Recombinant Galectin 9 anticorps (Biotin)

N° du produit ABIN7851617

Cet anticorps anti-Galectin 9 Chimeric Human conjugué à Biotin (Clone DMC279) (ABIN7851617) détecte spécifiquement Galectin 9 dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Recombinant Galectin 9 anticorps (Biotin) (ABIN7851617)

Antigène: Galectin 9 (LGALS9) (Lectin, Galactoside-Binding, Soluble, 9 (LGALS9))

Type d'anticorp: Recombinant Antibody

Fragment: Fc fragment

Reactivité: Humain

Hôte: Human, Lapin

Clonalité: Chimeric

Conjugué: Cet anticorp Galectin 9 est conjugé à/à la Biotin

Application: Flow Cytometry (FACS)

Clone: DMC279

Détail du produit anti-Galectin 9 anticorps (Biotin)

Fonction: Biotinylated Anti-Galectin 9 antibody(DMC279), IgG1 Chimeric mAb

Purification: Purified from cell culture supernatant by affinity chromatography

Isotype: IgG1

Information d'application

Indications d'application: Flow Cyt 1:100

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Please see Certificate of Analysis for specific instructions of reconstitution.

Buffer: Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

Stock: -20 °C,-80 °C

Stockage commentaire: Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

Date de péremption: 12 months

Détails sur Galectin 9

Antigène: Galectin 9 (LGALS9) (Lectin, Galactoside-Binding, Soluble, 9 (LGALS9))

Autre désignation: Galectin 9

Sujet: The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. The protein encoded by this gene is an S-type lectin. It is overexpressed in Hodgkin's disease tissue and might participate in the interaction between the HandRS cells with their surrounding cells and might thus play a role in the pathogenesis of this disease and:or its associated immunodeficiency. Multiple alternatively spliced transcript variants have been found for this gene.

UniProt: O00182