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Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (AA 479-492), (Intracellular) antibody

SLC17A5 Reactivity: Mouse WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7043679
  • Target See all Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) Antibodies
    Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5)
    Binding Specificity
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 479-492, Intracellular
    Reactivity
    • 12
    • 7
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Mouse
    Host
    • 13
    • 1
    • 1
    Rabbit
    Clonality
    • 14
    • 1
    Polyclonal
    Conjugate
    • 13
    • 1
    • 1
    Un-conjugated
    Application
    • 15
    • 7
    • 6
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purpose
    A Rabbit Polyclonal Antibody to SLC17A5 (Sialin) Transporter
    Specificity
    Intracellular, C-terminus
    Cross-Reactivity
    Human, Mouse, Rat
    Predicted Reactivity
    14 amino acid residues identical,Rat - 13, human - 12
    Characteristics
    Anti-SLC17A5 (Sialin) Antibody (ABIN7043679, ABIN7045310 and ABIN7045311)) is a highly specific antibody directed against an epitope of the mouse Sialin transporter. The antibody can be used in western blot and immunohistochemistry applications. It has been designed to recognize Sialin from rat, mouse, and human samples.
    Purification
    Affinity purified on immobilized antigen.
    Immunogen

    Immunogen: Synthetic peptide

    Immunogen Sequence: (C)KGEVQSWALSDHHG, corresponding to amino acid residues 479-492 of mouse SLC17A5

    Isotype
    IgG
    Top Product
    Discover our top product SLC17A5 Primary Antibody
  • Application Notes

    Antigen preadsorption control: 1 μg peptide per 1 μg antibody

    Application Dilutions Immunohistochemistry paraffin embedded sections ihc: 1:200

    Application Dilutions Western blot wb: 1:200

    Comment

    Negative Control: BLP-ST015

    Blocking Peptide: BLP-ST015

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    0.2 mL double distilled water (DDW).
    Concentration
    1 mg/mL
    Buffer
    PBS pH 7.4
    Storage
    4 °C,-20 °C
    Storage Comment

    Storage before reconstitution: The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.

    Storage after reconstitution: The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).

  • Target
    Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5)
    Alternative Name
    SLC17A5 (SLC17A5 Products)
    Background
    Sialic acid transporter, H+/sialic acid cotransporter, Vesicular H+/aspartate-glutamate cotransporter,Sialin, encoded by the SLC17A5 gene, is a member of the SLC17 solute carrier family, a group of structurally related polytopic membrane proteins, part of the major facilitator superfamily of transporters. Sialin is a sialic acid transporter located in the lysosomal membrane. In the lysosome, sialic acid residues are sequentially removed from the carbohydrate chain by sialidases and then transported out of the lysosome by the transporter protein sialin1,2. Sialin structure consists of 12 transmembrane helices (TMs). TM4 contains three residues (Arg-168, Glu-175, and His-183) that are highly conserved in the SLC17 family, suggesting that they may participate directly in substrate binding and translocation. In addition, TM4 contains a GXXXG helix packing motif that is important for the expression of sialin. SLC17 family includes several more GXXXG-like motifs located within TMs including GXXXG/S in TM2, G/AXXXG in TM5, and G/S/AXXXGXXXG/T in TM13.Proteins included in the SLC17 family are implicated with inherited neurological and metabolic diseases. Mutations in the SLC17A5 gene cause sialic acid storage diseases including infantile sialic acid storage disease and Salla disease. These conditions are autosomal recessive neurodegenerative disorders characterized by excessive accumulation of sialic acid in the lysosome1,2.

    Alternative names: SLC17A5 (Sialin), Sialic acid transporter, H+/sialic acid cotransporter, Vesicular H+/aspartate-glutamate cotransporter
    Gene ID
    235504
    NCBI Accession
    NM_001382629
    UniProt
    Q8BN82
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