Anti-SLC6A8 Monoclonal Antibody (D-11F10)

Anti-SLC6A8 Monoclonal Antibody (D-11F10)

Cat No: ASZ1C1716

Summary
Host Species:
Mouse
Species Reactivity:
Human
Applications:
Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
Clone ID:
D-11F10
Clonality:
Monoclonal

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Product Information
Subcat Description Isotype Antibody Modification Conjugate Size Price Quantity
ASZ1C1716 Anti-SLC6A8 Antibody (D-11F10) Mouse IgG None $460
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  • Anti-SLC6A8 Monoclonal Antibody (D-11F10)
    • Product Description:
      The Anti-SLC6A8 antibody is a mouse monoclonal antibody recommended for immunohistochemistry, immunocytochemistry, western blot, immunoprecipitation and other applications. This antibody specifically targets human SLC6A8.
      Applications:
      Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
      Source:
      Mouse
      Target:
      SLC6A8
      Target Species:
      Human
      Specificity:
      This antibody reacts with human Solute Carrier Family 6 Member 8 (SLC6A8).
      Clonality:
      Monoclonal
      Clone ID:
      D-11F10
      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:
      0.02% sodium azide
      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-SLC6A8 Monoclonal Antibody (D-11F10) 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
Sodium- and chloride-dependent creatine transporter 1
Introduction
The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene.
Alternative Names
CCDS1; CRT; CRTR; CT1; CTR5
Gene ID
UniProt
Related Disease
Cerebral creatine deficiency syndrome 1 (CCDS1)
Subcellular Location
Cell membrane
Tissue Specificity
Predominantly expressed in skeletal muscle and kidney. Also found in brain, heart, colon, testis and prostate.
Cell Line Specificity
Low cancer specificity
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