Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5)
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
Produktmerkmale
This is a synthetic peptide designed for use in combination with anti-SLC17A5 antibody (Catalog #: ARP43932_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
Each Investigator should determine their own optimal working dilution for specific applications.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Konzentration
1 mg/mL
Buffer
Final peptide concentration is 1 mg/mL in PBS.
Handhabung
Avoid repeated freeze-thaw cycles.
Lagerung
-20 °C
Informationen zur Lagerung
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
Target
Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5)
Synonyme
AST Peptide, ISSD Peptide, NSD Peptide, SD Peptide, SIALIN Peptide, SIASD Peptide, SLD Peptide, sialin Peptide, got2 Peptide, zgc:66329 Peptide, 4631416G20Rik Peptide, 4732491M05 Peptide, SP55 Peptide, sb:cb809 Peptide, zgc:153077 Peptide, solute carrier family 17 member 5 Peptide, solute carrier family 17 member 5 S homeolog Peptide, glutamic-oxaloacetic transaminase 2a, mitochondrial Peptide, solute carrier family 17 (anion/sugar transporter), member 5 Peptide, solute carrier family 17 (acidic sugar transporter), member 5 Peptide, SLC17A5 Peptide, slc17a5.S Peptide, got2a Peptide, Slc17a5 Peptide, slc17a5 Peptide
Hintergrund
SLC17A5 is a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in SLC17A5 gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form.This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.