SLC19A2 anticorps (C-Term)

N° du produit ABIN971707

Détail du produit anti-SLC19A2 anticorps

Antigène: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Épitope: C-Term

Reactivité: Humain, Cheval, Lapin, Cobaye, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC19A2 est non-conjugé

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

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 497 AA

Restrictions: For Research Use only

Stockage

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.

Détails sur SLC19A2

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: 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