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DYNAP anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-DYNAP a été validé pour WB et EIA. Il convient pour détecter DYNAP dans des échantillons de Humain.
N° du produit ABIN950798

Aperçu rapide pour DYNAP anticorps (N-Term) (ABIN950798)

Antigène

DYNAP (Dynactin Associated Protein (DYNAP))

Reactivité

Humain

Hôte

  • 17
Lapin

Clonalité

  • 17
Polyclonal

Conjugué

  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DYNAP est non-conjugé

Application

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

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

    Specificité

    This antibody reacts to C18orf26.

    Réactivité croisée (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography on Protein A

    Immunogène

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

    Isotype

    Ig Fraction
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    DYNAP (Dynactin Associated Protein (DYNAP))

    Autre désignation

    C18orf26

    Sujet

    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

    ID gène

    284254

    NCBI Accession

    NP_775900
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