Lebercilin (LCA5) (NM_001122769) Human Recombinant Protein

• Background:

  This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]

• Synonyms:

  C6orf152

• Gene ID:

  167691

• UniProt:

  Q86VQ0, A0A384MDJ7

• Accession Number mRNA:

  NM_001122769

• Chromosomal Location:

  6q14.1

• 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, 150mM NaCl, 10% glycerol, 1 % Sarkosyl.

• Molecular Weight:

  80.4 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:

  LCA5

• Species:

  Human

• Protein ID:

  NP_001116241

• Overview:

  Purified recombinant protein of Human Leber congenital amaurosis 5 (LCA5), transcript variant 2, full length, with N-terminal HIS tag, expressed in E. coli, 50ug

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/167691

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q86VQ0

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_001122769

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_001116241