PMC:5985359 / 7713-8289 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/5985359","sourcedb":"PMC","sourceid":"5985359","source_url":"https://www.ncbi.nlm.nih.gov/pmc/5985359","text":"Genomic DNA was extracted from whole blood using conventional methodologies. A short tandem repeat (STR) assay was performed to genotype the CTG18.1 allele, in accordance with methods previously published by Wieben et al.9 In brief, genomic DNA was amplified using a 5′FAM conjugated primer (5′-CAGATGAGTTTGGTGTAAGAT-3′) and an unlabeled reverse primer (5′-ACAAGCAGAAAGGGGGCTGCAA-3′). Post PCR product separation was performed on the ABI 3730 Electrophoresis 96 capillary DNA analyzer (Applied Biosystems). Data analysis was performed using GeneMarker software (SoftGenetics).","tracks":[{"project":"2_test","denotations":[{"id":"29526280-23185296-2044772","span":{"begin":221,"end":222},"obj":"23185296"}],"attributes":[{"subj":"29526280-23185296-2044772","pred":"source","obj":"2_test"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"2_test","color":"#e993ec","default":true}]}]}}