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Dystrophin anticorps

DMD Reactivité: Humain, Souris, Rat, Poulet WB, IHC (p) Hôte: Souris Monoclonal DYS-48 unconjugated
N° du produit ABIN1107040
  • Antigène Voir toutes Dystrophin (DMD) Anticorps
    Dystrophin (DMD)
    Reactivité
    • 57
    • 27
    • 26
    • 5
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat, Poulet
    Hôte
    • 40
    • 18
    Souris
    Clonalité
    • 30
    • 28
    Monoclonal
    Conjugué
    • 31
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Cet anticorp Dystrophin est non-conjugé
    Application
    • 22
    • 21
    • 14
    • 10
    • 6
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Specificité
    This antibody reacts to Dystrophin.
    Purification
    Affinity chromatography
    Immunogène
    Recombinant human dystrophin fragment.
    Clone
    DYS-48
    Isotype
    IgG2b
    Top Product
    Discover our top product DMD Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Reconstitution
    Restore with 1.2 % sodium acetate or neutral PBS
    Concentration
    0,1 mg/mL
    Buffer
    1.2 % sodium acetate, with 2 mg BSA and 0.01 mg sodium azide as preservative.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid repeated freezing and thawing.
    Stock
    -20 °C
    Stockage commentaire
    Prior to reconstitution store at -20 °C. Following reconstitution store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène
    Dystrophin (DMD)
    Autre désignation
    Dystrophin / DMD (DMD Produits)
    Synonymes
    anticorps DMD, anticorps Dmd, anticorps MGC83347, anticorps DKFZp459C1629, anticorps dmd, anticorps MGC79631, anticorps DKFZp468A1620, anticorps Dp71, anticorps cb664, anticorps zfDYS, anticorps im:6911785, anticorps zgc:110165, anticorps BMD, anticorps CMD3B, anticorps DXS142, anticorps DXS164, anticorps DXS206, anticorps DXS230, anticorps DXS239, anticorps DXS268, anticorps DXS269, anticorps DXS270, anticorps DXS272, anticorps DXSmh7, anticorps DXSmh9, anticorps Dp427, anticorps dys, anticorps mdx, anticorps pke, anticorps DNADMD1, anticorps RATDMD, anticorps CG17750, anticorps CG31175, anticorps CG34157, anticorps CG7240, anticorps CG7243, anticorps CG7344, anticorps DLP, anticorps DLP1, anticorps DLP186, anticorps DLP2, anticorps DLP3, anticorps DmDLP, anticorps DmDYS, anticorps Dmel\\CG34157, anticorps Dp117, anticorps Dp186, anticorps Dp205, anticorps GI3046716, anticorps IDLP, anticorps det, anticorps dmDLP, anticorps dmDp186, anticorps dmDys, anticorps dystrophin, anticorps dystrophin, gene 1 L homeolog, anticorps dystrophin, gene 1, anticorps dystrophin, muscular dystrophy, anticorps Dystrophin, anticorps DMD, anticorps LOC708073, anticorps dmd.1.L, anticorps LOC465557, anticorps dmd.1, anticorps dmd, anticorps Dmd, anticorps Dys
    Sujet
    Dystrophin(DMD) gene has 79 exons spanning at least 2,300 kb (2.3 Mb). The C terminus of the dystrophin protein is encoded by a highly conserved, alternatively spliced region of the gene. beta-dystroglycan binding activity is expressed by the dystrophin fragment spanning amino acids 3026-3345 containing the ZZ domain. DMD transcript is formed by at least 60 exons, the first half of the transcript is formed by a minimum of 33 exons spanning nearly 1000 kb, and the remaining portion has at least 27 exons that may spread over a similar distance. Dystrophin gene is expressed at a higher level in primary cultures of neuronal cells than in astro-glial cells derived from adult mouse brain.over expression of dystrophin prevents the development of the abnormal mechanical properties associated with dystrophic muscle without causing deleterious side effects.
    ID gène
    1756
    NCBI Accession
    NP_000100
    UniProt
    P11532
    Pathways
    Skeletal Muscle Fiber Development
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