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OmpA

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  • $255 - 1350
  • prospecbio
  • PRO-571
  • 以色列
  • 2025年07月14日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      大量

    • 英文名

      Outer Membrane Protein-A Bacterial Recombinant

    • 保质期

      1年

    • 供应商

      上海沪震实业有限公司

    • 保存条件

      -20°C

    • 规格

      100μg/200μg/1mg

    OmpA

    CATALOGUE NUMBER

    PRO-571

    SYNONYMS

    Outer Membrane Protein-A, OmpA.

    INTRODUCTION

    The OmpA protein is one of the main outer-membrane proteins of a large array of Gram-negative bacteria such as A.salmonicida, Shigella dysenteriae and E.coli.OmpA’s major physiological functions include maintenance of the structural integrity and morphology of the cells and porin activity, as well as a role in conjugation and bacteriophage binding.Achromogenic atypical Aeromonas salmonicida is the causative agent of goldfish ulcer disease.Virulence of this bacterium is associated with the production of a paracrystalline outer membrane A-layer protein.The species specific structural gene for the monomeric form of A-protein was cloned into a pET-3d plasmid in order to express and produce a recombinant form of the protein in E.coli BL21(DE3). The induced protein was isolated from inclusion bodies by a simple solubilization-renaturation procedure and purified by ion exchange chromatography on Q-Sepharose to over 95% pure monomeric protein.Recombinant A-protein was compared by biochemical, immunological and molecular methods with the A-protein isolated from atypical A.salmonicida bacterial cells by the glycine and the membrane extraction methods.

    DESCRIPTION

    The recombinant form was found to be undistinguishable from the wild type when examined by SDS-PAGE and gel filtration chromatography yielding a 48 kDa monomeric protein. The immunological similarity of the protein samples was demonstrated by employing polyclonal and monoclonal antibodies in ELISA and Western Blot techniques. All forms of A-protein were found to activate the secretion of tumour necrosis factor alpha from murine macrophage. For ref see Maurice et al. (1999) Protein Expression and Purification 16, 396-404.
    The OmpA is purified by proprietary chromatographic techniques.

    SOURCE

    Escherichia Coli.

    PHYSICAL APPEARANCE

    Sterile Filtered White lyophilized (freeze-dried) powder.

    FORMULATION

    The OmpA protein was lyophilized from a concentrated (1mg/ml) solution with 0.02% NaHCO3.

    SOLUBILITY

    It is recommended to reconstitute the lyophilized OmpA in sterile 0.4% NaHCO3, not less than 100µg/ml, which can then be further diluted to other aqueous solutions.

    STABILITY

    Lyophilized Bacterial Outer Membrane Protein-A although stable at room temperature for 3 weeks, should be stored desiccated below -18°C. Upon C between 2-7 days and for future use reconstituted OmpA should be stored at 4 below -18°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). 
    Please avoid freeze-thaw cycles.

    PURITY

    Greater than 98.0% as determined by:
    (a) Analysis by SEC-HPLC.
    (b) Analysis by SDS-PAGE.

    AMINO ACID SEQUENCE

    mdvvispndn tfvttslasv tkqpvldfst aqqnltlnfs evgdlknngf ivleiqgegq fndaeirqwl sngfwrrpft gllvnpndhg nfansgevnd vrkffkiisd gtqltivhti dsngkrlrla lasdveetin fadaevelkl nlanqafklt sgsqgtvalt agalwnasyt adpvatkplf klgklfqlsl tnagkatalv segflklnig danisatdfa itnvttnqti qrdkvnltlt gdvsafkkda ngnlvnkaga sigwkaaadg qsatavlgag nmaggvqnal aafgtlyvaa dntvpvpavn fnvkaeiqgd sqatynyfkd eladlfiltr dgmkfdtitt gttsanlihi rdvsnilpte ggkifvtite yadhaangrg egtvlvtrka lsvtlpsgga vtlkpadvaa dvgasitagr qarlvfevet nqgevavkks naegvdiqng trgtaplvdf tl.

    BIOLOGICAL ACTIVITY

    The interaction of bacterial and recombinant A-layer protein with murine macrophages was directed at determining the effect of A-protein on intracellular events that occur in primed macrophages. This was accomplished by measuring the cytotoxic product produced by peritoneal macrophages when exposed to A-protein coated latex beads. Thioglycolate elicited macrophages exhibited a low level of activation (18% cytotoxicity) that was significantly increased (48% cytotoxicity) in the presence of latex beads. Coating of the latex beads with each of the three A-protein products resulted in an increase of cytoxicity (mean +/- SEM) from 48% to 91%.

    USAGE

    ProSpec's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.

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    图标文献和实验
    相关实验
    • 膜蛋白纯化攻略分享

      柱体积 30%。 分子筛 膜蛋白的纯化流程中,分子筛是理想化的最终步骤。不仅可以去除聚集体以及与目的蛋白大小不同的杂质,还可以进行缓冲液更换。这些因素往往能够决定后续的结构测定是否顺利。 推荐使用高分辨率分子筛大体积预装柱 Superdex 200 Increase 10/300 GL 和 Superose 6 Increase 10/300 GL。其最大上样量可达 500μL。   案例分析 外膜蛋白 A (Outer membrane protein A, OmpA) 是革兰氏阴性菌外膜蛋白质的主要

    • 最难搞的膜蛋白纯化攻略来了!

      500µl。 案例分析 外膜蛋白 A(Outer membrane protein A, OmpA)是革兰氏阴性菌外膜蛋白质的主要组分,也是一个关键的毒性因子,且与细菌生物膜合成、真核细胞感染、抗生素抗性和免疫调节息息相关。因此可作为一个潜在的药物靶点。 以下是从大肠杆菌中纯化非标签膜蛋白 OmpA 亚单位的流程。 首先使用合适的去垢剂 C8E4,把 OmpA 膜蛋白溶解出来; 然后使用阴离子交换层析柱 RESOURCE Q 1 ml 进行初步纯化,收集目标

    • 【求助】BAC文库应用

      -1,pBADHis, pBADHislacZ,pLLP ompA, pINIIIompA, pMBP-P ,pMBP-C 共表达质粒:pCDFduet-1 以及pCDNA3.1,pEGFP-N2等 大肠杆菌Rosetta(DE3),Rasettagame(DE3),Top10F', BL21(DE3)plySS 等 酵母表达质粒: pPICZαA, pGAPZαA, 酵母细胞 KM71, X33 yingzi

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