Overview

  • Product name
  • Description
    Rabbit polyclonal to PRRT2
  • Host species
    Rabbit
  • Tested applications
    Suitable for: WBmore details
  • Species reactivity
    Reacts with: Mouse, Rat, Human
  • Immunogen

    An 18 amino acid synthetic peptide derived from near the center of Human PRRT2 (NP_001243371).

  • Positive control
    • Mouse brain tissue lysate.

Properties

  • Form
    Liquid
  • Storage instructions
    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term.
  • Storage buffer
    Preservative: 0.02% Sodium azide
    Constituent: 99% PBS
  • Concentration information loading...
  • Purity
    Immunogen affinity purified
  • Clonality
    Polyclonal
  • Isotype
    IgG
  • Research areas

Applications

Our Abpromise guarantee covers the use of ab167130 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 Use a concentration of 1 - 2 µg/ml. Predicted molecular weight: 35, 40 kDa.

Target

  • Involvement in disease
    Episodic kinesigenic dyskinesia 1 (EKD1) [MIM:128200]: An autosomal dominant neurologic condition characterized by recurrent and brief attacks of abnormal involuntary movements, triggered by sudden voluntary movement. These attacks usually have onset during childhood or early adulthood and can involve dystonic postures, chorea, or athetosis. Note=The disease is caused by mutations affecting the gene represented in this entry. Disease-causing mutations that produce truncation of the C-terminus of the protein alter subcellular location, from plasma membrane to cytosplasm (PubMed:22101681).
    Convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA) [MIM:602066]: A syndrome characterized by clinical features of benign familial infantile seizures and episodic kinesigenic dyskinesia. Benign familial infantile seizures is a disorder characterized by afebrile seizures occurring during the first year of life, without neurologic sequelae. Paroxysmal choreoathetosis is a disorder of involuntary movements characterized by attacks that occur spontaneously or are induced by a variety of stimuli. Note=The disease is caused by mutations affecting the gene represented in this entry.
    Seizures, benign familial infantile 2 (BFIS2) [MIM:605751]: An autosomal dominant disorder in which afebrile seizures occur in clusters during the first year of life, without neurologic sequelae. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Sequence similarities
    Belongs to the CD225/Dispanin family.
  • Cellular localization
    Cell membrane. Cell junction > synapse.
  • Information by UniProt
  • Database links
  • Alternative names
    • interferon induced transmembrane protein domain containing 1 antibody
    • BFIC2 antibody
    • BFIS2 antibody
    • Dispanin subfamily B member 3 antibody
    • DSPB3 antibody
    • Dystonia 10 antibody
    • DYT10 antibody
    • EKD1 antibody
    • FICCA antibody
    • FLJ25513 antibody
    • ICCA antibody
    • IFITMD1 antibody
    • Infantile convulsions and paroxysmal choreoathetosis antibody
    • PKC antibody
    • Proline rich transmembrane protein 2 antibody
    • Proline-rich transmembrane protein 2 antibody
    • PRRT2 antibody
    • PRRT2_HUMAN antibody
    see all

Images

  • Anti-PRRT2 antibody (ab167130) at 1 µg/ml + Mouse brain tissue lysate at 15 µg

    Predicted band size: 35, 40 kDa

References

ab167130 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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