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CCDC115 antibody (AA 1-180)

The Rabbit Polyclonal anti-CCDC115 antibody is suitable to detect CCDC115 in samples from Human. It has been validated for WB, ELISA, IF, IHC (p) and FACS.
Catalog No. ABIN7868265
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for CCDC115 antibody (AA 1-180) (ABIN7868265)

Target

See all CCDC115 Antibodies
CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

Reactivity

  • 10
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 6
  • 4
Rabbit

Clonality

  • 8
  • 2
Polyclonal

Conjugate

  • 10
This CCDC115 antibody is un-conjugated

Application

  • 10
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-180

    Purpose

    CCDC115 Antibody

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids M1-A180) was used as the immunogen for the CCDC115 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the CCDC115 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the CCDC115 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

    Alternative Name

    CCDC115

    Background

    Coiled-coil domain containing 115 is a protein that in humans is encoded by the CCDC115 gene. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans.

    UniProt

    Q96NT0
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