SLC29A3 Antibody (N-term) Blocking peptide
€363.00
In stock
SKU
AC-BP12865a
Background:
This gene encodes a nucleoside transporter. The encodedprotein plays a role in cellular uptake of nucleosides,nucleobases, and their related analogs. Mutations in this gene havebeen associated with H syndrome, which is characterized bycutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly,heart anomalies, and hypogonadism. A related disorder, PHID(pigmented hypertrichosis with insulin-dependent diabetesmellitus), has also been associated with mutations at this locus.Alternatively spliced transcript variants have been described.
Other Names:
Equilibrative nucleoside transporter 3, hENT3, Solute carrier family 29 member 3, SLC29A3, ENT3
Gene Name: SLC29A3 (HGNC:23096)
Gene ID: 55315
Primary Accession: Q9BZD2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a nucleoside transporter. The encodedprotein plays a role in cellular uptake of nucleosides,nucleobases, and their related analogs. Mutations in this gene havebeen associated with H syndrome, which is characterized bycutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly,heart anomalies, and hypogonadism. A related disorder, PHID(pigmented hypertrichosis with insulin-dependent diabetesmellitus), has also been associated with mutations at this locus.Alternatively spliced transcript variants have been described.
Other Names:
Equilibrative nucleoside transporter 3, hENT3, Solute carrier family 29 member 3, SLC29A3, ENT3
Gene Name: SLC29A3 (HGNC:23096)
Gene ID: 55315
Primary Accession: Q9BZD2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
| Is Featured? | No |
|---|
Write Your Own Review