• Product name

    Anti-Syntaxin 16 antibody [EPR9156]
    See all Syntaxin 16 primary antibodies
  • Description

    Rabbit monoclonal [EPR9156] to Syntaxin 16
  • Host species

  • Tested applications

    Suitable for: ICC/IF, WB, IHC-Pmore details
    Unsuitable for: Flow Cyt or IP
  • Species reactivity

    Reacts with: Mouse, Rat, Human
  • Immunogen

    Synthetic peptide within Human Syntaxin 16 aa 50-150. The exact sequence is proprietary.

  • Positive control

    • Human testis and lung adenocarcinoma tissues; HepG2 cells; 293T, HeLa, HepG2 and SH-SY5Y cell lysates.
  • 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 -20ºC.
  • Storage buffer

    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 ab134945 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
ICC/IF 1/100 - 1/250.
WB 1/1000 - 1/10000. Predicted molecular weight: 37 kDa.
IHC-P 1/50 - 1/100. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
  • Application notes
    Is unsuitable for Flow Cyt or IP.
  • Target

    • Function

      SNARE involved in vesicular transport from the late endosomes to the trans-Golgi network.
    • Tissue specificity

    • Involvement in disease

      Genetic variations in STX16 may be a cause of pseudohypoparathyroidism type 1B (PHP1B) [MIM:603233]. Pseudohypoparathyroidism refers to a heterogeneous group of disorders characterized by resistance to parathyroid hormone (PTH). PHP1B is characterized by PTH-resistant hypocalcemia and hyperphosphatemia. Patients affected with PHP1B lack developmental defects characteristic of Albright hereditary osteodystrophy, and typically show no other endocrine abnormalities besides resistance to PTH. In some cases microdeletions involving STX16 appear to cause loss of methylation at exon A/B of the GNAS gene, resulting in PHP1B.
    • Sequence similarities

      Belongs to the syntaxin family.
      Contains 1 t-SNARE coiled-coil homology domain.
    • Cellular localization

      Cytoplasm and Golgi apparatus membrane.
    • Information by UniProt
    • Database links

    • Alternative names

      • hsyn16 antibody
      • MGC90328 antibody
      • Stx16 antibody
      • STX16_HUMAN antibody
      • Syn16 antibody
      • Syntaxin-16 antibody
      see all


    • All lanes : Anti-Syntaxin 16 antibody [EPR9156] (ab134945) at 1/1000 dilution

      Lane 1 : HeLa cell lysate
      Lane 2 : HepG2 cell lysate
      Lane 3 : 293T cell lysate
      Lane 4 : SH-SY5Y cell lysate

      Lysates/proteins at 10 µg per lane.

      All lanes : Standard HRP labelled goat anti-rabbit at 1/2000 dilution

      Developed using the ECL technique.

      Predicted band size: 37 kDa

    • Immunofluorescence staining of HepG2 cells, labelling Syntaxin 16 using ab134945 at a 1/100 dilution (red). Cell nuclei are shown in blue.
    • Immunohistochemical analysis of paraffin-embedded, formalin-fixed Human lung adenocarcinoma tissue, labelling Syntaxin 16 using ab134945 at a 1/50 dilution.
    • Immunohistochemical analysis of paraffin-embedded, formalin-fixed Human testis tissue, labelling Syntaxin 16 using ab134945 at a 1/50 dilution.


    This product has been referenced in:

    • Carpier JM  et al. Rab6-dependent retrograde traffic of LAT controls immune synapse formation and T cell activation. J Exp Med 215:1245-1265 (2018). Read more (PubMed: 29440364) »
    See 1 Publication for this product

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