SLC25A15 Antibody

• Background:

  This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.

• NCBI Gene ID:

  10166

• Swiss Prot:

  Q9Y619

• Host:

  Rabbit

• Reactivity:

  Human

• Immunogen:

  Recombinant fusion protein containing a sequence corresponding to amino acids 1-301 of human SLC25A15 (NP_055067.1) .

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Primary Antibodies

• Field of Research:

  Other

• Purification:

  Affinity purification

• Positive Control:

  HeLa

• Concentration:

  Batch dependent

• Buffer:

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

• Modification:

  None

• Shipping Conditions:

  Blue Ice

• Storage Conditions:

  Store at -20˚ C. Avoid freeze / thaw cycles.

• Calculated Molecular Weight:

  Observed: 35kDa

• Fragment:

  IgG

• Applications Notes:

  WB: 1:200 - 1:2000

• Symbol:

  SLC25A15

• Positive Control 2:

  MCF7

• NCBI Official Name:

  Solute carrier family 25 member 15

• NCBI Organism:

  Homo sapiens

• Other Product Names:

  D13S327, HHH, ORC1, ORNT1, mitochondrial ornithine transporter 1, ornithine transporter 1, solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15

• Tested Applications:

  WB

• Physical Properties:

  Liquid