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FASTKD5 anticorps

FASTKD5 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2423441
  • Antigène Voir toutes FASTKD5 Anticorps
    FASTKD5 (FAST Kinase Domains 5 (FASTKD5))
    Reactivité
    • 35
    • 10
    • 1
    Humain
    Hôte
    • 34
    • 1
    Lapin
    Clonalité
    • 35
    Polyclonal
    Conjugué
    • 10
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FASTKD5 est non-conjugé
    Application
    • 13
    • 13
    • 11
    • 7
    • 4
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human FASTKD5
    Isotype
    IgG
    Top Product
    Discover our top product FASTKD5 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.6 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    FASTKD5 (FAST Kinase Domains 5 (FASTKD5))
    Autre désignation
    FASTKD5 (FASTKD5 Produits)
    Synonymes
    anticorps dJ1187M17.5, anticorps C78212, anticorps mKIAA1792, anticorps Fastkd5-ps1, anticorps RGD1563839, anticorps FAST kinase domains 5, anticorps U-box domain containing 5, anticorps FASTKD5, anticorps UBOX5, anticorps Fastkd5
    Sujet
    Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis which are thought important for seminal production and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.
    NCBI Accession
    NP_068598
    Pathways
    SARS-CoV-2 Protein Interactome
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