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CHRND antibody (AA 22-245)

CHRND Reactivity: Human WB, ELISA, FACS Host: Mouse Monoclonal 1H1F9 unconjugated
Catalog No. ABIN5611361
  • Target See all CHRND Antibodies
    CHRND (Cholinergic Receptor, Nicotinic, delta (Muscle) (CHRND))
    Binding Specificity
    • 7
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 22-245
    Reactivity
    • 29
    • 7
    • 7
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    Human
    Host
    • 28
    • 1
    Mouse
    Clonality
    • 28
    • 1
    Monoclonal
    Conjugate
    • 21
    • 2
    • 2
    • 2
    • 1
    • 1
    This CHRND antibody is un-conjugated
    Application
    • 23
    • 15
    • 9
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Flow Cytometry (FACS)
    Purpose
    CHRND Antibody
    Purification
    Purified antibody
    Immunogen
    Purified recombinant fragment of human CHRND (AA: 22-245) expressed in E. Coli.
    Clone
    1H1F9
    Isotype
    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified antibody in PBS with 0.05 % sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Storage Comment
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target
    CHRND (Cholinergic Receptor, Nicotinic, delta (Muscle) (CHRND))
    Alternative Name
    CHRND (CHRND Products)
    Background

    Description: The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene.

    Aliases: ACHRD, CMS2A, CMS3A, CMS3B, CMS3C, FCCMS, SCCMS

    Molecular Weight
    58.8kDa
    Gene ID
    1144
    HGNC
    1144
    UniProt
    Q07001
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