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THBD

Anti-Thbd Products
- 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
- 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
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ELISA
- Human Anti-THBD Antibody (clone QBEND/40), mRNA (FAMAB-1268CQ-mRNA)
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- Species Reactivity: Rabbit, Human
- Mouse Anti-THBD Recombinant Antibody (clone 2G1) (VS3-XY1513)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IP, IHC, FC
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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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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: WB, IF, IP
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ELISA
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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: Human
- Type: Mouse antibody
- Application: IHC
- 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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- Derivation: Phage display library
- Species Reactivity: Human
- Type: Rabbit IgG
- Application: WB
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- Antibody Host: Human
- Antibody Reactivity: Human
- CytoStream™ Rat Anti-THBD Recombinant Antibody (VS-0225-XY207) (VS-0225-XY207)
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- Species Reactivity: Mouse
- Type: Rat IgG2a, kappa
- Application: FC
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- Species Reactivity: Rabbit, Human
- Target: THBD
- Host Animal: Human
- Application: ELISA, FC, Cell-uptake
- Anti-THBD Immunohistochemistry Kit (VS-0525-XY7228)
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- Species Reactivity: Human
- Target: THBD
- Application: IHC
- Anti-Mouse THBD Immunohistochemistry Kit (VS-0525-XY7229)
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- Species Reactivity: Mouse
- Target: THBD
- Application: IHC
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For Research Use Only. Not For Clinical Use.
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.