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BSCL2 anticorps

BSCL2 Reactivité: Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6293870
  • Antigène Voir toutes BSCL2 Anticorps
    BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))
    Reactivité
    • 26
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Souris, Rat
    Hôte
    • 21
    • 4
    • 1
    Lapin
    Clonalité
    • 24
    • 2
    Polyclonal
    Conjugué
    • 16
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp BSCL2 est non-conjugé
    Application
    • 26
    • 17
    • 14
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    A synthetic peptide of human BSCL2
    Isotype
    IgG
    Top Product
    Discover our top product BSCL2 Anticorps primaire
  • Indications d'application
    WB 1:500 - 1:2000
    Commentaires

    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

    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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
    -20 °C
    Stockage commentaire
    Store at -20C. Avoid freeze / thaw cycles.
  • Antigène
    BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))
    Autre désignation
    BSCL2 (BSCL2 Produits)
    Synonymes
    anticorps GNG3LG, anticorps HMN5, anticorps SPG17, anticorps 2900097C17Rik, anticorps AI046355, anticorps Gng3lg, anticorps BSCL2, seipin lipid droplet biogenesis associated, anticorps Berardinelli-Seip congenital lipodystrophy 2 (seipin), anticorps BSCL2, anticorps Bscl2
    Sujet
    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).
    Poids moléculaire
    44.392 kDa
    ID gène
    26580
    UniProt
    Q96G97
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