About 6 results found for searched term "PKA" (0.052 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M14905 | PKA Inhibitor Fragment (6-22) amide TFA | PKA |
| PKI-(6-22)-amide TFA | ||
| PKA Inhibitor Fragment (6-22) amide TFA is an inhibitor of cAMP-dependent protein kinase A (PKA), with a Ki of 2.8 nM. PKA Inhibitor Fragment (6-22) amide TFA can significantly reverse low-level morphine antinociceptive tolerance in mice. | ||
| M31261 | Akt1&PKA-IN-1 | Akt |
| Akt1&PKA-IN-1 is a potent dual Akt/PKA inhibitor with IC50 values of 0.03 , 0.11 μM, and 9.8 μM for PKAa, Akt, and CDK2, respectively. Akt1&PKA-IN-1 is selective for cyclin-dependent kinase 2 (CDK2). | ||
| M50395 | PKA Substrate | PKA |
| PKA Substrate is a potent and selective substrate peptide of PKA that can be used to detect PKA activity. | ||
| M50399 | H1-7 (histone H1 phosphorylation site), PKA Substrate | PKA |
| H1-7 (histone H1 phosphorylation site), PKA Substrate, a synthetic polypeptide, can be used as PKA substrate. | ||
| M50401 | PKA Inhibitor Fragment (6-22) amide | PKA |
| PKA Inhibitor Fragment (6-22) amide is an inhibitor of cAMP-dependent protein kinase A (PKA), with a Ki of 2.8 nM. | ||
| M57227 | PKA-IN-1 | PKA |
| PKA-IN-1 is a potent and selective cyclic AMP-dependent protein kinase (PKA) catalytic subunit (cAK) inhibitor with an IC50 of 0.03 μM. | ||
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
