• Product name
    Anti-SLC12A1 antibody [EPR11842]
    See all SLC12A1 primary antibodies
  • Description
    Rabbit monoclonal [EPR11842] to SLC12A1
  • Host species
  • Specificity
    The homology between SLC12A1 and SLC12A2 is 67%, so ab171747 may cross react with SLC12A2. We haven't performed any laboratory testing about this.
  • Tested applications
    Suitable for: WB, Flow Cytmore details
    Unsuitable for: ICC/IF,IHC-P or IP
  • Species reactivity
    Reacts with: Mouse, Rat, Human
  • Immunogen

    Recombinant fragment within Human SLC12A1. The exact sequence is proprietary.
    Database link: Q13621

  • Positive control
    • 293T, Human fetal kidney, K562 and WI-38 cell lysates; permeabilized K562 cells.
  • General notes



    Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMab® patents

    This product is a recombinant rabbit monoclonal antibody.


  • Form
  • Storage instructions
    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
  • Storage buffer
    pH: 7.20
    Preservative: 0.01% Sodium azide
    Constituents: 9% PBS, 40% Glycerol, 0.05% BSA, 50% Tissue culture supernatant
  • Purity
    Tissue culture supernatant
  • Clonality
  • Clone number
  • Isotype
  • Research areas


Our Abpromise guarantee covers the use of ab171747 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB 1/1000 - 1/10000. Predicted molecular weight: 121 kDa.
Flow Cyt 1/100 - 1/500.

ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody.


  • Application notes
    Is unsuitable for ICC/IF,IHC-P or IP.
  • Target

    • Function
      Electrically silent transporter system. Mediates sodium and chloride reabsorption. Plays a vital role in the regulation of ionic balance and cell volume.
    • Tissue specificity
      Kidney specific.
    • Involvement in disease
      Defects in SLC12A1 are the cause of Bartter syndrome type 1 (BS1) [MIM:601678]. BS refers to a group of autosomal recessive disorders characterized by impaired salt reabsorption in the thick ascending loop of Henle with pronounced salt wasting, hypokalemic metabolic alkalosis, and varying degrees of hypercalciuria. BS1 is a life-threatening condition beginning in utero, with marked fetal polyuria that leads to polyhydramnios and premature delivery. Another hallmark of BS1 is a marked hypercalciuria and, as a secondary consequence, the development of nephrocalcinosis and osteopenia.
    • Sequence similarities
      Belongs to the SLC12A transporter family.
    • Cellular localization
    • Information by UniProt
    • Database links
    • Alternative names
      • BSC1 antibody
      • Bumetanide sensitive sodium 3 antibody
      • Bumetanide-sensitive sodium-(potassium)-chloride cotransporter 2 antibody
      • Kidney specific Na K Cl symporter antibody
      • Kidney-specific Na-K-Cl symporter antibody
      • MGC48843 antibody
      • Na K 2Cl cotransporter antibody
      • NKCC2 antibody
      • potassiumchloride cotransporter 2 antibody
      • S12A1_HUMAN antibody
      • Slc12a1 antibody
      • sodium potassium chloride cotransporter 2 antibody
      • solute carrier family 12 (sodium/potassium/chloride transporters) antibody
      • Solute carrier family 12 member 1 antibody
      see all


    • All lanes : Anti-SLC12A1 antibody [EPR11842] (ab171747) at 1/1000 dilution

      Lane 1 : 293T cell lysates
      Lane 2 : Human fetal kidney lysates
      Lane 3 : K562 cell lysates
      Lane 4 : WI-38 cell lysates

      Lysates/proteins at 10 µg per lane.

      Predicted band size: 121 kDa

    • Flow cytometric analysis of permeabilized K562 cells labeling SLC12A1 with ab171747 at 1/100 dilution (red), compared with a rabbit IgG (negative) (green).


    This product has been referenced in:
    • Sasaki S  et al. A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle. BMC Genomics 17:724 (2016). Cow . Read more (PubMed: 27613513) »
    • Teng F  et al. Treatment with an SLC12A1 antagonist inhibits tumorigenesis in a subset of hepatocellular carcinomas. Oncotarget 7:53571-53582 (2016). IHC . Read more (PubMed: 27447551) »
    See all 3 Publications for this product

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