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laburnum/peroxidase

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11 결과

[Populations of afferent neurons in the sensory ganglia detected using lectin from Laburnum anagyroides].

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The purpose of the present research was the study of afferent neuron subpopulations in vagal caudal ganglia and trigeminal ganglion of adult albino rats using a conjugate of fucose-specific Laburnum anagyroides lectin (LAL) with peroxidase. Histochemical preparations obtained were examined using

[Dissecting aneurysm of the aorta: histochemical study using a set of lectins with different carbohydrate specificity].

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By means of lectin-peroxidase technique histotopography of receptor sites for Ricinus communis agglutinin (RCA), peanut agglutinin (PA), soybean agglutinin (SA), Sophora japonica lectin (SJL), wheat germ agglutinin (WGA), Laburnum anagyroides lectin (LAL), Lotus tetragonolobus lectin (LTL) and

[Lectin receptors in the salivary glands of the rat during postnatal ontogenesis].

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Distribution of lectin-binding sites in rat submandibular and sublingual salivary glands during postnatal development has been investigated. Lectin preparations include con A, lentin lectin, castor beans agglutinin, peanut, soybean and Sophora japonica agglutinins, wheat germ agglutinin and lectin
Histotopography of lectin receptor sites in adult mice ovary, oviduct, uterus, testis and epididymis has been investigated on light-optic level by means of lectin-peroxidase technique. Paraffin sections are treated with peanut agglutinin (PNA), soybean agglutinin (SBA), wheat germ agglutinin (WGA)

Lectinocytochemical detection of apoptotic murine leukemia L1210 cells.

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BACKGROUND Various cytomorphologic and biochemical markers of apoptosis are found in different compartments (plasma membrane, cytoplasm, nucleus, and mitochondria) of target cells. Although the plasma membrane is an easily accessible cellular compartment, relatively little is known about its changes

[Lectin-binding proteins of plasma membranes of a human trophoblast].

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Spectra of lectin-binding proteins of the human trophoblast were studied by the method affinity blotting using a set of loctins conjugated with peroxidase. The set included lectins Lens culinaris (LcL), Canavalia ensiformis (Con A), Ricinus communis (RCA 1), Arachis hypogaea (PNA), Triticum vulgaris

[Lectin histochemistry of human placenta in the normal state and in uterine inertia].

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The lectin-peroxidase technique has been used. The peanut lectin is able to label selectively Kashchenko--Hofbauer cells, villi of the chorion; the soya lectin--decidual cells in the maternal part of the placenta. Prolonged labour development is connected with disappearance of Kashchenko--Hofbauer

[Effect of thyroid hormones on the histotopography of lectin receptors in the rat salivary gland].

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Using lectin-peroxidase technique, the influence of hypo- and hyperthyroidism on histotopography of glycoconjugates has been investigated in rat submandibular gland. The following lectins were used: peanut agglutinin (PNA), wheat germ agglutinin (WGA), Laburnum anagyroides lectin (LAL) and

[Lectin binding by structures of the submandibular gland of the rat during postnatal ontogenesis in the presence of thyroid pathology].

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Redistribution of lectin receptor sites in rat submandibular gland under hypo- and hyperthyroidism has been investigated using lectin-peroxidase technique. Lectin preparation include con A, peanut agglutinin (PNA), wheat germ agglutinin (WGA) and fucose-specific lectin from Laburnum anagyroides bark

Lectin receptor sites during postnatal osteogenesis in guinea pigs.

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BACKGROUND Osteoporosis and its complications have become widespread, affecting large portions of the world's population. More advanced information is needed on these pathologies to expand the possibilities for pathogenetic therapy. OBJECTIVE Lectin histochemistry methods offer new insights into the
BACKGROUND Despite the widespread use of roots of Cassia sieberiana in managing several health conditions including gastric ulcer disease, there is little scientific data to support the rational phytotherapeutics as an anti-ulcer agent. This paper reports an evaluation of the in vivo anti-oxidant
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