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CCDC50 antibody

This anti-CCDC50 antibody is a Rabbit Polyclonal antibody detecting CCDC50 in WB, IHC (p), ICC and IF. Suitable for Human.
Catalog No. ABIN7465103

Quick Overview for CCDC50 antibody (ABIN7465103)

Target

See all CCDC50 Antibodies
CCDC50 (Coiled-Coil Domain Containing 50 (CCDC50))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This CCDC50 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Ymer. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:1000-1:10000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: 293T , A431 , HeLa

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    CCDC50 (Coiled-Coil Domain Containing 50 (CCDC50))

    Alternative Name

    coiled-coil domain containing 50

    Background

    Coiled-coil domain containing 50 , C3orf6 , DFNA44 , YMER,This gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq]

    Molecular Weight

    36 kDa

    Gene ID

    152137

    UniProt

    Q8IVM0
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