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<meta name="Description" content="There was a significant difference in terms of lectin content in various organs and different species of the genus Geranium, particularly in the aerial parts of G. sanguineum L. (22) RHA titer values are 7 positions lower than those of rhizomes (29); lectin content values in the aerial parts of G. macrorrhizum L. (25) less than 2 positions with those of rhizomes (27), the corresponding proportions of the values observed in G. sibiricum L. In G. robertianum L. grass, lectins were absent and only found in small amounts in the rhizomes. It is interesting to note that lectin content in the studied plant material increases during seasonal growth (from the beginning of vegetation to plant flowering). This dependence is observed in all studied species of the genus Geranium L. It should be noted that the highest assay values of lectin content were observed in roots of the species Geranium sanguineum L. (RHA titer - 29), G. macrorrhizum L. (RHA titer - 29) and G. sibiricum L. (RHA titer - 27)." />
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<title>Research on Quantitative Content of Lectins in Plants of the Geranium L. Genus</title>
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<h2 align="center" class="style6">Volume <span class="style11">2</span>, Issue 6</h2>
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<h6 align="center" class="style1">Research on Quantitative Content of Lectins in Plants of the <em>Geranium</em> L. Genus </h6>
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<p><span class="style10">Authors: </span><span class="style5">Lyubov Rybak <sup>1</sup>*, Galina Rudik<sup>2</sup><br />
1. State Drug Quality Control Laboratory of Institute of Pharmacology and Toxicology, National Academy of Medical Sciences of Ukraine, Kyiv, Ukraine</span></p>
<p class="style5">2. "Botanical Garden" Research Laboratory of the "Institute of Biology" of the Scientific and Educational Center at Kyiv National Taras Shevchenko University, Kyiv, Ukraine</p>
<p><span class="style10">Abstract:</span> <span class="style5">Results of a comparative study of the quantitative content of lectins in four plant species of the <em>Geranium</em> L. genus of flora of Ukraine. Quantitative lectin content was determined by the reaction of hemagglutination of human erythrocytes.</span></p>
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