| Literature DB >> 28293949 |
Erica Brunelle1, Anh Minh Le1, Crystal Huynh1, Kelly Wingfield1, Lenka Halámková1, Juliana Agudelo1, Jan Halámek1.
Abstract
The Bradford reagent, comprised of the Coomassie Brilliant Blue G-250 dye, methanol, and phosphoric acid, has been traditionally used for quantifying proteins. Use of this reagent in the Bradford assay relies on the binding of the Coomassie Blue G-250 dye to proteins. However, the ability of the dye to react with a small group of amino acids (arginine, histidine, lysine, phenylalanine, tyrosine, and tryptophan) makes it a viable chemical assay for fingerprint analysis in order to identify the biological sex of the fingerprint originator. It is recognized that the identification of biological sex has been readily accomplished using two other methods; however, both of those systems are reliant upon a large group of amino acids, 23 to be precise. The Bradford assay, described here, was developed specifically to aid in the transition from targeting large groups of amino acids, as demonstrated in the previous studies, to targeting only a single amino acid without compromising the intensity of the response and/or the ability to differentiate between two attributes. In this work, we aim to differentiate between female fingerprints and male fingerprints.Entities:
Year: 2017 PMID: 28293949 DOI: 10.1021/acs.analchem.7b00510
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986