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Recombinant Human Jagged-1/JAG

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  • ¥1200 - 3520
  • 近岸蛋白(Novoprotein)已认证
  • 中国
  • CB95
  • 2026年02月19日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 英文名

      Recombinant Human Jagged-1/JAG1

    • 规格

      10ug/50ug/500ug/1mg

    规格:10ug产品价格:¥1200.0
    规格:50ug产品价格:¥3520.0
    规格:500ug产品价格:询价
    规格:1mg产品价格:询价

    Recombinant Human Jagged-1/JAG1 (CB95)

     

    产品说明(Description)

    Recombinant Human jagged-1 is produced by our Mammalian expression system and the target gene encoding Gln34-Ser1046 is expressed with a Fc tag at the C-terminus. 

    Accession #: P78504

    Known as: Protein jagged-1 I; Jagged-1; JAGL1; HJ1; JAG1 and CD339

     

    制剂(Formulation)

    Lyophilized from a 0.2 μm filtered solution of PBS, pH7.4.

     

    质量控制(Quality Control) 

     

    Purity:            Greater than 90% as determined by reducing SDS-PAGE.    

    Endotoxin:    Less than 0.1 ng/ug (1 EU/ug) as determined by LAL test.

     

    复溶(Reconstitution)

    Always centrifuge tubes before opening. Do not mix by vortex or pipetting.
    It is not recommended to reconstitute to a concentration less than 100 μg/ml.
    Dissolve the lyophilized protein in distilled water.
    Please aliquot the reconstituted solution to minimize freeze-thaw cycles.    

     

    保存(Storage)

    Lyophilized protein should be stored at < -20°C, though stable at room temperature for 3 weeks.Reconstituted protein solution can be stored at 4-7°C for 2-7 days.Aliquots of reconstituted samples are stable at < -20°C for 3 months.    

     

    背景(Background)

    Protein jagged-1 I, also known as Jagged-1, JAGL1, HJ1, JAG1 and CD339, is a single-pass type I membrane protein. JAG1 contains one DSL domain and sixteen EGF-like domain. JAG1 acts as a ligand for multiple Notch receptors and is involved in the mediation of Notch signaling. JAG1 may participate in early and late stages of mammalian cardiovascular development, JAG1 inhibits myoblast differentiation and enhances fibroblast growth factor-induced angiogenesis. Defects in JAG1 are the cause of Alagille syndrome type 1, which is autosomal dominant multisystem disorder defined clinically by hepatic bile duct paucity and cholestasis in association with cardiac, skeletal, and ophthalmologic manifestations.

     

    电泳(SDS-PAGE)

     

    FOR RESEARCH USE ONLY

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