Monocarboxylic acid transporter 1 (SLC16A1) (NM_003051) Human Recombinant Protein

• Background:

  The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]

• Synonyms:

  HHF7; MCT; MCT1; MCT1D

• Gene ID:

  6566

• UniProt:

  P53985, A0A024R0H1

• Accession Number mRNA:

  NM_003051

• Chromosomal Location:

  1p13.2

• Expression System:

  HEK293T

• Tag:

  C-Myc/DDK

• Concentration:

  >50 ug/mL as determined by microplate BCA method

• Purity:

  > 80% as determined by SDS-PAGE and Coomassie blue staining

• Form:

  Liquid

• Buffer:

  25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

• Function:

  Transmembrane

• Molecular Weight:

  53.8 kDa

• Storage Conditions:

  Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

• Symbol:

  SLC16A1

• Species:

  Human

• Protein ID:

  NP_003042

• Overview:

  Recombinant protein of human solute carrier family 16, member 1 (monocarboxylic acid transporter 1) (SLC16A1)

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/6566

• Uniprot URL:

  https://www.uniprot.org/uniprot/P53985

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_003051

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_003042