PDZD9 anticorps (AA 50-100) (Cy7)

N° du produit ABIN1421636

Détail du produit anti-PDZD9 anticorps (Cy7)

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

Épitope: AA 50-100

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PDZD9 est conjugé à/à la Cy7

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human PDZD9

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

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

Date de péremption: 12 months

Détails sur PDZD9

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

Autre désignation: PDZD9 (PDZD9 Produits)

Synonymes: anticorps C16orf65, anticorps C25H16orf65, anticorps 4930408O21Rik, anticorps LRRGT00105, anticorps PDZ domain containing 9, anticorps PDZD9, anticorps Pdzd9

Sujet:

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.

ID gène: 255762

UniProt: Q8IXQ8