Thbd
The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia.
Species Reactivity: Rabbit, Human
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Species Reactivity: Human
Type: Rabbit IgG
Application: WB, IHC, IP
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Derivation: Phage display library
Species Reactivity: Human
Type: Rabbit IgG
Application: WB
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Derivation: Mouse
Species Reactivity: Human
Type: Mouse IgG1, κ
Application: WB, IP, IF, IHC, ELISA
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Species Reactivity: Rabbit, Human
Type: Human IgG1
Application: WB, EM, FC, IF, IHC
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Species Reactivity: Human
Type: Mouse antibody
Application: IHC
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Species Reactivity: Human
Type: Rabbit IgG
Application: ELISA
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Species Reactivity: Human
Type: Rabbit IgG
Application: ELISA
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Species Reactivity: Human
Type: Rabbit IgG
Application: WB, IF, IP
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Species Reactivity: Human
Type: Mouse IgG1
Application: WB, IP, IHC, FC
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Species Reactivity: Mouse
Type: Llama VHH
Application: IHC, ICC, FC, FA, FUNC
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Species Reactivity: Human
Type: Rabbit IgG
Application: ELISA, IHC
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Species Reactivity: Mouse, Rat
Type: Rabbit IgG
Application: WB
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For Research Use Only. Not For Clinical Use.