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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Identification of myosin heavy chain isoforms in porcine longissimus dorsi muscle by electrophoresis and mass spectrometry
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Identification of myosin heavy chain isoforms in porcine longissimus dorsi muscle by electrophoresis and mass spectrometry

机译:电泳和质谱鉴定猪背最长肌肌球蛋白重链同工型

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摘要

Myosin heavy chain (MHC) isoforms have been considered as makers for muscle fiber types in relation to meat quality, whereas MHC isoforms in porcine skeletal muscle have not been fully identified. The improved technique of SDS-PAGE and 2DE were used to separate porcine MHC isoforms. Western blotting with monoclonal antibodies including BA-F8 (anti-MHC slow/I), SC-71 (anti-MHC 2a and 2x), 10F5 (anti-MHC 2b), and BF-35 (anti-MHC slow/I and 2a) and MS were used to confirm MHC migration rate and identify MHC isoforms from separated bands and spots. Up to 45% w/v of glycerol, 8% w/v of acrylamide content, and 25 h of electrophoretic time at 70 V allowed a clear separation of MHC isoforms. Major MHC isoforms such as slow, 2a, 2x, and 2b were clearly separated by SDS-PAGE. A total of 23 MHC spots were separated and identified by 2DE and MS. Therefore, four MHC isoforms such as slow/I, 2a, 2x, and 2b could be identified by the improved SDS-PAGEtechnique, 2DE and MS. Therefore, these techniques allow more accurate and accessible analysis in muscle fiber typing and in relationship between MHC isoforms, muscle fiber characteristics, and pork quality.
机译:肌球蛋白重链(MHC)同工型被认为是与肉质相关的肌肉纤维类型的制造者,而猪骨骼肌中的MHC同工型尚未完全鉴定。 SDS-PAGE和2DE的改进技术用于分离猪MHC同工型。用单克隆抗体包括BA-F8(抗MHC慢/ I),SC-71(抗MHC 2a和2x),10F5(抗MHC 2b)和BF-35(抗MHC慢/ I和2a)和MS用于确认MHC迁移速率并从分离的条带和斑点中鉴定MHC亚型。高达45%w / v的甘油,8%w / v的丙烯酰胺含量和70 V的25 h电泳时间可以清楚地分离MHC亚型。通过SDS-PAGE可以清楚地分离出MHC的主要同工型,例如slow,2a,2x和2b。通过2DE和MS分离并鉴定了总共23个MHC斑点。因此,可以通过改进的SDS-PAGE技术,2DE和MS鉴定出四种MHC亚型,例如slow / I,2a,2x和2b。因此,这些技术可以对肌纤维类型以及MHC同工型,肌纤维特性和猪肉品质之间的关系进行更准确,更容易的分析。

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