Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to
worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting
immunostaining in relation to complex human pathologies.
TCR Screening Services
Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding.
Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".
IHC, IHC - Paraffin, ICC, Immunofluorescence, Western blot
Sheep Polyclonal (IgG) to Human PROC / Protein C
Human PROC / Protein C
Human (tested or 100% immunogen sequence identity)
Specificity and Use
Human Protein C (PC) isolated from plasma.
Recognizes human Protein C as determined by immunoelectrophoresis and ELISA prior to conjugation. When tested against normal plasma a single arc was seen. No arc was seen with Protein C-deficient plasma.
Suitable for use in ELISA. The applications listed have been tested for the unconjugated form of this product. Other forms have not been tested.
Buffered stabilizer solution, 50% glycerol.
May be stored at 4°C for short-term only. Aliquot to avoid freeze-thaw cycles. Store at -20°C. Aliquots are stable for 1 year.
PROC Antibody, Anticoagulant protein C Antibody, Blood coagulation factor XIV Antibody, Autoprothrombin IIA Antibody, Protein C Antibody, PROC1 Antibody, Vitamin K-dependent protein C Antibody, THPH3 Antibody, THPH4 Antibody
PROC / Protein C is a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form by the thrombin-thrombomodulin complex. This activated form contains a serine protease domain and functions in degradation of the activated forms of coagulation factors V and VIII. Mutations in this gene have been associated with thrombophilia due to protein C deficiency, neonatal purpura fulminans, and recurrent venous thrombosis.