1980
DOI: 10.1016/0022-1759(80)90091-5
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Determination of alternative pathway of complement activity in mouse serum using rabbit erythrocytes

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Cited by 45 publications
(17 citation statements)
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“…Spleen and liver were removed and immediately frozen in liquid nitrogen and stored at -70 "C. After clotting of the blood at 20°C for 1.5 h, serum was separated by centrifugation and subsquently stored at -70°C until use. Determination of the alternative C pathway activity was performed according to the procedure described by Van Dijk et al [18], using rabbit RBC as indicator cells. Alternative C pathway activity was expressed in AP50 U/ml, in which 1 AP50 U causes 50% lysis of the rabbit RBC.…”
Section: Depletion and Immunizationmentioning
confidence: 99%
“…Spleen and liver were removed and immediately frozen in liquid nitrogen and stored at -70 "C. After clotting of the blood at 20°C for 1.5 h, serum was separated by centrifugation and subsquently stored at -70°C until use. Determination of the alternative C pathway activity was performed according to the procedure described by Van Dijk et al [18], using rabbit RBC as indicator cells. Alternative C pathway activity was expressed in AP50 U/ml, in which 1 AP50 U causes 50% lysis of the rabbit RBC.…”
Section: Depletion and Immunizationmentioning
confidence: 99%
“…The basic principle for the activity determination of CP is based on the hemolysin pre-coated sheep erythrocytes which is hemolyzed by complement (Costabile, 2010). However, AP activity is analyzed with erythrocytes without hemolysin (Van Dijk, Rademaker, & Willers, 1980). The LP activity can also be detected by hemolytic assay (Kuipers, Aerts, Sjöholm, Harmsen, & van Dijk, 2002).…”
Section: Hemolytic Methodsmentioning
confidence: 99%
“…Serum C3 depletion was confirmed by alternative complement pathway activity as described previously [20].…”
Section: Cobra Venom Factor (Cof)mentioning
confidence: 99%