Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

BRWD1-AS2 anticorps (Cy7)

L’anticorps Lapin Polyclonal anti-BRWD1-AS2 a été validé pour WB et IF (p). Il convient pour détecter BRWD1-AS2 dans des échantillons de Humain.
N° du produit ABIN1423634

Aperçu rapide pour BRWD1-AS2 anticorps (Cy7) (ABIN1423634)

Antigène

BRWD1-AS2

Reactivité

Humain

Hôte

  • 16
Lapin

Clonalité

  • 16
Polyclonal

Conjugué

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp BRWD1-AS2 est conjugé à/à la Cy7

Application

  • 16
  • 12
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  •  Réactivité croisée

    Humain

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human C21orf87

    Isotype

    IgG
  • Indications d'application

    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Date de péremption

    12 months
  • Antigène

    BRWD1-AS2

    Autre désignation

    C21orf87

    Sujet

    Synonyms: chromosome 21 open reading frame 87, BRIT2_HUMAN.

    Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterization.

    ID gène

    257357
Vous êtes ici:
Chat with us!