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SLC25A46 anticorps (AA 1-50)

SLC25A46 Reactivité: Humain IP Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7449139
  • Antigène Voir toutes SLC25A46 Anticorps
    SLC25A46 (Solute Carrier Family 25, Member 46 (SLC25A46))
    Épitope
    • 6
    • 3
    • 2
    • 1
    • 1
    AA 1-50
    Reactivité
    • 16
    • 10
    • 8
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 16
    Lapin
    Clonalité
    • 16
    Polyclonal
    Conjugué
    • 12
    • 2
    • 1
    • 1
    Cet anticorp SLC25A46 est non-conjugé
    Application
    • 12
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Fonction
    Rabbit anti-SLC25A46 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogène
    Between AA 1 and 50
    Isotype
    IgG
    Top Product
    Discover our top product SLC25A46 Anticorps primaire
  • Indications d'application
    8 - 15 μL/mg lysate
    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
    SLC25A46 (Solute Carrier Family 25, Member 46 (SLC25A46))
    Autre désignation
    SLC25A46 (SLC25A46 Produits)
    Synonymes
    anticorps SLC25A46, anticorps MGC152354, anticorps zgc:92767, anticorps slc25a46, anticorps 1200007B05Rik, anticorps AI325987, anticorps RGD1305072, anticorps solute carrier family 25 member 46, anticorps solute carrier family 25, member 46, anticorps solute carrier family 25 member 46 L homeolog, anticorps SLC25A46, anticorps slc25a46, anticorps slc25a46.L, anticorps Slc25a46
    Sujet
    Background: Solute carrier family 25 member 46 (SLC25A46) is a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy [taken from NCBI Entrez Gene (Gene ID: 91137)].
    ID gène
    91137
    UniProt
    Q96AG3
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