SLC25A19 Polyclonal Antibody

SLC25A19 Polyclonal Antibody

Catalog Number:
A001509004RED
Mfr. No.:
RD265956A
Price:
$347
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      • Overview
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          Background

          This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene.

      • Properties
        • Host
          rabbit
          Isotype
          IgG
          Reactivity
          human; mouse
          Immunogen
          Recombinant fusion protein of human SLC25A19 (NP_068380.3).
          Purification
          Affinity purification
          Conjugate
          Unconjugated
          Formulation
          PBS with 0.02% sodium azide, 50% glycerol, pH7.3
          Storage
          Store at -20°C. Avoid freeze-thaw cycles.
          Concentration
          1 mg/mL
          Antigen
          SLC25A19, DNC, MCPHA, MUP1, THMD3, THMD4, TPC (Gene ID:60386; UniProt:Q9HC21)

          * For reference only.

      • Applications
        • Application
          IF
        • Application Dilutions
          IF 1:50-1:200

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