Anti-KCTD17 antibody produced in rabbit, 1 X 100 µL (HPA018459-100UL)

The gene KCTD17 (potassium channel tetramerization domain containing 17) is mapped to human chromosome 22q12.3. KCDC17 is abundantly expressed in brain regions, particularly putamen and thalamus. The protein is present in the cytoplasm with fine reticular pattern. The protein contains amino-terminal bric-a-brack, tram-track, broad complex/poxvirus zinc finger (BTB/POZ) domain. All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry. The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information. Solution in phosphate-buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. BTB/POZ domain-containing protein KCTD17 recombinant protein epitope signature tag (PrEST) BTB/POZ domain-containing protein KCTD17 (potassium channel tetramerization domain containing 17) interacts with trichoplein. KCTD17 with Cul3-RING E3 ligases (CRL3s) causes poly-ubiquitination and subsequent degradation of trichoplein. These events are important to initiate axoneme extension during ciliogenesis. Mutations in KCDC17 are associated with myoclonus-dystonia, a rare movement disorder. Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section. Every Prestige Antibody is tested in the following ways: •IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues. •Protein array of 364 human recombinant protein fragments.

Read Less