PCYT1A (NM_005017) Human Recombinant Protein

• Background:

  This gene belongs to the cytidylyltransferase family and is involved in the regulation of phosphatidylcholine biosynthesis. Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]

• Synonyms:

  CCTA; CCTalpha; CT; CTA; CTPCT; PCYT1; SMDCRD

• Gene ID:

  5130

• UniProt:

  P49585

• Accession Number mRNA:

  NM_005017

• Chromosomal Location:

  3q29

• Expression System:

  HEK293T

• Tag:

  C-Myc/DDK

• Related Pathways:

  Glycerophospholipid metabolism, Metabolic pathways

• Field of Research:

  Glycerophospholipid metabolism, Metabolic pathways

• 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

• Molecular Weight:

  41.6 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:

  PCYT1A

• Species:

  Human

• Protein ID:

  NP_005008

• Overview:

  Recombinant protein of human phosphate cytidylyltransferase 1, choline, alpha (PCYT1A)

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/5130

• Uniprot URL:

  https://www.uniprot.org/uniprot/P49585

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_005017

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_005008