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FAM13B anticorps

FAM13B Reactivité: Humain, Souris ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7243301
  • Antigène Tous les produits FAM13B
    FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
    Reactivité
    Humain, Souris
    Hôte
    • 36
    • 1
    Lapin
    Clonalité
    • 37
    Polyclonal
    Conjugué
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FAM13B est non-conjugé
    Application
    • 30
    • 15
    • 13
    • 13
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human FAM13B
    Isotype
    IgG
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
    Autre désignation
    FAM13B (FAM13B Produits)
    Synonymes
    anticorps ARHGAP49, anticorps C5orf5, anticorps FAM13B1, anticorps KHCHP, anticorps N61, anticorps 2610024E20Rik, anticorps AW060714, anticorps AW546153, anticorps family with sequence similarity 13 member B, anticorps family with sequence similarity 13, member B, anticorps FAM13B, anticorps Fam13b
    Sujet
    FAM13B is a 915 amino acid protein that is encoded by a gene that maps to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
    NCBI Accession
    NP_057687
    UniProt
    Q9NYF5
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