Tetraspanin 9 anticorps (AA 180-203) (AbBy Fluor® 680)

N° du produit ABIN5012058

Cet anticorps Lapin Polyclonal détecte spécifiquement Tetraspanin 9 dans WB, FACS et IF (p). Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour Tetraspanin 9 anticorps (AA 180-203) (AbBy Fluor® 680) (ABIN5012058)

Antigène: Tetraspanin 9 (TSPAN9)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Tetraspanin 9 est conjugé à/à la AbBy Fluor® 680

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

Détail du produit anti-Tetraspanin 9 anticorps (AbBy Fluor® 680)

Épitope: AA 180-203

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human TSPAN9

Isotype: IgG

Information d'application

Indications d'application: FCM 1:20-100
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 Tetraspanin 9

Antigène: Tetraspanin 9 (TSPAN9)

Autre désignation: TSPAN9

Sujet:

Synonyms: NET5, NET-5, PP1057, Tetraspanin-9, Tspan-9, Tetraspan NET-5, TSPAN9

Background: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

ID gène: 10867

UniProt: O75954