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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. [provided by RefSeq, Jul 2008]
Related Diseases
AGE-RAGE Signaling Pathway in Diabetic Complications
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- Species Reactivity: Human
- Type: Mouse antibody
- Application: IHC
- Human Anti-THBD Recombinant Antibody (clone QBEND/40) (FAMAB-1268CQ)
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- Species Reactivity: Rabbit, Human
- Type: Human IgG1
- Application: WB, EM, FC, IF, IHC
- Rabbit Anti-THBD Recombinant Antibody (clone JB48-23) (MRO-1490-CN)
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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
- Human Anti-THBD Antibody (clone QBEND/40), mRNA (FAMAB-1268CQ-mRNA)
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- Species Reactivity: Rabbit, Human
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- Species Reactivity: Mouse, Rat
- Type: Rabbit IgG
- Application: WB
- Mouse Anti-THBD Recombinant Antibody (clone 2G1) (VS3-XY1513)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IP, IHC, FC
- Recombinant Anti-Mouse Thbd VHH Single Domain Antibody (NAB-1329-VHH)
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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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