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ALMS1 anticorps (AA 3400-3450)

ALMS1 Reactivité: Humain IP Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7452260
  • Antigène Voir toutes ALMS1 Anticorps
    ALMS1 (Alstrom Syndrome 1 (ALMS1))
    Épitope
    • 4
    • 3
    • 2
    • 1
    • 1
    AA 3400-3450
    Reactivité
    • 11
    • 1
    Humain
    Hôte
    • 10
    • 1
    Lapin
    Clonalité
    • 10
    Polyclonal
    Conjugué
    • 8
    • 1
    • 1
    • 1
    Cet anticorp ALMS1 est non-conjugé
    Application
    • 7
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Fonction
    Rabbit anti-ALMS1 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogène
    between AA 3400 and 3450
    Isotype
    IgG
    Top Product
    Discover our top product ALMS1 Anticorps primaire
  • Indications d'application

    IP: 2 - 5 μg/mg lysate

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

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    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
    4 °C
    Date de péremption
    12 months
  • Antigène
    ALMS1 (Alstrom Syndrome 1 (ALMS1))
    Autre désignation
    ALMS1 (ALMS1 Produits)
    Synonymes
    anticorps ALMS1, anticorps ALSS, anticorps bbb, anticorps ALMS1, centrosome and basal body associated protein, anticorps Alstrom syndrome 1, anticorps putative ALMS1-like protein, anticorps ALMS1, centrosome and basal body associated, anticorps ALMS1, anticorps alms1, anticorps LOC459325, anticorps Alms1
    Sujet
    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.
    ID gène
    7840
    UniProt
    Q8TCU4
    Pathways
    Sensory Perception of Sound, Carbohydrate Homeostasis, M Phase
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