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Myosin 9 anticorps (C-Term)

MYH9 Reactivité: Humain, Souris WB Hôte: Lapin Polyclonal RB38850 unconjugated
N° du produit ABIN1536807
  • Antigène Voir toutes Myosin 9 (MYH9) Anticorps
    Myosin 9 (MYH9)
    Épitope
    • 7
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1840-1867, C-Term
    Reactivité
    • 57
    • 13
    • 11
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 44
    • 11
    • 2
    • 1
    • 1
    Lapin
    Clonalité
    • 44
    • 15
    Polyclonal
    Conjugué
    • 39
    • 5
    • 5
    • 5
    • 2
    • 2
    • 1
    Cet anticorp Myosin 9 est non-conjugé
    Application
    • 45
    • 36
    • 16
    • 14
    • 11
    • 9
    • 8
    • 6
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogène
    This MYH9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1840-1867 amino acids from the C-terminal region of human MYH9.
    Clone
    RB38850
    Isotype
    Ig Fraction
    Top Product
    Discover our top product MYH9 Anticorps primaire
  • Indications d'application
    WB: 1:2000. WB: 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    MYH9 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    Date de péremption
    6 months
  • Antigène
    Myosin 9 (MYH9)
    Autre désignation
    MYH9 (MYH9 Produits)
    Sujet
    This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
    Poids moléculaire
    226532
    ID gène
    4627
    NCBI Accession
    NP_002464
    UniProt
    P35579
    Pathways
    Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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