Hop (Humulus lupulus L,) cones are used extensively in beer brewing to enha
nce flavor and impart bittering. Verifying hops cultivar identity has tradi
tionally been accomplished by morphological characteristics or a chemical a
nalysis of lupulin glands but these traits may vary according to environmen
tal influences. The objective of this research was to develop an AFLP (ampl
ified fragment length polymorphism) protocol for analyzing DNA extracted fr
om dried hop cones. The DNA was extracted from dried cones of six hop genot
ypes by a technique published for grapes (Vitis spp), The reagents, MseI pr
imers, and protocol were part of a commercially available kit, while the 6-
carboxyfluorescein-labeled EcoRI primers were purchased separately. Eleven
primer combinations amplified an average of 546.5 scorable fragments with a
n average of 49.7 fragments per primer combination. All genotypes were diff
erentiated with the primer combinations studied. Average genetic similarity
estimates ranged between 0.956 and 0.995 among the six hop genotypes studi
ed. This research provides the hops industry with a powerful technique to v
erify accurately hops cultivar identity and purity through an analysis of d
ried cone DNA.