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CCDC50 antibody (AA 1-50)

This Rabbit Polyclonal antibody specifically detects CCDC50 in IP. It exhibits reactivity toward Human.
Catalog No. ABIN7452478

Quick Overview for CCDC50 antibody (AA 1-50) (ABIN7452478)

Target

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

Reactivity

  • 38
  • 19
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 37
  • 1
Rabbit

Clonality

  • 38
Polyclonal

Conjugate

  • 19
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CCDC50 antibody is un-conjugated

Application

  • 36
  • 13
  • 13
  • 13
  • 11
  • 6
  • 3
  • 3
  • 2
  • 2
Immunoprecipitation (IP)
  • Binding Specificity

    • 15
    • 7
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-50

    Purpose

    Rabbit anti-Ymer Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 1 and 50

    Isotype

    IgG
  • Application Notes

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-Ymer antibody ABIN7452172.

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    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

    4 °C

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    Ymer

    Background

    Background: Ymer was identified in a mass spectrometric study of epidermal growth factor signaling. It is a cytoplasmic tyrosine-phosphorylated protein that bears multiple ubiquitin-interacting domains. Recently Ymer has been implicated as a negative regulator of the NF-kappaB signaling pathway. Mutations in the gene that encodes Ymer, CCDC50, are the cause of autosomal dominant non-syndromic sensorineural deafness type 44.

    Gene ID

    152137

    NCBI Accession

    NP_777568

    UniProt

    Q8IVM0
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