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Dmd/Dmd蛋白Recombinant Rat Dystr

ophin (Dmd)重组蛋白/蛋白
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  • ¥2328 - 14796
  • CUSABIO已认证
  • CN
  • CSB-EP006963RA
  • 2025年07月15日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.

    • 保质期

      Generally, the shelf life of liquid form is 6 months at -20℃/-80℃. The shelf life of lyophilized form is 12 months at -20℃/-80℃.

    • 英文名

      Recombinant Rat Dystrophin (Dmd), partial

    • 库存

      200

    • 供应商

      武汉华美生物工程有限公司

    • 规格

      1mg/100μg/20μg

    规格:1mg产品价格:¥14796.0
    规格:100μg产品价格:¥4374.0
    规格:20μg产品价格:¥2328.0

    纯度:

    Greater than 90% as determined by SDS-PAGE.

    基因名:

    Dmd

    Uniprot No.:

    P11530

    别名:

    /

    种属:

    Rattus norvegicus (Rat)

    蛋白长度:

    Partial

    来源:

    E.coli

    分子量:

    35.0 kDa

    表达区域:

    1-240aa

    氨基酸序列:

    MLWWEEVEDCYEREDVQKKTFTKWINAQFSKFGKQHIDNLFSDLQDGKRLLDLLEGLTGQKLPKEKGSTRVHALNNVNKALQVLQKNNVDLVNIGSTDIVDGNHKLTLGLIWNIILHWQVKNVMKTIMAGLQQTNSEKILLSWVRESTRNYPQVNVLNFTSSWSDGLALNALIHSHRPDLFDWNSVVSQQSATQRLEHAFNIAKCQLGIEKLLDPEDVATTYPDKKSILMYITSLFQVLP

    蛋白标签:

    N-terminal 10xHis-tagged and C-terminal Myc-tagged

    产品提供形式:

    Liquid or Lyophilized powder

    缓冲液:

    If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, pH 8.0.

    货期:

    13-23 business days

    注意事项:

    Repeated freezing and thawing is not recommended. Store working aliquots at 4℃ for up to one week.

    功能:

    Anchors the extracellular matrix to the cytoskeleton via F-actin. Ligand for dystroglycan. Component of the dystrophin-associated glycoprotein complex which accumulates at the neuromuscular junction (NMJ) and at a variety of synapses in the peripheral and central nervous systems and has a structural function in stabilizing the sarcolemma. Also implicated in signaling events and synaptic transmission.

    内毒素:

    Not test.

    SDS-PAGE:

    (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.

    LC-MS Image Description/Western Blot:

    /

    Product types:

    Developed Protein

    Biological_Activity:

    /

    Research Areas:

    Signal Transduction

    Reconstitution:

    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.

    Reference:

    "Dystrophin splice variants are distinctly localized in the hippocampus." Hazai D., Halasy K., Mornet D., Hajos F., Jancsik V. Acta Biol Hung 57:141-146(2006) .

    Function:

    /

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    图标文献和实验
    该产品被引用文献
    "Dystrophin splice variants are distinctly localized in the hippocampus." Hazai D., Halasy K., Mornet D., Hajos F., Jancsik V. Acta Biol Hung 57:141-146(2006) .
    相关实验
    • DMD和BMD产前基因检测介绍

      杜氏进行性肌营养不良(Duchenne muscular dystrophy,DMD)和贝氏进行性肌营养不良(Becker muscular dystrophy,BMD)系X连锁隐性遗传病,是由于抗肌萎缩蛋白dystrophin)基因突变所致的肌源性损伤。基因突变的主要类型是基因片段缺失,在基因5‘端和3’端分别存在一个缺失高发区,尤其后者,以外显子51区域为高峰医学|教育网整理搜集,中国人病例近80 %的缺失突变发生在此区域。其中大范围(一个或数个外显子) 缺失型占60 % ,重复型

    • Denaturing Gradient Gel Electrophoresis (DGGE) for Mutation Detection in Duchenne Muscular Dystrophy (DMD)

      Duchenne muscular dystrophy (DMD) is an X-linked recessive neuromuscular disorder caused by mutations in the dystrophin gene at Xp21. Approximately two-thirds of the mutations are intragenic deletions of one or more of the 79 exons

    • Engineering Exon-Skipping Vectors Expressing U7 snRNA Constructs for Duchenne Muscular Dystrophy Gene Therapy

      Duchenne muscular dystrophy (DMD) is a fatal muscle wasting disorder caused by mutations in the dystrophin gene. In most cases, the open-reading frame is disrupted which results in the absence of a functional protein. Antisense-mediated exon

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    文献支持
    Dmd/Dmd蛋白Recombinant Rat Dystrophin (Dmd)重组蛋白/蛋白
    ¥2328 - 14796