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Proline-rich transmembrane protein

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Below are the list of possible Proline-rich transmembrane protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Proline-rich transmembrane protein 1

 Proline-rich transmembrane protein 1 ELISA Kit
 Proline-rich transmembrane protein 1 Recombinant
 Proline-rich transmembrane protein 1 Antibody
Also known as Proline-rich transmembrane protein 1 (Dispanin subfamily D member 1) (DSPD1).
PRRT1: Belongs to the CD225/Dispanin family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, multi-pass

Cellular Component: membrane
 Prrt1 ELISA Kit
 Prrt1 Recombinant
 Prrt1 Antibody
 Ng5 ELISA Kit
 Ng5 Recombinant
 Ng5 Antibody
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Proline-rich transmembrane protein 2

 Proline-rich transmembrane protein 2 ELISA Kit
 Proline-rich transmembrane protein 2 Recombinant
 Proline-rich transmembrane protein 2 Antibody
Also known as Proline-rich transmembrane protein 2 (Dispanin subfamily B member 3) (DSPB3).
PRRT2: Defects in PRRT2 are the cause of episodic kinesigenic dyskinesia type 1 (EKD1). 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 e
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arly adulthood and can involve dystonic postures, chorea, or athetosis. Disease-causing mutations that produce truncation of the C-terminus of the protein alter subcellular location, from plasma membrane to cytosplasm (PubMed:22101681). Defects in PRRT2 are the cause of convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA). 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. Defects in PRRT2 are the cause of seizures, benign familial infantile type 2 (BFIS2). An autosomal dominant disorder in which afebrile seizures occur in clusters during the first year of life, without neurologic sequelae. Belongs to the CD225/Dispanin family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Cellular Component: membrane

Biological Process: neuromuscular process controlling posture
 Prrt2 ELISA Kit
 Prrt2 Recombinant
 Prrt2 Antibody
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Proline-rich transmembrane protein 3

 Proline-rich transmembrane protein 3 ELISA Kit
 Proline-rich transmembrane protein 3 Recombinant
 Proline-rich transmembrane protein 3 Antibody
PRRT3: 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 3p25.3
 PRRT3 ELISA Kit
 PRRT3 Recombinant
 PRRT3 Antibody
 UNQ5823/PRO19642 ELISA Kit
 UNQ5823/PRO19642 Recombinant
 UNQ5823/PRO19642 Antibody
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Proline-rich transmembrane protein 4

 Proline-rich transmembrane protein 4 ELISA Kit
 Proline-rich transmembrane protein 4 Recombinant
 Proline-rich transmembrane protein 4 Antibody
PRRT4: 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Membrane protein, multi-pass
 Prrt4 ELISA Kit
 Prrt4 Recombinant
 Prrt4 Antibody
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