1μg (R: reducing condition, N:non-reducing condition).
Product Details
Product Details
Product Specification
| Species | Human |
| Synonyms | CD201, APC receptor, CCCA, CCD41 |
| Accession | Q9UNN8 |
| Amino Acid Sequence | Ser18-Ser210 with His Tag at the C-Terminus |
| Expression System | HEK293 |
| Molecular Weight | 35-40kDa (Reducing) |
| Purity | >95% by SDS-PAGE & HPLC |
| Conjugation | Unconjugated |
| Tag | His Tag |
| Physical Appearance | Lyophilized powder |
| Storage Buffer | PBS, pH7.4, 5% trehalose |
| Reconstitution | Reconstitute at 0.1-1 mg/ml according to the size in ultrapure water after rapid centrifugation. |
| Stability & Storage | · 12 months from date of receipt, lyophilized powder stored at -20 to -80℃. |
| Reference | 1. Wang H, March L, Jackson CJ, Cross M, Xue M. EPCR in Wound Healing: Mechanisms of Action and Therapeutic Potential. Cells. 2026 Mar 22;15(6):567. |
Background
EPCR (PROCR/CD201/activated protein C receptor) is a type I transmembrane N-glycosylated glycoprotein structurally related to the MHC class I/CD1 superfamily, featuring an extracellular domain with two α-helices and eight β-strands forming a hydrophobic lipid-binding groove. It is highly expressed on endothelial cells of arteries and veins in heart and lung, as well as on various stem/progenitor cells. Functionally, EPCR enhances protein C activation to APC by the thrombin-thrombomodulin complex, regulating coagulation; it also mediates cytoprotective signaling via PAR1, promoting cell proliferation, angiogenesis, and anti-inflammatory responses. A soluble form (sEPCR) is released by metalloproteases such as ADAM17. Clinically, EPCR represents a promising therapeutic target—its inhibition attenuates pathological retinal neovascularization, while APC-EPCR axis activation shows efficacy in wound healing, sepsis, and retinal protection, with non-anticoagulant APC variants being developed to minimize bleeding risks.
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SDS-PAGE
SEC-HPLC
The purity of EPCR/PROCR His Tag Protein, Human is more than 95% determined by SEC-HPLC.
