Imiquimod, TLR7 ligand [NBP2-26228] - 293T cells were transfected with pCMV/TLR7 plasmid and pNF-kB/SEAP plasmid using Lipofectamin 2000. After 48 hrs of transfection, 5 ug/mL of Imiquimod (R-837) was added. Cells were ...read more
Product Details
Summary
Reactivity
Hu, MuSpecies Glossary
Applications
Func
Concentration
Please see the protocols for proper use of this product. If no protocol is available, contact technical services for assistance.
Imiquimod, TLR7 ligand is an imidazoquinoline amine analog to guanosine. As a synthetic molecule of the Imidazoquinoline family, it has potent immunostimulatory activity. Imiquimod has been shown to activate only TLR7. This activation is MyD88 dependant and leads to the induction of the transcription factor NF-kB.
Specificity
Imiquimod is human/mouse TLR7 agonist.
Endotoxin Note
<0.001 EU/ug
Applications/Dilutions
Dilutions
Functional
In vitro assay
Ligand Activation
Application Notes
Formula: C14H16N4, HCl. Molecular weight: 276.8. This product is useful for activation of TLR7 and stimulation of TLR7 has been achieved with 5-10 ug/mL. Use in ligand activation, functional, and in vitro assays reported in scientific literature (PMID 25957979)
Reviewed Applications
Read 1 Review rated 5 using NBP2-26228 in the following applications:
Publications
Read Publications using NBP2-26228 in the following applications:
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
NBP2-26228-0.125mg: 125 ug in 50 uL of DMSO (this product was formerly supplied in sterile water) NBP2-26228-1mg: 1 mg in 400 uL of DMSO.
Concentration
Please see the protocols for proper use of this product. If no protocol is available, contact technical services for assistance.
Notes
5 mg size will be provided as 5 x 1.0 mg vials.
Alternate Names for Imiquimod, TLR7 ligand
R 837
R837
Background
Imiquimod, TLR7 ligand, an imidazoquinoline amine analog to guanosine, is an immune response modifier with potent indirect antiviral activity. The antiviral activity of imiquimod was first shown in guinea pigs infected with herpes simplex virus [1]. Imiquimod is now an approved treatment for external genital warts caused by human papillomavirus infection. This low molecular synthetic molecule induces the production of cytokines such as IFN-Alpha. Unlike R848, Imiquimod activates only TLR7 but not TLR8 [2]. This activation is MyD88-dependent and leads to the induction of the transcription factor NF-kB [3].
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Support products are guaranteed for 6 months from date of receipt.
Publications for Imiquimod, TLR7 ligand (NBP2-26228)(13)
We have publications tested in 3 confirmed species: Human, Mouse, Chicken.
We have publications tested in 9 applications: Block/Neutralize, Flow Cytometry Control, Func, In Vivo, In vitro, In-vitro, Knockdown Validated, LA, Western Blot.
Imiquimod was added into the medium at final concentration of 10 μg/ml. Imiquimod enhanced the osteo-differentiation ability of mesenchymal stem cells.