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FAM13B Antikörper

FAM13B Reaktivität: Human, Maus ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7243301
  • Target Alle FAM13B Produkte
    FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
    Reaktivität
    Human, Maus
    Wirt
    • 36
    • 1
    Kaninchen
    Klonalität
    • 37
    Polyklonal
    Konjugat
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser FAM13B Antikörper ist unkonjugiert
    Applikation
    • 30
    • 15
    • 13
    • 13
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Synthetic peptide of human FAM13B
    Isotyp
    IgG
  • Applikationshinweise
    IHC 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FAM13B (Family with Sequence Similarity 13, Member B (FAM13B))
    Andere Bezeichnung
    FAM13B (FAM13B Produkte)
    Synonyme
    ARHGAP49 antikoerper, C5orf5 antikoerper, FAM13B1 antikoerper, KHCHP antikoerper, N61 antikoerper, 2610024E20Rik antikoerper, AW060714 antikoerper, AW546153 antikoerper, family with sequence similarity 13 member B antikoerper, family with sequence similarity 13, member B antikoerper, FAM13B antikoerper, Fam13b antikoerper
    Hintergrund
    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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