Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

EVC2 antibody

EVC2 Reactivity: Human, Mouse ELISA, IHC, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7243292
  • Target See all EVC2 Antibodies
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    Reactivity
    Human, Mouse
    Host
    • 14
    • 1
    Rabbit
    Clonality
    • 15
    Polyclonal
    Conjugate
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This EVC2 antibody is un-conjugated
    Application
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human EVC2
    Isotype
    IgG
    Top Product
    Discover our top product EVC2 Primary Antibody
  • Application Notes
    WB 1:200-1:1000, IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
    Alternative Name
    EVC2 (EVC2 Products)
    Synonyms
    EVC2 antibody, LBN antibody, 1110017L09Rik antibody, Lbn antibody, limbin antibody, EvC ciliary complex subunit 2 antibody, EVC2 antibody, Evc2 antibody
    Background
    This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    148 kDa
    NCBI Accession
    NP_667338
    UniProt
    Q86UK5
    Pathways
    Hedgehog Signaling
You are here:
Support