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Ras Products

The Ras proteins (H-Ras, N-Ras, and two splice variants of K-Ras) define a closely related family of 21 kDa GTPases that cycle between GTP-bound active and GDP-bound inactive states at the cytoplasmic face of the plasma membrane. Receptor tyrosine kinases and G-protein coupled receptors activate Ras, and effectors include Raf and PI 3-kinase. Activating mutations of Ras, which impair GTPase activity and stabilize the active state, are found in nearly one-third of all human cancers.

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23 results for "Ras" in Products

23 results for "Ras" in Products

Ras Products

The Ras proteins (H-Ras, N-Ras, and two splice variants of K-Ras) define a closely related family of 21 kDa GTPases that cycle between GTP-bound active and GDP-bound inactive states at the cytoplasmic face of the plasma membrane. Receptor tyrosine kinases and G-protein coupled receptors activate Ras, and effectors include Raf and PI 3-kinase. Activating mutations of Ras, which impair GTPase activity and stabilize the active state, are found in nearly one-third of all human cancers.

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Applications: WB
Reactivity: Human
Applications: IHC, WB
Reactivity: Human, Mouse, Rat, Zebrafish, Xenopus, +2 More
Applications: IHC, WB, ICC/IF
Reactivity: Human, Mouse

Recombinant Monoclonal Antibody

Applications: IHC, WB
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: WB, ICC/IF, Flow
Reactivity: Human, Mouse, Rat

Recombinant Monoclonal Antibody

Applications: WB
Reactivity: Human
Applications: WB, ELISA, ICC/IF
Reactivity: Human, Mouse, Rat

Recombinant Monoclonal Antibody

Applications: WB
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human, Mouse
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human

Ras signaling inhibitor; inhibits Ack1 and GCK

Leucyl-tRNA synthase (TRS)/Ras-related GTP-binding protein D (RagD) interaction inhibitor

Potent farnesyl diphosphate (FPP) synthase inhibitor

Selective KRAS Degrader (PROTAC®)

Inhibits KRas localization to the plasma membrane; also L-type calcium channel blocker

High affinity PDEδ-KRas interaction inhibitor; binds to PDEδ

Selectively kills mutant HRAS-expressing cells; glutathione peroxidase inhibitor; induces ferroptosis

Mutation-selective inhibitor of KRASG12C

Negative control for LC 2 (Cat. No. 7420)

PDEδ autophagy-tethering compound (ATTEC) Degrader

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