REEP5 Antikörper (AbBy Fluor® 350)

Produktnummer ABIN1402965

Dieses Anti-REEP5-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von REEP5 in WB und IF (p). Geeignet für Human, Maus und Ratte.

Kurzübersicht für REEP5 Antikörper (AbBy Fluor® 350) (ABIN1402965)

Target: REEP5 (Receptor Accessory Protein 5 (REEP5))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser REEP5 Antikörper ist konjugiert mit AbBy Fluor® 350

Applikation: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-REEP5 Antikörper (AbBy Fluor® 350)

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human REEP5

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu REEP5

Target: REEP5 (Receptor Accessory Protein 5 (REEP5))

Andere Bezeichnung: REEP5

Hintergrund:

Synonyms: C5orf18, DP1, Polyposis locus protein 1, Receptor expression enhancing protein 5, Receptor expression-enhancing protein 5, TB2, TB2 protein, D5S346,REEP5_HUMAN.

Background: REEP5 is a 189 amino acid multi-pass membrane protein. Thought to promote the functional cell surface expression of olfactory receptors, REEP5 belongs to the DP1 family and is encoded by a gene that maps to chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Gen-ID: 7905

Pathways: SARS-CoV-2 Protein Interaktom