"SHOX" Related Products

Recombinant Human SHOX cell lysate

Cat.No.: SHOX-1603HCL
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.
Species: Human
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 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;

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