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PRDM8 anticorps (AA 14-405)

L’anticorps anti-PRDM8 Polyclonal Lapin est utilisé pour la détection de PRDM8 dans des échantillons de Humain. Il a été validé pour WB, ELISA, IF et FACS.
N° du produit ABIN7870635
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour PRDM8 anticorps (AA 14-405) (ABIN7870635)

Antigène

Voir toutes PRDM8 Anticorps
PRDM8 (PR Domain Containing 8 (PRDM8))

Reactivité

  • 20
  • 5
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Humain

Hôte

  • 20
Lapin

Clonalité

  • 20
Polyclonal

Conjugué

  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PRDM8 est non-conjugé

Application

  • 19
  • 10
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Épitope

    • 9
    • 8
    • 2
    • 1
    • 1
    • 1
    AA 14-405

    Fonction

    PRDM8 Antibody / PR domain zinc finger protein 8

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids D14-D405) was used as the immunogen for the PRDM8 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the PRDM8 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the PRDM8 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    PRDM8 (PR Domain Containing 8 (PRDM8))

    Autre désignation

    PRDM8

    Sujet

    This gene encodes a protein that belongs to a conserved family of histone methyltransferases that predominantly act as negative regulators of transcription. The encoded protein contains an N-terminal Su(var)3-9, Enhancer-of-zeste, and Trithorax (SET) domain and a double zinc-finger domain. Knockout of this gene in mouse results in mistargeting by neurons of the dorsal telencephalon, abnormal itch-like behavior, and impaired differentiation of rod bipolar cells. In humans, the protein has been shown to interact with the phosphatase laforin and the ubiquitin ligase malin, which regulate glycogen construction in the cytoplasm. Alternative splicing results in multiple transcript variants.

    UniProt

    Q9NQV8
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