (38370 citations) TRIzol solution (515 citations)

2 protocols using trizol reaction solution

1

Differential Gene Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Control and treated samples were collected using TRIZOL reaction solution (ThermoFisher). Library preparation and RNA sequencing were completed at Novagene (Beijing, China). The statistical difference in gene expression was determined by the adjusted P-value cutoff value of 0.05 and the fold change cutoff value of 2. To determine statistically significant enrichment, we use the GO-seq R package to perform gene ontology (GO) analysis of differentially expressed genes. The corrected P-value cutoff value is 0.05 at this time.
Lin K., Gao W., Chen N., Yang S., Wang H., Wang R., Xie F., Meng J., Lam E.W., Li S., Cheng W., Chen P., Wu H., Yan J., Jin D, & Jin B. (2022). Chronic Inflammation Pathway NF-κB Cooperates with Epigenetic Reprogramming to Drive the Malignant Progression of Glioblastoma. International Journal of Biological Sciences, 18(15), 5770-5786.
+ Open protocol
+ Expand
2

RNA-Seq Protocol for Differential Gene Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
Control and treated samples were collected using TRIZOL reaction solution (ThermoFisher). Library preparation and RNA sequencing were completed at Novagene (Beijing, China). The statistical difference in gene expression was determined by the adjusted P-value cutoff value of 0.05 and the fold change cutoff value of 2. To determine statistically signi cant enrichment, we use the GO-seq R package to perform gene ontology (GO) analysis of differentially expressed genes. The corrected P-value cutoff value is 0.05 at this time.
Lin K., Gao W., Chen N., Wang H., Wang R., Yang S., Xie F., Meng J., Lam E.W., Ma C., Li S., Ning K., Hao Y., Wu Z., Ge Q., Guo L., Cheng W., Chen P., Wu H., Yan J., Jin D., & Jin B. (2022). Targeting Cooperation of Chronic Inflammation with Epigenetic Reprogramming Triggers a Synthetic Lethality in Glioblastoma Multiforme.
+ Open protocol
+ Expand

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

Sign up now

Revolutionizing how scientists
search and build protocols!