SLC29A3 anticorps (C-Term) (Cy3)

N° du produit ABIN8040060

L’anticorps anti-SLC29A3 Polyclonal Lapin est utilisé pour la détection de SLC29A3 dans des échantillons de Humain. Il a été validé pour FACS.

Aperçu rapide pour SLC29A3 anticorps (C-Term) (Cy3) (ABIN8040060)

Antigène: SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC29A3 est conjugé à/à la Cy3

Application: Flow Cytometry (FACS)

Détail du produit anti-SLC29A3 anticorps (Cy3)

Épitope: C-Term

Fonction: Anti-SLC29A3 Antibody Cy3 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Purification: Immunogen affinity purified.

Immunogène: A synthetic peptide corresponding to a sequence at the C-terminus of human SLC29A3.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur SLC29A3

Antigène: SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Autre désignation: SLC29A3

Sujet:

Background: This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.

Gene Full Name: solute carrier family 29 member 3

ID gène: 55315

UniProt: Q9BZD2