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DENND4C antibody (AbBy Fluor® 750)

This anti-DENND4C antibody is a Rabbit Polyclonal antibody detecting DENND4C in WB and IF (p). Suitable for Human, Mouse and Rat.
Catalog No. ABIN5001173

Quick Overview for DENND4C antibody (AbBy Fluor® 750) (ABIN5001173)

Target

DENND4C (DENN/MADD Domain Containing 4C (DENND4C))

Reactivity

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Human, Mouse, Rat

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This DENND4C antibody is conjugated to AbBy Fluor® 750

Application

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

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human DENND4C

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 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

    DENND4C (DENN/MADD Domain Containing 4C (DENND4C))

    Alternative Name

    DENND4C

    Background

    Synonyms: C9orf55, C9orf55B, DEN4C_HUMAN, DENN domain-containing protein 4C, DENN/MADD domain containing 4C, DENND4C.

    Background: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4 % of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.

    Gene ID

    55667
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