Vsx2 (NM_007701) Mouse Recombinant Protein
Product Specifications
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
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