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SLC33A1 antibody

SLC33A1 Reactivity: Human, Mouse, Rat WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2426903
  • Target See all SLC33A1 Antibodies
    SLC33A1 (Solute Carrier Family 33 Member 1 (SLC33A1))
    Reactivity
    • 26
    • 23
    • 10
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 34
    • 4
    Rabbit
    Clonality
    • 36
    • 2
    Polyclonal
    Conjugate
    • 13
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This SLC33A1 antibody is un-conjugated
    Application
    • 27
    • 13
    • 13
    • 12
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB), ELISA
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human SLC33A1
    Isotype
    IgG
    Top Product
    Discover our top product SLC33A1 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SLC33A1 (Solute Carrier Family 33 Member 1 (SLC33A1))
    Alternative Name
    SLC33A1 (SLC33A1 Products)
    Synonyms
    zgc:63693 antibody, ACATN antibody, AT-1 antibody, AT1 antibody, CCHLND antibody, SPG42 antibody, AI315656 antibody, AI788741 antibody, Acatn antibody, D630022N01Rik antibody, solute carrier family 33 (acetyl-CoA transporter), member 1 antibody, solute carrier family 33 member 1 antibody, slc33a1 antibody, SLC33A1 antibody, Slc33a1 antibody
    Background
    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.
    Molecular Weight
    Calculated MW: 61 kDa
    NCBI Accession
    NP_004724
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