"SHOX2" Related Products

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Recombinant Human SHOX2 cell lysate

Cat.No.: SHOX2-1604HCL
Description: This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
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: SHOX2 short stature homeobox 2 [ Homo sapiens ]
Official Symbol: SHOX2
Synonyms: SHOX2; short stature homeobox 2; short stature homeobox protein 2; OG12; OG12X; SHOT; homeobox protein Og12X; SHOX homologous gene on chromosome 3; paired-related homeobox protein SHOT;
Gene ID: 6474
mRNA Refseq: NM_001163678
Protein Refseq: NP_001157150
MIM: 602504
UniProt ID: O60902
Chromosome Location: 3q25.32
Function: transcription regulatory region sequence-specific DNA binding;

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