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product name 8-Bromo-cAMP


Description:  8-Bromo-cAMP is a cell perbeable cyclic AMP (cAMP) analog and a PKA activator. 8-Bromo-cAMP increased the cellular content of mRNA encoding the hCG a- and β-subunits and prevented the increase in fibronectin mRNA. This is determined by blot hybridization analysis using specific cDNA probes. 8-Bromo-cAMP also induced phosphorylation of Erk1,2 in AML193 cells. 8-Bromo-cAMP is an agent in AML193 cells and activates Erk1,2 , this condition happens does not accompanied by the involvement of Shc phosphorylation.

References: Stem Cell Rev. 2011 Jun;7(2):331-41; Am J Physiol Lung Cell Mol Physiol. 2014 Oct 15;307(8):L643-51. 



Molecular Weight (MW)

430.08 
Formula

C10H10BrN5NaO6
CAS No.

76939-46-3 
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 80 mg/mL (186.01 mM)
Water: < 1 mg/mL
Ethanol: 35 mg/mL (81.38 mM)
Solubility (In vivo)

 
Synonyms

 

other peoduct :

In Vitro

In vitro activity: 8-Bromo-cAMP improves the reprogramming efficiency of human neonatal foreskin fibroblast (HFF1) cells. In bronchial epithelial cells, 8-Bromo-cAMP decreases HDE-stimulated tumor necrosis factor (TNF)-α-converting enzyme (TACE; ADAM-17) activity and subsequent TNF-α release.


Kinase Assay:


Cell Assay: 8-Bromo-cAMP increased the cellular content of mRNA encoding the hCG a- and β-subunits and prevented the increase in fibronectin mRNA. This is determined by blot hybridization analysis using specific cDNA probes. 8-Bromo-cAMP also induced phosphorylation of Erk1,2 in AML193 cells. 8-Bromo-cAMP is an agent in AML193 cells and activates Erk1,2 , this condition happens does not accompanied by the involvement of Shc phosphorylation. 

In Vivo  
Animal model  
Formulation & Dosage  
References Stem Cell Rev. 2011 Jun;7(2):331-41; Am J Physiol Lung Cell Mol Physiol. 2014 Oct 15;307(8):L643-51.  

RVX-211

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Author: Sodium channel