PEX16 Antikörper (AA 100-180)

Produktnummer ABIN7230596

Der Kaninchen Polyklonal anti-PEX16 Antikörper (ABIN7230596) detektiert spezifisch PEX16 in WB und ELISA. Dieser Antikörper reagiert spezifisch mit Proben aus Human und Maus.

Kurzübersicht für PEX16 Antikörper (AA 100-180) (ABIN7230596)

Target: PEX16 (Peroxisomal Biogenesis Factor 16 (PEX16))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX16 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-PEX16 Antikörper

Bindungsspezifität: AA 100-180

Verwendungszweck: Rabbit Anti-PEX16 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of PEX16 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 PEX16 protein at AA range: 100-180

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 PEX16

Target: PEX16 (Peroxisomal Biogenesis Factor 16 (PEX16))

Andere Bezeichnung: PEX16

Hintergrund: Peroxisomal membrane protein PEX16, Peroxin-16, Peroxisomal biogenesis factor 16PEX16 (Peroxisomal Biogenesis Factor 16) is a Protein Coding gene. Diseases associated with PEX16 include Peroxisome Biogenesis Disorder 8B and Peroxisome Biogenesis Disorder 8A. Among its related pathways are Peroxisome. The protein encoded by PEX16 is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of PEX16 product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for PEX16 and two variants have been described.

Molekulargewicht: 36kD

Gen-ID: 9409

UniProt: Q9Y5Y5