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CHRND antibody (AA 22-245)

This anti-CHRND antibody is a Rabbit Polyclonal antibody detecting CHRND in WB. Suitable for Human.
Catalog No. ABIN6138596

Quick Overview for CHRND antibody (AA 22-245) (ABIN6138596)

Target

See all CHRND Antibodies
CHRND (Cholinergic Receptor, Nicotinic, delta (Muscle) (CHRND))

Reactivity

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  • 7
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This CHRND antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 22-245

    Sequence

    LNEEERLIRH LFQEKGYNKE LRPVAHKEES VDVALALTLS NLISLKEVEE TLTTNVWIEH GWTDNRLKWN AEEFGNISVL RLPPDMVWLP EIVLENNNDG SFQISYSCNV LVYHYGFVYW LPPAIFRSSC PISVTYFPFD WQNCSLKFSS LKYTAKEITL SLKQDAKENR TYPVEWIIID PEGFTENGEW EIVHRPARVN VDPRAPLDSP SRQDITFYLI IRRK

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 22-245 of human CHRND (NP_000742.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    CHRND (Cholinergic Receptor, Nicotinic, delta (Muscle) (CHRND))

    Alternative Name

    CHRND

    Background

    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.,CHRND,ACHRD,CMS2A,CMS3A,CMS3B,CMS3C,FCCMS,SCCMS,Neuroscience,Neurodegenerative Diseases,Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimer's Disease,CHRND

    Molecular Weight

    57 kDa/58 kDa

    Gene ID

    1144

    UniProt

    Q07001
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