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Rabbit anti-Human SLC19A3 Polyclonal Antibody
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Rabbit anti-Human SLC19A3 Polyclonal Antibody
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This gene encodes a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity. Mutations in this gene cause biotin-responsive basal ganglia disease (BBGD); a recessive disorder manifested in childhood that progresses to chronic encephalopathy,
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SLC19A3 is a member of the reduced folate family of micronutrient transporter genes.Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.http://www.creative-diagnostics.com/Anti-SLC19A3-MAb-172307-144.htm
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SLC19A3 is a member of the reduced folate family of micronutrient transporter genes. It is a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity yet mediates high affinity thiamine uptake propably via a
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