TXNL6 (NXNL1) (NM_138454) Human Recombinant Protein

• Background:

  Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP. [provided by RefSeq, Dec 2015]

• Synonyms:

  RDCVF; TXNL6

• Gene ID:

  115861

• UniProt:

  Q96CM4

• Accession Number mRNA:

  NM_138454

• Chromosomal Location:

  19p13.11

• 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:

  Druggable Genome

• Molecular Weight:

  23.8 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:

  NXNL1

• Species:

  Human

• Protein ID:

  NP_612463

• Overview:

  Recombinant protein of human nucleoredoxin-like 1 (NXNL1)

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/115861

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q96CM4

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_138454

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_612463