PRRT2 anticorps (AA 180-230)

N° du produit ABIN6991846

Cet anticorps Lapin Polyclonal détecte spécifiquement PRRT2 dans WB, ELISA, IF et IHC (p). Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour PRRT2 anticorps (AA 180-230) (ABIN6991846)

Antigène: PRRT2 (Proline-Rich Transmembrane Protein 2 (PRRT2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PRRT2 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-PRRT2 anticorps

Épitope: AA 180-230

Specificité: Multiple isoforms of PRRT2 are known to exist.

Purification: PRRT2 Antibody is affinity chromatography purified via peptide column.

Immunogène: PRRT2 antibody was raised against a 18 amino acid peptide near the center of human PRRT2 . The immunogen is located within amino acids 180 - 230 of PRRT2.

Isotype: IgG

Information d'application

Indications d'application: PRRT2 Antibody can be used for detection of PRRT2 by Western blot at 1 μ,g/mL.

Antibody validated: Western Blot in mouse samples, Immunohistochemistry in rat samples and Immunofluorescence in rat samples. All other applications and species not yet tested.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PRRT2 Antibody is supplied in PBS containing 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C,4 °C

Stockage commentaire: PRRT2 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.

Détails sur PRRT2

Antigène: PRRT2 (Proline-Rich Transmembrane Protein 2 (PRRT2))

Autre désignation: PRRT2

Sujet: PRRT2 Antibody: The proline-rich transmembrane protein 2 (PRRT2) contains a proline-rich domain in its N-terminal half and is predominantly expressed in brain and spinal cord in embryonic and postnatal stages. While little is known of the function of this protein, mutations in PRRT2 have been shown to be the causative gene of paroxysmal kinesigenic dyskinesia, which is characterized by recurrent, brief attacks of abnormal involuntary movements induced by sudden voluntary movements. Recent studies have shown that PRRT2 may also be involved in some forms of benign familial infantile epilepsy (BFIE), an autosomal dominant epilepsy syndrome.

Poids moléculaire: Predicted: 43 kDa

Observed: 44 kDa

ID gène: 112476

NCBI Accession: NP_001243371

UniProt: Q7Z6L0