兔抗THBD多克隆抗体

Background:

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.

Applications:

WB

Name of antibody:

THBD

Immunogen:

Synthesized peptide derived from C-terminal of human THBD.

Full name:

thrombomodulin

Synonyms：

TM; THRM; AHUS6; BDCA3; CD141; THPH12

SwissProt:

P07204

WB Predicted band size:

60 kDa

WB Positive control:

K562 cells lysate

WB Recommended dilution:

500-3000