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SLC33A1 Antikörper

SLC33A1 Reaktivität: Human, Maus, Ratte WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2432289
  • Target Alle SLC33A1 Antikörper anzeigen
    SLC33A1 (Solute Carrier Family 33 Member 1 (SLC33A1))
    Reaktivität
    • 26
    • 23
    • 10
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 34
    • 4
    Kaninchen
    Klonalität
    • 36
    • 2
    Polyklonal
    Konjugat
    • 13
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser SLC33A1 Antikörper ist unkonjugiert
    Applikation
    • 27
    • 13
    • 13
    • 12
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB), ELISA
    Aufreinigung
    Affinity purification
    Immunogen
    Synthetic peptide of human SLC33A1
    Isotyp
    IgG
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    Discover our top product SLC33A1 Primärantikörper
  • Applikationshinweise
    WB 1:1000-1:5000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Konservierungsmittel
    Sodium azide
    Handhabung
    Avoid freeze / thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SLC33A1 (Solute Carrier Family 33 Member 1 (SLC33A1))
    Andere Bezeichnung
    SLC33A1 (SLC33A1 Produkte)
    Synonyme
    zgc:63693 antikoerper, ACATN antikoerper, AT-1 antikoerper, AT1 antikoerper, CCHLND antikoerper, SPG42 antikoerper, AI315656 antikoerper, AI788741 antikoerper, Acatn antikoerper, D630022N01Rik antikoerper, solute carrier family 33 (acetyl-CoA transporter), member 1 antikoerper, solute carrier family 33 member 1 antikoerper, slc33a1 antikoerper, SLC33A1 antikoerper, Slc33a1 antikoerper
    Hintergrund
    The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene.
    Molekulargewicht
    Calculated MW: 61 kDa
    NCBI Accession
    NP_004724
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