Anti-SLC25A19 antibody

Polyclonal

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Q9HC21

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.

SLC25A19

Rabbit polyclonal against SLC25A19

Mitochondrion Inner Membrane
Multi-Pass Membrane Protein

WB 1:500-1:2000

Mitochondrial Thiamine Pyrophosphate Carrier
Mitochondrial Uncoupling Protein 1
Solute Carrier Family 25 Member 19

TPC_HUMAN