PNKD Antikörper (AA 140-220)

Produktnummer ABIN7230718

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch PNKD in ELISA und WB. Es zeigt Reaktivität gegenüber Proben von Human und Maus.

Kurzübersicht für PNKD Antikörper (AA 140-220) (ABIN7230718)

Target: PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PNKD Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB)

Produktdetails anti-PNKD Antikörper

Bindungsspezifität: AA 140-220

Verwendungszweck: Rabbit Anti-PNKD Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of PNKD protein

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human PNKD protein at AA range: 140-220

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu PNKD

Target: PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

Andere Bezeichnung: PNKD

Hintergrund: Probable hydrolase PNKD, Myofibrillogenesis regulator 1, MR-1, Paroxysmal nonkinesiogenic dyskinesia protein, Trans-activated by hepatitis C virus core protein 2PNKD (Paroxysmal Nonkinesigenic Dyskinesia) is a Protein Coding gene. Diseases associated with PNKD include Familial Paroxysmal Nonkinesigenic Dyskinesia and Paroxysmal Nonkinesigenic Dyskinesia 1. PNKD is thought to play a role in the regulation of myofibrillogenesis. Mutations in PNKD have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants.

Molekulargewicht: 42kD

Gen-ID: 25953

UniProt: Q8N490