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It is well established that the ingestion of cereal prolamins, such as gluten, causes the characteristic symptoms of celiac disease (CD) in people predisposed to it. DNA-based PCR method provides new ways to detect gluten in processed foodstuffs, such as bread. The aim of this work was to adapt a new primer pair combination and to initiate a carefully elaborated PCR methodology to experiment with DNA-based analysis. At first, the purity of cleaned DNA was verified using B49317 and A49855 chloroplast DNA primer pair. Then TR01/2 wheat specific PCR primer pair was used for checking the origin of the DNA, and P1/2 microsatellite (SSR) adapted primer pair for detecting allergen (gluten) specific residues. Method optimisation was achieved with cereal flour samples, then bread and dry pasta products from wheat were used, which were analysed as heat-treated samples with three primer pairs. The gluten specific primer pair was tested on cross-reactive cereals such as rye, barley, triticale and on some questionable cereals, such as oat, and pseudo-cereals, e.g. buck wheat and amaranth.

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Agar, G., Yildirim, N., Ercisli, S., Ergul, A. & Yuksel, C. (2012): Determination of genetic diversity of Vitis vinifera cv. Kabarcik populations from the Coruh Valley using SSR markers

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Chakravarthi, B.K. & Naravaneni, R. (2006): SSR marker based DNA finger-printing and diversity study in rice ( Oryza sativa L.). Afr. J. Biotechnol. , 5 , 684–688. Naravaneni R SSR marker

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the corresponding change of Eqs. 15 – 16 : (18) (19) The set of values of rate constants calculated for the two chosen reaction models are shown in Table 3 . The value “opt” refers to the minimal value of SSR. The values of “min” and “max

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