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BSCL2 Antikörper

BSCL2 Reaktivität: Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6293870
  • Target Alle BSCL2 Antikörper anzeigen
    BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))
    Reaktivität
    • 27
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Maus, Ratte
    Wirt
    • 22
    • 4
    • 1
    Kaninchen
    Klonalität
    • 25
    • 2
    Polyklonal
    Konjugat
    • 17
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser BSCL2 Antikörper ist unkonjugiert
    Applikation
    • 27
    • 17
    • 14
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Aufreinigung
    Affinity purification
    Immunogen
    A synthetic peptide of human BSCL2
    Isotyp
    IgG
    Top Product
    Discover our top product BSCL2 Primärantikörper
  • Applikationshinweise
    WB 1:500 - 1:2000
    Kommentare

    Expressed in motor neurons in the spinal cord and cortical neurons in the frontal lobe (at protein level), Highly expressed in brain, testis and adipose tissue

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20C. Avoid freeze / thaw cycles.
  • Target
    BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))
    Andere Bezeichnung
    BSCL2 (BSCL2 Produkte)
    Synonyme
    GNG3LG antikoerper, HMN5 antikoerper, SPG17 antikoerper, 2900097C17Rik antikoerper, AI046355 antikoerper, Gng3lg antikoerper, BSCL2, seipin lipid droplet biogenesis associated antikoerper, Berardinelli-Seip congenital lipodystrophy 2 (seipin) antikoerper, BSCL2 antikoerper, Bscl2 antikoerper
    Hintergrund
    This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2).
    Molekulargewicht
    44.392 kDa
    Gen-ID
    26580
    UniProt
    Q96G97
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