SLC29A3 anticorps (N-Term)

N° du produit ABIN656792

Détail du produit anti-SLC29A3 anticorps

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

Épitope: AA 21-50, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC29A3 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This SLC29A3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 21-50 amino acids from the N-terminal region of human SLC29A3.

Clone: RB32652

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: SLC29A3 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Date de péremption: 6 months

Détails sur SLC29A3

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

Autre désignation: SLC29A3 (SLC29A3 Produits)

Synonymes: anticorps ENT3, anticorps HCLAP, anticorps HJCD, anticorps PHID, anticorps Ent3, anticorps 4933435C21Rik, anticorps AW987637, anticorps solute carrier family 29 member 3, anticorps solute carrier family 29 (nucleoside transporters), member 3, anticorps SLC29A3, anticorps Slc29a3

Sujet: 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.

Poids moléculaire: 51815

ID gène: 55315

NCBI Accession: NP_001167569, NP_060814

UniProt: Q9BZD2