SLC29A3 anticorps (C-Term)

N° du produit ABIN8040058

Cet anticorps anti-SLC29A3 Polyclonal Lapin (ABIN8040058) détecte spécifiquement SLC29A3 dans IHC. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour SLC29A3 anticorps (C-Term) (ABIN8040058)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC29A3 est non-conjugé

Application: Immunohistochemistry (IHC)

Détail du produit anti-SLC29A3 anticorps

Épitope: C-Term

Fonction: Anti-SLC29A3 Antibody

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

Attributs du produit: Anti-SLC29A3 Antibody-1. Tested in IHC applications. This antibody reacts with Human.

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: Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20 °C for six months. Avoid repeated freezing and thawing.

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