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CCDC112 antibody

CCDC112 Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7246133
  • Target See all CCDC112 Antibodies
    CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))
    Reactivity
    • 42
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 41
    • 1
    Rabbit
    Clonality
    • 42
    Polyclonal
    Conjugate
    • 12
    • 5
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CCDC112 antibody is un-conjugated
    Application
    • 23
    • 21
    • 13
    • 13
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human CCDC112
    Isotype
    IgG
    Top Product
    Discover our top product CCDC112 Primary Antibody
  • Application Notes
    IHC 1:40-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))
    Alternative Name
    CCDC112 (CCDC112 Products)
    Synonyms
    CCDC112 antibody, RGD1561942 antibody, MBC1 antibody, 8430438M01Rik antibody, AW108467 antibody, coiled-coil domain containing 112 antibody, CCDC112 antibody, Ccdc112 antibody, ccdc112 antibody
    Background
    CCDC112 (coiled-coil domain containing 112), also known as MBC1 (mutated in bladder cancer 1), is a 446 amino acid protein. The gene encoding CCDC112 is located on chromosome 5. Due to alternative splicing events, CCDC112 exists as two isoforms. Chromosome 5 comprises about 6 % of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
    UniProt
    Q8NEF3
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