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anti-Solute Carrier Family 29 Member 3 (SLC29A3) Antibodies

SLC29A3 encodes a nucleoside transporter. Additionally we are shipping Solute Carrier Family 29 Member 3 Proteins (3) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
SLC29A3 55315 Q9BZD2
SLC29A3 353307 Q80WK7
SLC29A3 71279 Q99P65
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Top anti-Solute Carrier Family 29 Member 3 Antibodies at antibodies-online.com

Showing 10 out of 24 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated IHC (p), WB SLC29A3 Antibody (N-term)  western blot analysis in HepG2 cell line lysates (35ug/lane).This demonstrates the SLC29A3 antibody detected the SLC29A3 protein (arrow). SLC29A3 Antibody (N-term) immunohistochemistry analysis in formalin fixed and paraffin embedded human uterus tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of SLC29A3 Antibody (N-term) for immunohistochemistry.  Clinical relevance has not been evaluated. 400 μL Log in to see 10 to 11 Days
$324.50
Details
Human Rabbit Biotin IHC, ELISA, WB   200 μL Log in to see 8 to 10 Days
$969.83
Details
Human Rabbit Un-conjugated IHC, WB 400 μL Log in to see 6 Days
$457.14
Details
Human Rabbit Un-conjugated IF, IHC (p), ELISA   50 μg Log in to see 8 to 10 Days
$451.00
Details
Human Rabbit Un-conjugated ELISA   200 μL Log in to see 8 to 10 Days
$713.17
Details
Human Rabbit Un-conjugated IHC, ELISA, WB   200 μL Log in to see 11 to 16 Days
$532.71
Details
Human Rabbit PE IHC, ELISA, WB   200 μL Log in to see 16 Days
$710.29
Details
Human Rabbit FITC IHC, ELISA, WB   200 μL Log in to see 16 Days
$710.29
Details
Human Rabbit HRP IHC, ELISA, WB   200 μL Log in to see 16 Days
$710.29
Details
Human Rabbit APC IHC, ELISA, WB   200 μL Log in to see 16 Days
$710.29
Details

SLC29A3 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human , ,


, , , , ,
Rat (Rattus)



Mouse (Murine)



More Antibodies against Solute Carrier Family 29 Member 3 Interaction Partners

Human Solute Carrier Family 29 Member 3 (SLC29A3) interaction partners

  1. novel mutation c.401G>A associated with pigmented hypertrichosis with insulin (show INS Antibodies)-dependent diabetes mellitus syndrome

  2. SLC29A3 genetic polymorphisms may have a role in overall survival in advanced non-small-cell lung cancer treated with gemcitabine

  3. Mutation analysis of the SLC29A3 gene revealed a novel nonsense mutation in H syndrome with agenesis of the inferior vena cava (show CA5A Antibodies).

  4. Homozygous mutation in SLC29A3 in 2 children of consanguineous parents exhibit H syndrome: insulin (show INS Antibodies)-dependent diabetes, hyperpigmentation, hepatosplenomegaly, lymphadenopathy, left ventricular hypertrophy, sensorineural hearing loss. [CASE REPORT]

  5. we describe two unrelated children with DSS (show NR0B1 Antibodies) associated with autosomal recessive inheritance of variants in SLC29A3.

  6. Two novel mutations in the SLC29A3 gene were identified: a homozygous splice site mutation IVS1+2T>1 G, and a homozygous missense mutation c.1157G>1 A (p.R386Q) which substituted highly conserved amino acid residue in a transmembrane domain.

  7. The 'rescue' role played by a normally noncoding mRNA splice variant of SLC29A3, uncovering a new mechanism by which frameshift mutations can be hypomorphic.

  8. severe reductions/losses of hENT3 nucleoside transport functions of hENT3 syndrome mutants

  9. The genotype (CC, TC, IT) and allele distribution of the ENT3 single nudcleotide polymorphism in the patients with lung cancer was not significantly different compared with that in controls (P > 0.05).

  10. analysis of two novel mutations affecting the same amino acid residue of hENT3 in H syndrome [case report]

Mouse (Murine) Solute Carrier Family 29 Member 3 (SLC29A3) interaction partners

  1. study found mice lacking ENT3 developed spontaneous and progressive macrophage-dominated histiocytosis; in absence of ENT3, defective apoptotic cell clearance led to lysosomal nucleoside buildup, elevated intralysosomal pH and altered macrophage function

  2. Mutation analysis of candidate genes within the target interval identified biallelic germline mutations in SLC29A3 in the Faisalabad histiocytosis kindred and in two families reported to have familial Rosai-Dorfman disease.

Solute Carrier Family 29 Member 3 (SLC29A3) Antigen Profile

Protein Summary

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 names and symbols associated with SLC29A3

  • solute carrier family 29 (equilibrative nucleoside transporter), member 3 (SLC29A3) antibody
  • solute carrier family 29 (equilibrative nucleoside transporter), member 3 (Slc29a3) antibody
  • solute carrier family 29 (nucleoside transporters), member 3 (Slc29a3) antibody
  • solute carrier family 29 (nucleoside transporters), member 3 (SLC29A3) antibody
  • 4933435C21Rik antibody
  • AW987637 antibody
  • Ent3 antibody
  • HCLAP antibody
  • HJCD antibody
  • PHID antibody

Protein level used designations for SLC29A3

equilibrative nucleoside transporter 3 , solute carrier family 29 (nucleoside transporters), member 3 , solute carrier family 29 member 3 , mENT3

GENE ID SPECIES
55315 Homo sapiens
353307 Rattus norvegicus
71279 Mus musculus
504503 Bos taurus
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