| Literature DB >> 27720768 |
Samine Rahmatpour1, Amjad Hayat Khan2, Rasoul Nasiri Kalmarzi3, Masoumeh Rajabibazl4, Gholamreza Tavoosidana5, Elahe Motevaseli5, Nosratollah Zarghami6, Esmaeil Sadroddiny7.
Abstract
In vivo and in vitro tests are the two major ways of identifying the triggering allergens in sensitized individuals with allergic symptoms. Both methods are equally significant in terms of sensitivity and specificity. However, in certain circumstances, in vitro methods are highly preferred because they circumvent the use of sensitizing drugs in patients. In current study, we described a highly sensitive immuno-PCR (iPCR) assay for serum IgE specific to Bermuda allergens. Using oligonucleotide-labelled antibody, we used iPCR for the sensitive detection of serum IgE. The nucleotide sequence was amplified using conventional PCR and the bands were visualized on 2.5% agarose gel. Results demonstrated a 100-fold enhancement in sensitivity of iPCR over commercially available enzyme-linked immunosorbent assay (ELISA) kit. Our iPCR method was highly sensitive for Bermuda-specific serum IgE and could be beneficial in allergy clinics.Entities:
Keywords: Detecting type I allergy; Detection of serum IgE; Diagnosing allergy; Immuno-PCR; In vitro IgE tests
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Year: 2016 PMID: 27720768 DOI: 10.1016/j.mcp.2016.10.002
Source DB: PubMed Journal: Mol Cell Probes ISSN: 0890-8508 Impact factor: 2.365