1 Ocak 2016 Dergi makalesi Açık Erişim

Bahadir, Elif Burcu; Sezginturk, Mustafa Kemal

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  "@id": 58545, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Namik Kemal Univ, Sci & Technol Res Ctr, Tekirdag, Turkey", 
      "name": "Bahadir, Elif Burcu"
    }, 
    {
      "@type": "Person", 
      "affiliation": "Namik Kemal Univ, Dept Chem, Fac Sci, Div Biochem, Tekirdag, Turkey", 
      "name": "Sezginturk, Mustafa Kemal"
    }
  ], 
  "datePublished": "2016-01-01", 
  "description": "Lateral flow assays (LFAs) have attracted interest due to their friendly user formats, short assay times, little interferences, low costs, and being easy by operated by non-specialized personnel. This technique is based on biochemical interaction of antigen-antibody or probe DNA-target DNA hybridization. A lateral flow assay (LFA) is composed of four parts: a sample pad, which is the area on which sample is dropped; conjugate pad, on which labeled tags combined with biorecognition elements; reaction membrane containing test line and control line for target DNA-probe DNA hybridization or antigen-antibody interaction; and absorbent pad, which reserves waste. For the construction of LFAs gold nanoparticles, colored latex beads, carbon nanoparticles, quantum dots, and enzymes are used as a label for increasing the sensitivity. In this work, the principle of LFAs, biorecognition elements, analytical performances, limits of detection (LODs), linear ranges of developed LFAs in different fields are summarized. Future perspectives in this area are also discussed. (C) 2016 Elsevier B.V. All rights reserved.", 
  "headline": "Lateral flow assays: Principles, designs and labels", 
  "identifier": 58545, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Lateral flow assays: Principles, designs and labels", 
  "url": "https://aperta.ulakbim.gov.tr/record/58545"
}