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CCDC112 antibody

The Rabbit Polyclonal anti-CCDC112 antibody (ABIN7246133) specifically detects CCDC112 in ELISA and IHC. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7246133
-15% Promotion 2026
$457.98
$538.80
save $80.82 (-15 %)
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Quick Overview for CCDC112 antibody (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

  • 11
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CCDC112 antibody is un-conjugated

Application

  • 18
  • 15
  • 13
  • 13
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human CCDC112

    Isotype

    IgG
  • 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

    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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