SLC29A3 Proteins

(Solute Carrier Family 29 Member 3 (SLC29A3))

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].

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SLC29A3 Protein (AA 1-475) (His tag)

custom-made SLC29A3 Origin: Human Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)

AlphaFold protein structure predicition of Human Recombinant SLC29A3 Protein, UniprotID Q9BZD2

3 images

Catalog No. ABIN7545924

Details

SLC29A3 Protein (AA 1-475) (His tag)

custom-made SLC29A3 Origin: Mouse Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)

AlphaFold protein structure predicition of Mouse Recombinant Slc29a3 Protein, UniprotID Q99P65

3 images

Catalog No. ABIN7560452

Details

SLC29A3 Protein (AA 1-475) (Strep Tag)

custom-made SLC29A3 Origin: Human Host: Cell-free protein synthesis (CFPS) Recombinant approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC). WB, ELISA, SDS

Catalog No. ABIN3117903

Details

SLC29A3 Protein (AA 1-475) (Strep Tag)

custom-made SLC29A3 Origin: Mouse Host: Cell-free protein synthesis (CFPS) Recombinant approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC). WB, ELISA, SDS

Catalog No. ABIN3128133