Recombinant Human SHOX cell lysate

• Cat.No.: SHOX-1603HCL

Specification

• Species: Human
• Tag: Non
• Description: 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.
• Size: 100 ul
• Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
• Applications: Western Blot

Gene Information

• Gene Name: SHOX short stature homeobox [ Homo sapiens ]
• Official Symbol: SHOX
• Synonyms: SHOX; short stature homeobox; short stature homeobox protein; GCFX; PHOG; SHOXY; SS; growth control factor, X-linked; short stature homeobox-containing protein; pseudoautosomal homeobox-containing osteogenic protein
• Gene ID: 6473
• mRNA Refseq: NM_000451
• Protein Refseq: NP_000442
• MIM: 312865
• UniProt ID: O15266
• Chromosome Location: Xp22.33 and Yp11.32
• Function: protein binding; sequence-specific DNA binding transcription factor activity; transcription regulatory region sequence-specific DNA binding