Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2) (C-Term) Peptide
SLC19A2
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits SLC19A2
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- Protein Region
- C-Term
- Origine
- Humain
- Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Séquence
- LGLEITTQFL IYASYFALIA VVFLASGAVS VMKKCRKLED PQSSSQVTTS
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-SLC19A2 Antibody. 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.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- Synonymes
- SLC19A2 Peptide, TC1 Peptide, THMD1 Peptide, THT1 Peptide, THTR1 Peptide, TRMA Peptide, solute carrier family 19 member 2 Peptide, solute carrier family 19 (thiamine transporter), member 2 Peptide, Slc19a2 Peptide, SLC19A2 Peptide, slc19a2 Peptide
- Sujet
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This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.
Alias Symbols: TC1, THT1, THTR1, TRMA, THMD1
Protein Size: 497 - Poids moléculaire
- 55 kDa
- ID gène
- 10560
- NCBI Accession
- NM_006996, NP_008927
- UniProt
- O60779
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