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DYNAP antibody (N-Term)

The Rabbit Polyclonal anti-DYNAP antibody has been validated for WB and EIA. It is suitable to detect DYNAP in samples from Human.
Catalog No. ABIN950798

Quick Overview for DYNAP antibody (N-Term) (ABIN950798)

Target

DYNAP (Dynactin Associated Protein (DYNAP))

Reactivity

Human

Host

  • 17
Rabbit

Clonality

  • 17
Polyclonal

Conjugate

  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DYNAP antibody is un-conjugated

Application

  • 9
  • 8
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 8
    • 2
    • 1
    AA 5-34, N-Term

    Specificity

    This antibody reacts to C18orf26.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human C18orf26

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) sodium azide as preservative

    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 freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    DYNAP (Dynactin Associated Protein (DYNAP))

    Alternative Name

    C18orf26

    Background

    C18orf26 (chromosome 18 open reading frame 26) is a 210 amino acid single pass membrane protein that is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.Synonyms: Uncharacterized protein

    Gene ID

    284254

    NCBI Accession

    NP_775900
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