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BRWD1-AS2 Antikörper (Alexa Fluor 594)

Reaktivität: Human IF (p) Wirt: Kaninchen Polyclonal Alexa Fluor 594
Produktnummer ABIN2810771
$470.46
Zzgl. Versandkosten $45.00
100 μL
Lieferung in 11 bis 16 Werktagen
  • Target See all BRWD1-AS2 products
    BRWD1-AS2
    Reaktivität
    Human
    Wirt
    • 16
    Kaninchen
    Klonalität
    • 16
    Polyklonal
    Konjugat
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser BRWD1-AS2 Antikörper ist konjugiert mit Alexa Fluor 594
    Applikation
    • 12
    • 5
    • 3
    • 1
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C21orf87
    Isotyp
    IgG
  • Applikationshinweise
    IF(IHC-P) 1:50-200
    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.
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C/-80 °C
    Informationen zur Lagerung
    Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles
    Haltbarkeit
    12 months
  • Target
    BRWD1-AS2
    Andere Bezeichnung
    C21orf87 (BRWD1-AS2 Produkte)
    Synonyme
    BRWD1-IT2 antikoerper, C21orf87 antikoerper, NCRNA00257 antikoerper, BRWD1 antisense RNA 2 antikoerper, BRWD1-AS2 antikoerper
    Hintergrund

    The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterization.

    Synonyms: chromosome 21 open reading frame 87, BRIT2_HUMAN.

    Gen-ID
    257357
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