Lab Reagents
Allelebio Laboratories manufactures the was bi reagents distributed by Genprice. The Was Bi reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Allelebio. Other Was products are available in stock. Specificity: Was Category: Bi
Serum / Plasma information
BI-D1870 |
B2227-10 |
ApexBio |
10 mg |
EUR 270 |
Description: BI-D1870 is a cell-permeable inhibitor of the p90 RSK isoforms with IC50 values of 31nM, 24nM, 18nM and 15nM for RSK1, RSK2, RSK3 and RSK4 respectively [1].BI-D1870 is a derivative of dihydropteridinone and found to be a remarkably specific inhibitor of RSK isoforms. |
BI-D1870 |
B2227-5 |
ApexBio |
5 mg |
EUR 189 |
Description: BI-D1870 is a cell-permeable inhibitor of the p90 RSK isoforms with IC50 values of 31nM, 24nM, 18nM and 15nM for RSK1, RSK2, RSK3 and RSK4 respectively [1].BI-D1870 is a derivative of dihydropteridinone and found to be a remarkably specific inhibitor of RSK isoforms. |
BI-D1870 |
B2227-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 235 |
Description: BI-D1870 is a cell-permeable inhibitor of the p90 RSK isoforms with IC50 values of 31nM, 24nM, 18nM and 15nM for RSK1, RSK2, RSK3 and RSK4 respectively [1].BI-D1870 is a derivative of dihydropteridinone and found to be a remarkably specific inhibitor of RSK isoforms. |
BI-D1870 |
B2227-50 |
ApexBio |
50 mg |
EUR 595 |
Description: BI-D1870 is a cell-permeable inhibitor of the p90 RSK isoforms with IC50 values of 31nM, 24nM, 18nM and 15nM for RSK1, RSK2, RSK3 and RSK4 respectively [1].BI-D1870 is a derivative of dihydropteridinone and found to be a remarkably specific inhibitor of RSK isoforms. |
BI 6015 |
B5668-10 |
ApexBio |
10 mg |
EUR 179 |
Description: BI 6015 is an antagonist of hepatocyte nuclear factor 4? [1]. Hepatocyte nuclear factor 4? (HNF4?) is a nuclear receptor and regulates gene expression in enterocytes, hepatocytes and pancreatic ? cells [1]. BI 6015 is a HNF4? antagonist. |
BI 6015 |
B5668-5 |
ApexBio |
5 mg |
EUR 118 |
Description: BI 6015 is an antagonist of hepatocyte nuclear factor 4? [1]. Hepatocyte nuclear factor 4? (HNF4?) is a nuclear receptor and regulates gene expression in enterocytes, hepatocytes and pancreatic ? cells [1]. BI 6015 is a HNF4? antagonist. |
BI 6015 |
B5668-50 |
ApexBio |
50 mg |
EUR 595 |
Description: BI 6015 is an antagonist of hepatocyte nuclear factor 4? [1]. Hepatocyte nuclear factor 4? (HNF4?) is a nuclear receptor and regulates gene expression in enterocytes, hepatocytes and pancreatic ? cells [1]. BI 6015 is a HNF4? antagonist. |
BI-847325 |
B6014-1 |
ApexBio |
1 mg |
EUR 132 |
Description: BI 847325 is a dual inhibitor of Ras-mitogen-activated protein kinase kinases (MEK) and Aurora kinases [1,2]. BI 847325 inhibits MEK1 and MEK2 with IC50 values of 25 and 4 nM, respectively. |
BI-847325 |
B6014-5 |
ApexBio |
5 mg |
EUR 242 |
Description: BI 847325 is a dual inhibitor of Ras-mitogen-activated protein kinase kinases (MEK) and Aurora kinases [1,2]. BI 847325 inhibits MEK1 and MEK2 with IC50 values of 25 and 4 nM, respectively. |
BI-9564 |
B6184-1 |
ApexBio |
1 mg |
EUR 109 |
Description: IC50: 75 nM and 3.4 ?M for BRD9 and BRD7 bromodomains, respectivelyBI-9564 is a BRD9/7 specific inhibitor.BRD7 and BRD9 are two important members of the bromodomain family protein. |
BI-9564 |
B6184-10 |
ApexBio |
10 mg |
EUR 293 |
Description: IC50: 75 nM and 3.4 ?M for BRD9 and BRD7 bromodomains, respectivelyBI-9564 is a BRD9/7 specific inhibitor.BRD7 and BRD9 are two important members of the bromodomain family protein. |
BI-7273 |
B6196-25 |
ApexBio |
25 mg |
EUR 437 |
Description: IC50: 19 and 117 nM for BRD9 and BRD7, respectively.BI-7273 is a BRD9 bromodomain inhibitor. |
BI-7273 |
B6196-5 |
ApexBio |
5 mg |
EUR 168 |
Description: IC50: 19 and 117 nM for BRD9 and BRD7, respectively.BI-7273 is a BRD9 bromodomain inhibitor. |
BI 78D3 |
B9011-10 |
ApexBio |
10 mg |
EUR 216 |
Description: BI-78D3 is a substrate competitive inhibitor of JNK inhibitor [2].JNK is a member of the MAPK family. JNK is a stress-activated protein kinase that modulates pathways implicated in a variety of disease states. |