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Over 1000 citations of OriGene cDNA clones
1,2,4-Triazolyl octahydropyrrolo[2,3-b]pyrroles: A new series of potent and selective dopamine D3 receptor antagonists Bioorg. Med. Chem. Apr 2016 [DRD3]

A role for ABCG2 beyond drug transport: regulation of autophagy Autophagy Mar 2016 [ABCG2]

An extended U2AF(65)-RNA-binding domain recognizes the 3' splice site signal NATURE COMMUNICATIONS Mar 2016 [U2AF2]

Aptamer-miRNA-212 Conjugate Sensitizes NSCLC Cells to TRAIL Molecular Therapy nucleic acid Mar 2016 [AXL]

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SLC29A1 (NM_001078177 ) Stable Cell Line

Catalog #:SL500074Price:$12888    technical questions?
Description:Human Equilibrative Nucleoside Transporter ENT1 Stable Cell Line - HeLa
Gene:SLC29A1
Other names: ENT1
Host CellHeLa
cDNA Clone:
Format:Cryopreserved cells, 3 x 10E6 cells/vial
Mycoplasma:Negative by MycoAlert Kit, Lonza
Cell Line Validation:Western blot
Background:Equilibrative Nucleoside Transporter (ENT1), is a member of the equilibrative nucleoside transporter family. The gene encodes a transmembrane glycoprotein that localizes to the plasma and mitochondrial membranes and mediates the cellular uptake of nucleosides from the surrounding medium. The protein is categorized as an equilibrative (as opposed to concentrative) transporter that is sensitive to inhibition by nitrobenzylthioinosine (NBMPR). Nucleoside transporters are required for nucleotide synthesis in cells that lack de novo nucleoside synthesis pathways, and are also necessary for the uptake of cytotoxic nucleosides that are used for cancer and viral chemotherapies.
Figure 1. Immunoprecipation analysis in HeLa/ENT1 by using mAb-agrose against DDK (FLAG) tag (Cat# TA50011-100). 15 ug of membrane protein was used for this immunoprecipation. Membrane protein concentrations were measured by BCA kit (Thermo Scientific Inc.). Lane A: Membrane protein from HeLa/ENT1-pCMV Entry stable cell line. The specific band between 64KD and 97 KD is ENT1. The 25KD band is the mAb light chain and the 50KD band is the heavy chain. Lane B: Membrane protein from NIH3T3 cells tranfected with pCMV-Entry vectors was used as negative control. Lane C: Membrane protein from NIH3T3 cells was used as negative control.

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