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Production of antisera to synthetic decapeptide of the Cooh-Terminus of rat glut2

机译:对大鼠glut2 Cooh-Termin合成十肽产生抗血清

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In the present study, the production of an anti-GLUT 2 antibody is reported. The antibody (S-5096) was raised in New Zealand rabbits immunized with an immunogen prepared by cross-linking the synthetic peptide and a carrier protein. A COOH-terminal decapeptide of rat GLUT 2 predicted sequence was synthesized and coupled to keyhole limpet hemocyanin, using the glutaraldehyde method. Subcellular membrane fractions were prepared from renal cortex (C) and medulla (M), and subjected to Western blotting analysis using the antiserum in a 1:200 dilution and, subsequently, [125I]protein A. As the results showed, the S-5096 anti-serum showed clear blots in kidney samples, stronger in cortex than in medulla as expected, whereas white adipose tissue and heart samples did not show any immunoreactivity. In addition, immunoblots were detected in samples prepared from duodenum and jejunum, as well as from isolated pancreatic B cells. In conclusion, the results clearly show that an anti-Glut 2 antibody, efficient enough to detect the rat protein by Western blotting analysis, was obtained.
机译:在本研究中,报道了抗GLUT 2抗体的产生。抗体(S-5096)在新西兰兔中产生,该兔用通过将合成肽和载体蛋白交联制备的免疫原进行免疫。合成了大鼠GLUT 2预测序列的COOH末端十肽,并使用戊二醛法将其偶联到匙孔血蓝蛋白上。从肾皮质(C)和延髓(M)制备亚细胞膜级分,并使用1:200稀释的抗血清和[125I]蛋白A进行蛋白质印迹分析。结果表明,S- 5096抗血清在肾脏样品中显示出清晰的污点,在皮质中比在髓样中强,如预期的那样,而白色脂肪组织和心脏样品未显示任何免疫反应性。此外,在从十二指肠和空肠以及分离的胰腺B细胞制备的样品中检测到免疫印迹。总之,结果清楚地表明,获得了足以通过Western印迹分析检测大鼠蛋白质的抗Glut 2抗体。

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