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CUBN antibody

CUBN Reactivity: Human, Rat, Mouse WB, IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7073601
  • Target See all CUBN Antibodies
    CUBN (Cubilin (Intrinsic Factor-Cobalamin Receptor) (CUBN))
    Reactivity
    Human, Rat, Mouse
    Host
    • 43
    • 1
    Rabbit
    Clonality
    • 35
    • 9
    Polyclonal
    Conjugate
    • 12
    • 10
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CUBN antibody is un-conjugated
    Application
    • 21
    • 15
    • 13
    • 13
    • 8
    • 7
    • 4
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    Cross-Reactivity
    Human, Rat
    Purification
    Affinity purification
    Immunogen
    Recombinant protein corresponding to Mouse Cubilin
  • Application Notes
    WB (M,R) 1:500-1:1000, IHC/IF (H,M,R) 1:650-1:1300
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % 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
    -20 °C
  • Target
    CUBN (Cubilin (Intrinsic Factor-Cobalamin Receptor) (CUBN))
    Alternative Name
    Cubilin (CUBN Products)
    Synonyms
    GP280 antibody, IFCR antibody, MGA1 antibody, AA408369 antibody, AL022750 antibody, D2Wsu88e antibody, gp280 antibody, cubilin antibody, cubilin (intrinsic factor-cobalamin receptor) antibody, LOC411053 antibody, CUBN antibody, cubn antibody, Cubn antibody
    Background
    Cubilin is an endocytic receptor that lacks a classical transmembrane region. It is a multidomain receptor that contains an amino terminal 110 residue segment followed by 8 epidermal growth factor (EGF)-like repeats and a contiguous stretch of 27 CUB domains. Cubilin acts as a receptor for intrinsic factor-vitamin B12 complexes. Cubilin is located within the epithelium of intestine and kidney. Mutations in Cubilin may play a role in autosomal recessive megaloblastic anemia also known as Imerslund-Grasbeck's disease, which causes intestinal malabsorption of vitamin B12.
    Molecular Weight
    399 kDa
    Gene ID
    65969
    NCBI Accession
    NP_001074553
    UniProt
    Q9JLB4
    Pathways
    Metabolism of Steroid Hormones and Vitamin D, Lipid Metabolism
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