Radioimmunoassay of factor V in human plasma and platelets

PB Tracy, LL Eide, EJ Bowie, KG Mann - 1982 - ashpublications.org
PB Tracy, LL Eide, EJ Bowie, KG Mann
1982ashpublications.org
Homogeneous, single-chain human factor V was used to develop a double antibody
competition radioimmunoassay to measure factor V concentrations in plasma and platelets.
Standard curves were constructed that allow for the detection of as little as 20 ng factor V/ml
of plasma. Normal factor V concentrations range from 4 to 14 micrograms/ml of plasma with
an average value of 7.0+/-2.0 micrograms/ml (n= 64). No correlation was observed between
antigen levels and age or sex. The radioimmunoassay data are consistent with factor V …
Abstract
Homogeneous, single-chain human factor V was used to develop a double antibody competition radioimmunoassay to measure factor V concentrations in plasma and platelets. Standard curves were constructed that allow for the detection of as little as 20 ng factor V/ml of plasma. Normal factor V concentrations range from 4 to 14 micrograms/ml of plasma with an average value of 7.0 +/- 2.0 micrograms/ml (n = 64). No correlation was observed between antigen levels and age or sex. The radioimmunoassay data are consistent with factor V clotting assays, providing freshly drawn plasma is used in the bioassay. Radioimmunoassay of washed platelets indicate that 0.63–1.93 microgram of factor V is present per 2.5 X 10(8) platelets (4612–14128 molecules of the factor V platelet). When normalized to individual hematocrits and platelet count, the data indicated that platelets contribute approximately 18%-25% of the factor V found in whole blood. In addition, two individuals with functionally deficient factor V were examined and found to be deficient in both antigen and activity.
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