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GE28-9042-59Analysis Note To view the Certificate of Analysis for this product, please visit www.cytiva.
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GE28-9042-58Analysis Note To view the Certificate of Analysis for this product, please visit www.cytiva.
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420298-100UG
Sigma-Aldrich
INSOLUTION K-252A NOCARDIOPSIS SP. - CAS 97161-97-2 - CALBIOCHEM
Price: $435.31List Price: $483.67A cell-permeable, reversible, and ATP-competitive inhibitor against multiple protein kinases, including, but not limited to, CaM kinase II (K i = 1.8 nM), myosin light chain kinase (K i = 20 nM), protein kinase A (K i = 18 nM), protein kinase C (K -
420297-100UG
Sigma-Aldrich
InSolution K-252a, Nocardiopsis sp. - CAS 97161-97-2 - Calbiochem
Price: $450.00List Price: $500.00A cell-permeable protein kinase inhibitor that inhibits CaM kinase II (K i = 1.8 nM), myosin light chain kinase (K i = 17 nM), protein kinase A (K i = 18 nM), protein kinase C (K i = 25 nM), and protein kinase G (K i = 20 nM). -
412400-10MGA cell-permeable tetrahydroisoquinolinylidene compound that modulates Wnt/β-catenin signaling by targeting the PR72/130 subunit of PP2A and thereby blocking PP2A/Nkd complex formation, resulting in diminished β-catenin/p300 interaction
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88052041-1VLHomozygous: Yes Cell Line Description This cell line is an Epstein-Barr Virus (EBV) transformed lymphoblastoid line and is part of the Human Leukocyte Antigen (HLA) Typed Collection maintained by the European Collection of Cell Cultures (ECACC).
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J413666-100mg​JND3229 JND3229 is a potent reversible inhibitor of EGFR C797S with an IC50 value of 5.8 nM. JND3229 also potently suppresses EGFR L858R/T790M and EGFR WT with IC50 values of 30.5 nM and 6.8 nM, respectively.
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J413666-10mg​JND3229 JND3229 is a potent reversible inhibitor of EGFR C797S with an IC50 value of 5.8 nM. JND3229 also potently suppresses EGFR L858R/T790M and EGFR WT with IC50 values of 30.5 nM and 6.8 nM, respectively.
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J4649-1MGBiochem/physiol Actions JNJ-10198409 is a potent ATP-competitive inhibitor of Platelet-Derived Growth Factor receptor tyrosine kinase (PDGF-RTK) with both antiangiogenic and a direct tumor cell antiproliferative activity. It is selective for
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J3770-25MGApplication JNJ7777120 has been used as a histamine-4 receptor antagonist: to study its effects on the pro-inflammatory microglia in rats to study its effects on the Parkinson′s-like pathology in rat brain to study its effects on the
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J3770-5MGApplication JNJ7777120 has been used as a histamine-4 receptor antagonist: to study its effects on the pro-inflammatory microglia in rats to study its effects on the Parkinson′s-like pathology in rat brain to study its effects on the
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J4252-25MGApplication JWH-015 has been used to study its effect on tumor-evoked pain behavior. It has also been used to study its protective effects on rat brain mitochondria upon paraquat exposure.