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DYNAP anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-DYNAP a été validé pour WB. Il convient pour détecter DYNAP dans des échantillons de Humain.
N° du produit ABIN1539422

Aperçu rapide pour DYNAP anticorps (N-Term) (ABIN1539422)

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
  • 1
Western Blotting (WB)

Clone

RB35932
  • Épitope

    • 7
    • 2
    • 2
    AA 6-34, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This C18orf26 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 6-34 amino acids from the N-terminal region of human C18orf26.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    C18orf26 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • 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.

    ID gène

    284254

    NCBI Accession

    NP_775900

    UniProt

    Q8N1N2
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