Briefly, 2 lL of serum that had been diluted to
an adequate concentration with electrophoresis buffer
containing Triton X-100 (0.01-kg/L buffer) was applied on
the agarose gel (0.01 kg/L, SeaKem LE agarose, Marine
Colloids Division, FMC Corporation, Rockland, NY) plate
containing antiserum (125 lL of anti–apo A-I, 150 lL of
anti–apo A-IV, 150 AL of anti–apo B, or 300 AL of anti–apo
E per 9 mL of agarose gel solution) and subjected to
electrophoresis in 0.0148-mol/L barbital–0.075-mol/L Trisglycine
buffer (pH 8.8) containing Triton X-100 (1-g/L
buffer) at 8.4 V/cm at 14-168C for 3 hours for apo A-I and
apo E, or for 4 hours for apo A-IV and apo B.
Briefly, 2 lL of serum that had been diluted toan adequate concentration with electrophoresis buffercontaining Triton X-100 (0.01-kg/L buffer) was applied onthe agarose gel (0.01 kg/L, SeaKem LE agarose, MarineColloids Division, FMC Corporation, Rockland, NY) platecontaining antiserum (125 lL of anti–apo A-I, 150 lL ofanti–apo A-IV, 150 AL of anti–apo B, or 300 AL of anti–apoE per 9 mL of agarose gel solution) and subjected toelectrophoresis in 0.0148-mol/L barbital–0.075-mol/L Trisglycinebuffer (pH 8.8) containing Triton X-100 (1-g/Lbuffer) at 8.4 V/cm at 14-168C for 3 hours for apo A-I andapo E, or for 4 hours for apo A-IV and apo B.
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