Vsx2 (NM_007701) Mouse Recombinant Protein

• Background:

  This gene encodes a member of the Vsx (visual system homeobox) family which belongs to the larger PRD homeobox class. The encoded protein is required for eye organogenesis and controls retinal development. Disruption of this gene is associated with ocular retardation J (orJ), a mouse disease which causes microphthalmia, retinal degeneration and optic nerve aplasia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]

• Synonyms:

  Chx10; Hox-1; Hox-10; Hox1; Hox10; or

• Gene ID:

  12677

• UniProt:

  Q61412, Q80WF9

• Accession Number mRNA:

  NM_007701

• Chromosomal Location:

  12 39.28 cM

• 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.

• Molecular Weight:

  39.4 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:

  Vsx2

• Species:

  Mouse

• Protein ID:

  NP_031727

• Overview:

  Purified recombinant protein of Mouse visual system homeobox 2 (Vsx2), with C-terminal MYC/DDK tag, expressed in HEK293T cells, 20ug

• Gene ID URL:

  https://www.ncbi.nlm.nih.gov/gene/12677

• Uniprot URL:

  https://www.uniprot.org/uniprot/Q61412

• Accession Number mRNA URL:

  https://www.ncbi.nlm.nih.gov/nuccore/NM_007701

• Protein ID Link:

  https://www.ncbi.nlm.nih.gov/nuccore/NP_031727