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ACTL10 Antikörper (AA 21-100) (Biotin)

ACTL10 Reaktivität: Ratte IHC (p), ELISA, IHC (fro) Wirt: Kaninchen Polyclonal Biotin
Produktnummer ABIN1700217
  • Target Alle ACTL10 Produkte
    ACTL10 (Actin-Like 10 (ACTL10))
    Bindungsspezifität
    AA 21-100
    Reaktivität
    Ratte
    Wirt
    • 14
    Kaninchen
    Klonalität
    • 14
    Polyklonal
    Konjugat
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser ACTL10 Antikörper ist konjugiert mit Biotin
    Applikation
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
    Kreuzreaktivität
    Ratte
    Homologie
    Human,Mouse
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C20orf134
    Isotyp
    IgG
  • Applikationshinweise
    IHC-P 1:200-400
    IHC-F 1:100-500
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C for 12 months.
    Haltbarkeit
    12 months
  • Target
    ACTL10 (Actin-Like 10 (ACTL10))
    Andere Bezeichnung
    C20orf134 (ACTL10 Produkte)
    Synonyme
    C20orf134 antikoerper, dJ63M2.2 antikoerper, 1700007I08Rik antikoerper, actin like 10 antikoerper, actin-like 10 antikoerper, ACTL10 antikoerper, Actl10 antikoerper
    Hintergrund

    Synonyms: C20orf134, CT134_HUMAN, Putative uncharacterized actin family protein C20orf134.

    Background: C20orf134 is a 245 amino acid secreted protein that belongs to the Actin family and is encoded by a gene which maps to human chromosome 20. Comprising approximately 2 % of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception.

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