ARG43456

anti-SLC29A3 / ENT3 antibody

anti-SLC29A3 / ENT3 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes SLC29A3 / ENT3
Tested Reactivity Ms, Rat
Predict Reactivity Hu
Tested Application IHC-P, WB
Specificity This SLC29A3 / ENT antibody is predicted to not cross-react with other SLC29 proteins.
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name SLC29A3 / ENT3
Antigen Species Human
Immunogen A 19 amino acid peptide within aa. N-terminal of Human SLC29A3 / ENT3.
Conjugation Un-conjugated
Protein Full Name Equilibrative nucleoside transporter 3
Alternate Names Equilibrative nucleoside transporter 3; ENT3; HJCD; PHID; HCLAP; Solute carrier family 29 member 3; UNQ717/PRO1380; hENT3

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P5 μg/mL for immunohistochemistry and 20 μg/mL for immunofluorescence
WB1 - 2 μg/mL
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 50-70 kDa (70 kda might be protein with PTM)

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS and 0.02% Sodium azide.
Preservative 0.02% Sodium azide
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 353307 Rat SLC29A3

GeneID: 71279 Mouse SLC29A3

Swiss-port # Q80WK7 Rat Equilibrative nucleoside transporter 3

Swiss-port # Q99P65 Mouse Equilibrative nucleoside transporter 3

Gene Symbol SLC29A3
Gene Full Name solute carrier family 29 member 3
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.[provided by RefSeq, Mar 2010]
Function Mediates both influx and efflux of nucleosides across the membrane (equilibrative transporter). Mediates transport of adenine, adenosine and uridine, as well as several nucleoside analog drugs, such as anticancer and antiviral agents, including cladribine, cordycepin, tubercidin and AZT. Does not transport hypoxanthine.[provided by uniprot]
Cellular Localization Endosome, Lysosome, Membrane
Calculated MW 51.8 kDa
PTM Glycoprotein, Phosphoprotein