PEX1 Antikörper (AA 256-1266) (Fluoro594)

Produktnummer ABIN8020719

Der Kaninchen Polyklonal anti-PEX1 Antikörper wird verwendet zum Nachweis von PEX1 in Proben von Human. Er wurde validiert für FACS.

Kurzübersicht für PEX1 Antikörper (AA 256-1266) (Fluoro594) (ABIN8020719)

Target: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX1 Antikörper ist konjugiert mit Fluoro594

Applikation: Flow Cytometry (FACS)

Produktdetails anti-PEX1 Antikörper (Fluoro594)

Bindungsspezifität: AA 256-1266

Verwendungszweck: Anti-PEX1 Antibody Fluoro594 Conjugated

Kreuzreaktivität (Details): No cross-reactivity with other proteins

Homologie: Human PEX1 shares 83.4% amino acid (aa) sequence identity with mouse PEX1.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human PEX1 recombinant protein (Position: Q256-R1266). Human PEX1 shares 83.4% amino acid (aa) sequence identity with mouse PEX1.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, Optimal dilutions should be determined by end users.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Haltbarkeit: 12 months

Details zu PEX1

Target: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Andere Bezeichnung: PEX1

Hintergrund:

Background: This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene.

Gene Full Name: peroxisomal biogenesis factor 1

Gen-ID: 5189

UniProt: O43933