A MODIFIED SODIUM DODECYL SULFATE-AGAROSE GEL IMMUNOBLOTTING METHOD FOR APOLIPOPROTEIN(A) PHENOTYPING USING ALKALINE PHOSPHATASE-LINKED CHEMILUMINESCENT DETECTION
Rwc. Pang et al., A MODIFIED SODIUM DODECYL SULFATE-AGAROSE GEL IMMUNOBLOTTING METHOD FOR APOLIPOPROTEIN(A) PHENOTYPING USING ALKALINE PHOSPHATASE-LINKED CHEMILUMINESCENT DETECTION, Annals of clinical biochemistry, 34, 1997, pp. 314-316
Apolipoprotein(a) [apo(a)] is a highly polymorphic plasminogen-like gl
ycoprotein and is the distinctive constituent of lipoprotein(a) [Lp(a)
]. The size heterogeneity of apo(a) is due to differences in the numbe
r of kringle IV (K-IV) encoding repeats in the apo(a) gene and this is
responsible for the size polymorphism in the expressed proteins (phen
otypes).(1) Apo(a) genomic DNA size polymorphism has been demonstrated
by using pulsed field gel electrophoresis (PFGE) followed by Southern
blot hybridized with specific probes and this has shown that the numb
er of K-IV repeats ranges between 12 and 51. We describe a simplified
sodium dodecyl sulphate (SDS)-agarose gel electrophoresis (AGE) method
for apo(a) phenotyping using alkaline phosphatase-linked chemilumines
cent detection. Apo(a) isoforms were designated according to the numbe
r of K-IV repeats.