Log In Sign up
The largest database of trusted experimental protocols

Human usp13 sirna

Manufactured by Merck Group
Visit Supplier
Sourced in United States

Human USP13 siRNA is a laboratory reagent designed for use in RNA interference (RNAi) research. It is a short, double-stranded RNA molecule that targets the USP13 gene, which encodes the deubiquitinating enzyme Ubiquitin Specific Peptidase 13. This product is intended for research use only and its specific applications should be determined by the user.

Automatically generated - may contain errors

Lab products found in correlation

Control sirna, by Merck Group (2 mentions) Pepmute sirna transfection reagent, by SignaGen (1 mentions) Genmute sirna transfection reagent, by SignaGen (1 mentions)

Spelling variants of this product

SiRNAs (112 citations)

2 protocols using human usp13 sirna

1

Transfecting TXNIP Plasmids and siRNA

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human USP13 siRNA and control siRNA were purchased from Sigma Aldrich (St Louis, MO, USA). Cells were cultured on 60-mm dishes to 70–90% confluence. Plasmids encoding HA-tagged human TXNIP and TXNIP-S308A, empty vector, and siRNAs were transfected into IMR90 cells using PepMute™ siRNA transfection reagent or GenJet™ DNA transfection reagents (SignaGen, Rockville, MD) according to the transfection reagent manufacturer’s instructions.
Taleb S.J., Ye Q., Baoyinna B., Dedad M., Pisini D., Parinandi N.L., Cantley L.C., Zhao J, & Zhao Y. (2024). Molecular Regulation of Transforming Growth Factor-β1-induced Thioredoxin-interacting Protein Ubiquitination and Proteasomal Degradation in Lung Fibroblasts: Implication in Pulmonary Fibrosis. Journal of respiratory biology and translational medicine, 1(1), 10002.
+ Open protocol
+ Expand
2

USP13 siRNA and Plasmid Transfection

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
GenMute siRNA transfection reagent and LipoJet DNA transfection reagents were purchased from SignaGen (Rockville, MD, USA). Human Usp13 siRNA and control siRNA were purchased from Sigma Aldrich (St Louis, MO, USA). Cells were cultured on 6-well plates or 10-mm dishes to 70%−90% confluence. Plasmid encoding V5-tagged human USP13,22 (link) empty vector, and siRNAs were transfected into Mrc5 cells according to the transfection reagent manufacturer’s instructions.
Li Y, & Kornberg R.D. (1994). Interplay of positive and negative effectors in function of the C-terminal repeat domain of RNA polymerase II.. Proceedings of the National Academy of Sciences of the United States of America, 91(6), 2362-2366.
+ 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!