Anti-SLC17A5 Monoclonal Antibody (A-10H7)

Anti-SLC17A5 Monoclonal Antibody (A-10H7)

Cat No: ASZ1C1685

Summary
Host Species:
Mouse
Species Reactivity:
Human
Applications:
Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
Clone ID:
A-10H7
Clonality:
Monoclonal

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Product Information
Subcat Description Isotype Antibody Modification Conjugate Size Price Quantity
ASZ1C1685 Anti-SLC17A5 Antibody (A-10H7) Mouse IgG None $460
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  • Anti-SLC17A5 Monoclonal Antibody (A-10H7)
    • Product Description:
      The Anti-SLC17A5 antibody is a mouse monoclonal antibody recommended for immunohistochemistry, immunocytochemistry, western blot, immunoprecipitation and other applications. This antibody specifically targets human SLC17A5.
      Applications:
      Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
      Source:
      Mouse
      Target:
      SLC17A5
      Target Species:
      Human
      Specificity:
      This antibody reacts with human Solute Carrier Family 17 Member 5 (SLC17A5).
      Clonality:
      Monoclonal
      Clone ID:
      A-10H7
      Purification:
      The antibody was purified by affinity chromatography.
      Purity:
      >95% as determined by SDS-PAGE
      Concentration:
      1 mg/mL
      Form:
      Liquid
      Formulation:
      Contact us for custom product formulation.
      Preservative:
      0.05% Proclin 300
      Shipping:
      Shipped at 4°C.
      Storage:
      This antibody can be stored at 2°C-8°C for one month. For longer storage, store at -20°C. Avoid repeated freeze-thaw cycles.
  • Anti-SLC17A5 Monoclonal Antibody (A-10H7) Applications
    • Recommended Dilution:
      Western Blot: 1:500-1:5000
      Immunohistochemistry: 1:50-1:200
      Immunocytochemistry: 1:50-1:200
      Note:
      Optimal dilutions/concentrations should be determined by the end user.
Protein Name
Sialin
Introduction
This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form.
Alternative Names
AST; ISSD; NSD; SD; SIALIN; SIASD; SLD
Gene ID
UniProt
Related Disease
Salla disease (SD)
Subcellular Location
Basolateral cell membrane
Cell Line Specificity
Low cancer specificity
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