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PD 98059


Poziom jakości







activity assay: suitable (kinase)


wet ice


Potent, selective and cell-permeable inhibitor of MAPK kinase, MAPK/ERK, or MEKK.

Działania biochem./fizjol.

Inhibitor Type: Kinase

Postać fizyczna


Przechowywanie i stabilność

2 years at -20°C

Informacje prawne

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

Oświadczenie o zrzeczeniu się odpowiedzialności

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Kod klasy składowania

11 - Combustible Solids



Certyfikat analizy

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Certificate of Quality

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D R Alessi et al.
The Journal of biological chemistry, 270(46), 27489-27494 (1995-11-17)
PD 098059 has been shown previously to inhibit the dephosphorylated form of mitogen-activated protein kinase kinase-1 (MAPKK1) and a mutant MAPKK1(S217E,S221E), which has low levels of constitutive activity (Dudley, D. T., Pang, L., Decker, S. J., Bridges, A. J., and
Qize Wei et al.
Molecular biology of the cell, 13(2), 683-697 (2002-02-21)
We ectopically expressed the transcription factor Pitx2a, one of the Pitx2 isoforms, in HeLa cells by using a tetracycline-inducible expression system and examined whether Pitx2a was capable of modulating Rho GTPase signaling and altering the cell's cytoskeleton. Ectopic expression of
L Pang et al.
The Journal of biological chemistry, 270(23), 13585-13588 (1995-06-09)
The mitogen-activated protein kinase (MAP kinase) pathway is thought to play an important role in the actions of neurotrophins. A small molecule inhibitor of the upstream kinase activator of MAP kinase, MAP kinase kinase (MEK) was examined for its effect
Barbara Chiavarina et al.
Theranostics, 11(4), 1626-1640 (2021-01-08)
Colorectal cancer (CRC) cells are traditionally considered unresponsive to TGFβ due to mutations in the receptors and/or downstream signaling molecules. TGFβ influences CRC cells only indirectly via stromal cells, such as cancer-associated fibroblasts. However, CRC cell ability to directly respond

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