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CC2D2A antibody (N-Term)

This anti-CC2D2A antibody is a Rabbit Polyclonal antibody detecting CC2D2A in WB. Suitable for Human, Mouse and Guinea Pig.
Catalog No. ABIN2790202

Quick Overview for CC2D2A antibody (N-Term) (ABIN2790202)

Target

See all CC2D2A Antibodies
CC2D2A (Coiled-Coil and C2 Domain Containing 2A (CC2D2A))

Reactivity

Human, Mouse, Guinea Pig

Host

  • 2
Rabbit

Clonality

  • 2
Polyclonal

Conjugate

  • 2
This CC2D2A antibody is un-conjugated

Application

  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    N-Term

    Sequence

    EDADMGRQNK NSKVRRQPRK KQKPTPFSRA CWQILPHLSA GVPLLGWEHP

    Predicted Reactivity

    Guinea Pig: 77%, Human: 100%, Mouse: 92%

    Characteristics

    This is a rabbit polyclonal antibody against CC2D2A. It was validated on Western Blot.

    Purification

    Affinity Purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N-terminal region of Human CC2D2A
  • Application Notes

    Optimal working dilutions should be determined experimentally by the investigator.

    Comment

    Antigen size: 122 AA

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    Lot specific

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    CC2D2A (Coiled-Coil and C2 Domain Containing 2A (CC2D2A))

    Alternative Name

    CC2D2A

    Background

    This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants.
    Alias Symbols: JBTS9, KIAA1345, MKS6
    Protein Interaction Partner: UBC,
    Protein Size: 122

    Molecular Weight

    14 kDa

    Gene ID

    57545

    NCBI Accession

    NM_020785, NP_065836

    UniProt

    E7EP21
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