SLC25A38 (NM_017875) Human Recombinant Protein

• Background:

  This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory) . A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]

• Synonyms:

  SIDBA2

• Gene ID:

  54977

• UniProt:

  Q96DW6, A1LP07

• Accession Number mRNA:

  NM_017875

• Chromosomal Location:

  3p22.1

• Expression System:

  E. coli

• Tag:

  N-His

• Concentration:

  >50 ug/mL as determined by microplate BCA method

• Purity:

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

• Form:

  Liquid

• Buffer:

  25mM Tris, pH8.0, 150 mM NaCl, 10% glycerol, 1 % Sarkosyl

• Molecular Weight:

  33.6 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:

  SLC25A38

• Species:

  Human

• Protein ID:

  NP_060345

• Overview:

  Recombinant protein of human solute carrier family 25, member 38 (SLC25A38), full length, with N-terminal HIS tag, expressed in E.Coli, 50ug

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/54977

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q96DW6

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_017875

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_060345