PDZD9 Antikörper (AA 50-100) (Alexa Fluor 488)

Produktnummer ABIN1403764

Produktdetails anti-PDZD9 Antikörper (Alexa Fluor 488)

Target: PDZD9 (PDZ Domain Containing 9 (PDZD9))

Bindungsspezifität: AA 50-100

Reaktivität: Human, Ratte, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PDZD9 Antikörper ist konjugiert mit Alexa Fluor 488

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human PDZD9

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 PDZD9

Target: PDZD9 (PDZ Domain Containing 9 (PDZD9))

Andere Bezeichnung: PDZD9 (PDZD9 Produkte)

Synonyme: C16orf65 antikoerper, C25H16orf65 antikoerper, 4930408O21Rik antikoerper, LRRGT00105 antikoerper, PDZ domain containing 9 antikoerper, PDZD9 antikoerper, Pdzd9 antikoerper

Hintergrund:

Synonyms: PDZ domain containing 9, PDZ domain containing protein 9, PDZD 9, PDZK-9.\, PDZD9_HUMAN.

Background: PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.

Gen-ID: 255762

UniProt: Q8IXQ8