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CCDC117 antibody (AA 148-250) (FITC)

The Rabbit Polyclonal anti-CCDC117 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect CCDC117 in samples from Human.
Catalog No. ABIN887051

Quick Overview for CCDC117 antibody (AA 148-250) (FITC) (ABIN887051)

Target

See all CCDC117 Antibodies
CCDC117 (Coiled-Coil Domain Containing 117 (CCDC117))

Reactivity

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  • 1
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This CCDC117 antibody is conjugated to FITC

Application

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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

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    AA 148-250

    Predicted Reactivity

    Human,Mouse,Rat,Dog,Cow,Sheep,Horse

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human CCDC117

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    CCDC117 (Coiled-Coil Domain Containing 117 (CCDC117))

    Alternative Name

    CCDC117

    Background

    Synonyms: CC117_HUMAN, Ccdc117, Coiled-coil domain-containing protein 117.

    Background: CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein Bcr-Abl, a potent cell proliferation activator found in several types of leukemias.

    Gene ID

    150275
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