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LOAG_05396 antibody (C-Term)

LOAG_05396 Reactivity: Human, Mouse, Rat ELISA, WB, ICC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN4888957
  • Target See all LOAG_05396 products
    LOAG_05396 (Acetylcholine Receptor Protein (LOAG_05396))
    Binding Specificity
    C-Term
    Reactivity
    Human, Mouse, Rat
    Host
    • 3
    Rabbit
    Clonality
    • 3
    Polyclonal
    Conjugate
    • 3
    This LOAG_05396 antibody is un-conjugated
    Application
    • 3
    • 3
    • 2
    • 1
    ELISA, Western Blotting (WB), Immunocytochemistry (ICC)
    Specificity
    Reacts with human CHRNB1 protein
    Cross-Reactivity
    Mouse (Murine), Rat (Rattus)
    Cross-Reactivity (Details)
    Cross reacts with protein from mouse, rat and other species due to sequence homology.
    Purification
    Purified (protein A)
    Immunogen
    Synthetic peptide derived from C-term domain of the human CHRNB1 protein.
  • Application Notes

    Working dilution: Optimal dilution should be determined by the end user.
    The following are guidelines only :
    ICC(1:100 - 1:500) WB(1:500 - 1:5000)

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Must be reconstituted in distilled water.
    Concentration
    1 mg/mL
    Buffer
    Tris 0,1M, glycine 0,1M, sucrose 2 %
    Storage
    4 °C/-20 °C
    Storage Comment
    Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.
    Expiry Date
    24 months
  • Target
    LOAG_05396 (Acetylcholine Receptor Protein (LOAG_05396))
    Alternative Name
    Acetylcholine receptor protein (LOAG_05396 Products)
    Synonyms
    acetylcholine receptor protein antibody, LOAG_05396 antibody
    Background
    Belongs to the ligand-gated ion channel family. Acetylcholine receptor subfamily. Beta-1/CHRNB1 sub-subfamily. Defects in CHRNB1 are a cause of congenital myasthenic syndrome slow-channel type (SCCMS) and congenital myasthenic syndrome with acetylcholine receptor deficiency (CMS-ACHRD).
    Gene ID
    1140
    UniProt
    P11230
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