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RCN2 antibody

RCN2 Reactivity: Human, Mouse, Rat WB, IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7118413
  • Target See all RCN2 Antibodies
    RCN2 (Reticulocalbin 2, EF-Hand Calcium Binding Domain (RCN2))
    Reactivity
    Human, Mouse, Rat
    Host
    • 9
    • 4
    Rabbit
    Clonality
    • 11
    • 2
    Polyclonal
    Conjugate
    • 13
    This RCN2 antibody is un-conjugated
    Application
    • 12
    • 8
    • 4
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Purification
    Immunogen affinity purified
    Purity
    ≥95 % as determined by SDS-PAGE
    Immunogen
    reticulocalbin 2, EF-hand calcium binding domain
    Isotype
    IgG
    Top Product
    Discover our top product RCN2 Primary Antibody
  • Application Notes
    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide and 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
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    Expiry Date
    12 months
  • Target
    RCN2 (Reticulocalbin 2, EF-Hand Calcium Binding Domain (RCN2))
    Alternative Name
    RCN2 (RCN2 Products)
    Synonyms
    rcn2 antibody, MGC80678 antibody, si:dkey-24l11.6 antibody, zgc:110594 antibody, LOC733807 antibody, AA408742 antibody, Tcbp49 antibody, E6BP antibody, ERC-55 antibody, ERC55 antibody, TCBP49 antibody, reticulocalbin 2 S homeolog antibody, reticulocalbin 2 antibody, rcn2.S antibody, RCN2 antibody, rcn2 antibody, Rcn2 antibody
    Background
    Synonyms:ERC55 Background:The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    37 kDa
    Gene ID
    5955
    UniProt
    Q14257
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