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ALMS1 Antikörper (AA 3400-3450)

ALMS1 Reaktivität: Human IP Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7452260
  • Target Alle ALMS1 Antikörper anzeigen
    ALMS1 (Alstrom Syndrome 1 (ALMS1))
    Bindungsspezifität
    • 4
    • 3
    • 2
    • 1
    • 1
    AA 3400-3450
    Reaktivität
    • 11
    • 1
    Human
    Wirt
    • 10
    • 1
    Kaninchen
    Klonalität
    • 10
    Polyklonal
    Konjugat
    • 8
    • 1
    • 1
    • 1
    Dieser ALMS1 Antikörper ist unkonjugiert
    Applikation
    • 7
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Verwendungszweck
    Rabbit anti-ALMS1 Antibody, Affinity Purified
    Aufreinigung
    Affinity Purified
    Immunogen
    between AA 3400 and 3450
    Isotyp
    IgG
    Top Product
    Discover our top product ALMS1 Primärantikörper
  • Applikationshinweise

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-ALMS1 antibody A301-815A.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C
    Haltbarkeit
    12 months
  • Target
    ALMS1 (Alstrom Syndrome 1 (ALMS1))
    Andere Bezeichnung
    ALMS1 (ALMS1 Produkte)
    Synonyme
    ALMS1 antikoerper, ALSS antikoerper, bbb antikoerper, ALMS1, centrosome and basal body associated protein antikoerper, Alstrom syndrome 1 antikoerper, putative ALMS1-like protein antikoerper, ALMS1, centrosome and basal body associated antikoerper, ALMS1 antikoerper, alms1 antikoerper, LOC459325 antikoerper, Alms1 antikoerper
    Hintergrund
    Background: Mutations in the ALMS1 gene are the cause of Alstrom syndrome, a rare autosomal recessive disease characterized by type 2 diabetes mellitus, obesity, cardiomyopathy, and neurosensory defects such as cone-rod retinal dystrophy, and hearing loss. In the cell, ALMS1 localizes to basal bodies of ciliated cells and centrosomes and is thus a member of proteins associated with genetic ciliopathies.
    Gen-ID
    7840
    UniProt
    Q8TCU4
    Pathways
    Sensory Perception of Sound, Carbohydrate Homeostasis, M Phase
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