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RDH5 anticorps

RDH5 Reactivité: Humain, Souris, Rat IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6571537
  • Antigène Voir toutes RDH5 Anticorps
    RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 6
    • 1
    • 1
    Lapin
    Clonalité
    • 8
    Polyclonal
    Conjugué
    • 8
    Cet anticorp RDH5 est non-conjugé
    Application
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human RDH5 (NP_002896.2).
    Isotype
    IgG
    Top Product
    Discover our top product RDH5 Anticorps primaire
  • Indications d'application
    IF 1:50-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
    Autre désignation
    RDH5 (RDH5 Produits)
    Synonymes
    anticorps 9cRDH, anticorps HSD17B9, anticorps RDH1, anticorps SDR9C5, anticorps RDHB, anticorps MGC84134, anticorps RDH5, anticorps rdh1, anticorps hsd17b9, anticorps im:6901729, anticorps si:dkey-102c8.5, anticorps 9-cis, anticorps AI987873, anticorps RDH4, anticorps cRDH, anticorps retinol dehydrogenase 5, anticorps retinol dehydrogenase 1, anticorps retinol dehydrogenase 5 L homeolog, anticorps retinol dehydrogenase 5 (11-cis/9-cis), anticorps RDH5, anticorps rdh1, anticorps rdh5.L, anticorps rdh5, anticorps Rdh5
    Sujet
    This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.
    Poids moléculaire

    Observed_MW: 38kDa

    Calculated_MW: 34kDa

    ID gène
    5959
    UniProt
    Q92781
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