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Recombinant Human CHRND Protei

n (N-His Tag), 重组人CHRND蛋白 (N端His标签)
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  • ¥1868
  • abinScience
  • France
  • HB513012
  • 2026年03月03日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.

    • 保质期

      1 year

    • 英文名

      Recombinant Human CHRND Protein, N-His

    • 库存

      999

    • 供应商

      abinScience

    • 规格

      100ug

    产品细节图片1

    Product nameRecombinant Human CHRND Protein, N-His
    Catalog No.HB513012
    FormLyophilized
    Storage bufferLyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.
    Purity>90% as determined by SDS-PAGE.
    ApplicationsELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
    Endotoxin levelPlease contact with the lab for this information.
    Expression systemE. coli
    AccessionQ07001
    ReconstitutionReconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
    Alternative NamesAcetylcholine receptor subunit delta; CHRND; ACHRD
    SpeciesHomo sapiens (Human)
    ShippingIn general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

    abinScience, founded in 2023 in Strasbourg, France, is committed to developing and producing high-quality life science reagents. Rooted in one of Europe’s leading hubs for scientific innovation, abinScience empowers global research through reliable, efficient experimental solutions. Guided by the vision of “Empowering Bioscience Discovery,” we support scientists worldwide in advancing the frontiers of bioscience.

     

    Technology and Innovation

    Relying on the global leading position in antibody and protein research and more than 20 years of industry experience of its parent company ProteoGenix since 2003...

     

    Product categories and application fields.

    Main products...
    Application field: Infectious disease research, Neuroscience, Immunology, Oncology

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    图标文献和实验
    该产品被引用文献
    • Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review., PMID:36835142
    • A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort., PMID:34602496
    • Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies., PMID:35302338
    • CHRND variant in a paternally inherited esophageal atresia and tracheoesophgageal fistula: Report of a case., PMID:38087897
    • Severe congenital myasthenic syndrome with novel variants in the CHRND gene., PMID:36370373
    • CHRND mutation causes a congenital myasthenic syndrome by impairing co-clustering of the acetylcholine receptor with rapsyn., PMID:16916845
    • Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients., PMID:38964204
    • Case Report: Early diagnosis of lethal multiple pterygium syndrome with micrognathia: Two novel mutations in the CHRND gene., PMID:36733345
    • Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients., PMID:18179903
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    文献支持
    Recombinant Human CHRND Protein (N-His Tag), 重组人CHRND蛋白 (N端His标签)
    ¥1868