product summary
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company name :
Alomone Labs
product type :
chemical
product name :
U0126
catalog :
U-400
more info or order :
citations: 2
Reference |
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Clauzure M, Valdivieso A, Massip Copiz M, Schulman G, Teiber M, Santa Coloma T. Disruption of interleukin-1? autocrine signaling rescues complex I activity and improves ROS levels in immortalized epithelial cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function. PLoS ONE. 2014;9:e99257 pubmed publisher
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image 2 :

Alomone Labs U0126 inhibits P42/44 MAPK phosphorylation via MEK1/MEK2 in C6 glioma cells. - Cells were grown to 70% confluence and serum starved for 1.5 h. The cells were then incubated for 2 h with various concentrations ofU0126(#U-400) and stimulated with 7 ng/ml PDGF-AA. Cell proteins were resolved by SDS-PAGE and probed with anti-phospho-P42/44 MAPK (upper panel) and with anti-P42/44 MAPK (lower panel). The phosphorylation of P42/44 decreased in a dose-dependent manner.
product information
CAT :
U-400
SKU :
U-400_1 mg
Product Name :
U0126
Group Type :
Non Antibodies
Product Type :
S. Molecules
Shipping and storage :
Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C
Product Page - Scientific background :
U0126 is a chemically synthesized organic compound that was initially recognized as a cellular AP-1 antagonist, and found to be a very selective and highly potent inhibitor of the Mitogen-Activated Protein Kinase (MAPK) cascade by inhibiting its immediate upstream activators, Mitogen-Activated Protein Kinase Kinase 1 and 2 (also known as MEK1 and MEK2, IC50: 70 and 60 nM respectively). U0126 inhibits both active and inactive MEK1,2, unlike PD098059 which only inhibits activation of inactive MEK1,2. Blockade of MEK activation would prevent downstream phosphorylation of a number of factors including p62TCF (Elk-1), an upstream inducer of c-Fos and c-Jun, components of the AP-1 complex.1-4Inhibition of the MEK/ERK pathway by U0126 also prevents all effects of oncogenic H-Ras and K-Ras, inhibits part of the effects triggered by growth factors and blocks the production of inflammatory cytokines and matrix metalloproteinases.5-11
Supplier :
Alomone Labs
Target :
MAPK Pathway
Long Description :
U0126 (#U-400) is a highly pure, synthetic, and biologically active compound.
Short Description :
A Specific MAPK Pathway Inhibitor
MW :
380.5
Source :
Synthetic
Molecular formula :
C18H16N6S2.
Effective Concentration :
0.1-100 µM.
Activity :
U0126 specifically inhibits the kinase activity of mitogen activated protein kinase kinase (MAPKK, MEK1 and MEK2). It is less toxic than PD 980591,2.
Reconstitution and Solubility :
DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
Solubility :
DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
Storage of solutions :
Up to two weeks at 4°C or six months at -20°C.Protect from light.
Lead Time :
1-2 Business Days
Country of origin :
Israel/IL
Applications key :
Application key: FC- Flow cytometry, IFC- Indirect flow cytometry, IHC- Immunohistochemistry,LCI- Live cell imaging, Calcium imaging assay,Cell survival assay, Electrophysiology, Neurite outgrowth assay.
Purity :
>99%
CAS No :
109511-58-2
Form :
Lyophilized Powder
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Chemical Name :
1,4-Diamino-2,3-dicyano-1,4-bis[2- aminophenylthio]butadiene.
more info or order :
company information

Alomone Labs
Jerusalem BioPark (JBP), Hadassah Ein Kerem
P.O. Box 4287
Jerusalem 9104201
P.O. Box 4287
Jerusalem 9104201
info@alomone.com
http://www.alomone.com972 2 531 8002
headquarters: Israel
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