SLC19A2 anticorps (C-Term)
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- Antigène Voir toutes SLC19A2 Anticorps
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
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Épitope
- C-Term
- Reactivité
- Humain, Cheval, Lapin, Cobaye, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SLC19A2 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- LGLEITTQFL IYASYFALIA VVFLASGAVS VMKKCRKLED PQSSSQVTTS
- Homologie
- Guinea Pig: 79%, Horse: 86%, Human: 100%, Rabbit: 79%, Rat: 86%
- Attributs du produit
- This is a rabbit polyclonal antibody against SLC19A2. It was validated on Western Blot.
- Purification
- Affinity Purified
- Top Product
- Discover our top product SLC19A2 Anticorps primaire
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- Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
- Commentaires
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Antigen size: 497 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Antigène
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- Autre désignation
- SLC19A2 (SLC19A2 Produits)
- Synonymes
- anticorps SLC19A2, anticorps TC1, anticorps THMD1, anticorps THT1, anticorps THTR1, anticorps TRMA, anticorps solute carrier family 19 member 2, anticorps solute carrier family 19 (thiamine transporter), member 2, anticorps Slc19a2, anticorps SLC19A2, anticorps slc19a2
- 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 Interaction Partner: UBC, CERS2, ELAVL1,
Protein Size: 497 - Poids moléculaire
- 55 kDa
- ID gène
- 10560
- NCBI Accession
- NM_006996, NP_008927
- UniProt
- O60779
- Pathways
- Dicarboxylic Acid Transport
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