Identifying Crabapple Cultivars by Isozymes

dc.contributor.authorRobert D. Marquard
dc.contributor.authorCharlotte R. Chan
dc.date.accessioned2014-07-31T04:38:48Z
dc.date.available2014-07-31T04:38:48Z
dc.date.issued1995
dc.description.abstractForty-flve crabapple (Malus spp.) cultivars were evaluated for 16 isozyme systems by starch gel electrophoresis. Of the 16 systems evaluated, 6 were useful in separating among cultivars. Enzyme systems used to distinguish among the cultivars included alcohol dehydrogenase, aspartate aminotransferase, malate dehydrogenase, 6-phosphogluconate dehydrogenase, phosphoglucoisomerase, and shikimate dehydrogenase. Each enzyme system produced one well-resolved polymorphic region except for 6-phosphogluconate dehydrogenase, which produced two. Most crabapple selections could be identified when all six enzymes were evaluated. Alcohol dehydrogenase had the most diagnostic banding patterns useful for cultlvar Identification.en_US
dc.identifier.citationJ. Amer. Soc. Hort. Sci. 120(5): 706-709, 1995en_US
dc.identifier.urihttp://hdl.handle.net/123456789/4444
dc.language.isoenen_US
dc.subjectmalusen_US
dc.subjectisoenzymeen_US
dc.subjectstarch gel electrophoresisen_US
dc.titleIdentifying Crabapple Cultivars by Isozymesen_US
dc.typeArticleen_US

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
rp 1141.pdf
Size:
311.99 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description:

Collections