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CCDC134 antibody (AA 11-120) (Biotin)

This Rabbit Polyclonal antibody specifically detects CCDC134 in ELISA, IHC (p) and IHC (fro). It exhibits reactivity toward Mouse.
Catalog No. ABIN887167

Quick Overview for CCDC134 antibody (AA 11-120) (Biotin) (ABIN887167)

Target

See all CCDC134 Antibodies
CCDC134 (Coiled-Coil Domain Containing 134 (CCDC134))

Reactivity

  • 21
  • 17
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse

Host

  • 35
Rabbit

Clonality

  • 35
Polyclonal

Conjugate

  • 11
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CCDC134 antibody is conjugated to Biotin

Application

  • 17
  • 13
  • 13
  • 13
  • 10
  • 6
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Binding Specificity

    • 14
    • 8
    • 8
    • 4
    • 3
    • 2
    • 1
    • 1
    AA 11-120

    Cross-Reactivity

    Mouse

    Predicted Reactivity

    Human,Rat,Dog,Cow,Horse

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human CCDC134

    Isotype

    IgG
  • Application Notes

    IHC-P 1:200-400
    IHC-F 1:100-500

    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 for 12 months.

    Expiry Date

    12 months
  • Target

    CCDC134 (Coiled-Coil Domain Containing 134 (CCDC134))

    Alternative Name

    CCDC134

    Background

    Synonyms: CC134_HUMAN, ccdc134, coiled-coil domain containing 134, Coiled-coil domain-containing protein 134, dJ821D11.3, FLJ22349, MGC21013.

    Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.

    Gene ID

    79879
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