Sheep Washed Pooled Cells, Sheep WPCs, Sheep Red Blood Cells, Sheep RBCs, erythrocytes
Buffer:
0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Source:
Sheep
Form:
Liquid
Application Notes:
Complement titration, adsorption procedures, HA assays and for the preparation of stroma as particulate reagents.
Delta9-THC suppresses the secondary plaque-forming cell response via CB2 receptors. A dose titration of THC, with or without a CB1 or CB2 antagonist, was carried out using spleen cells in a secondary PFC assay. Each experiment was repeated 3 times, with triplicate wells for each dose. *p< 0.05 vs. THC alone. Values for vehicle or antagonists alone are not significantly different from 1.0. Sheep red blood cells (p/n R405-0050.) Fig. 2. PMID: 17640739.
WT and PPARalphaKO mice were immunized on the 11th day of dosing (0, 7.5, or 30mg PFOA/kg/day) by intravenous injection of 4.0*107 sheep red blood cells (SRBC, p/n R405-0050) in 0.2ml of sterile saline.T-cell-dependent (TDAR) or T-cell-independent (TIAR) IgM antibody responses. Responses of mice exposed to PFOA via drinking water for 15 days, evaluated in sera collected 1 day (TDAR) or 2 days (TIAR) after exposure ended. Data represent meanSD. (a) The TDAR of wild-type C57BL/6-Tac (WT) or PPARalphaknockout (KO) B6.129S4-Ppartm1GonzN12mice (n=6/strain/dose). The TDAR did not differ between WT or PPARalphaKO mice at any dose. (b) The TIAR of C57BL/6N mice (n=8/dose). *Statistical (p<0.05) difference between treated group and corresponding 0mg PFOA/kg group. Figure 3. PMID: 25594567.
Krogh plot: Concentration-dependent lysis of sheep red blood cells (SRBCs) [p/n R405-0050] by alligator and human serum. Serum samples were incubated with 1% SRBCs in a 1.0 mL reaction for 30 min at ambient temperature. The optical density of each sample was determined at 525 nm. The results are expressed as the percentage maximum lysis and represent the means +/-standard deviations for four determinations. Fig. 1. PMID: 15921941.
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