SHOX (NM_000451) Human Recombinant Protein
Product Specifications
Background
This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008]
Synonyms
GCFX; PHOG; SHOXY; SS
Gene ID
6473
UniProt
O15266, A0A024R385
Accession Number mRNA
NM_000451
Chromosomal Location
X; Y
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
Transcription Factors
Molecular Weight
32.1 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
SHOX
Species
Human
Protein ID
NP_000442
Overview
Recombinant protein of human short stature homeobox (SHOX), transcript variant 1
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/6473
Uniprot URL
https://www.uniprot.org/uniprot/O15266
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000451
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000442
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