SHOX2 antibody (clone 1D1), anti-human, rat
€435.00
In stock
SKU
AC-AT3885a
Catalog Number: AC-AT3885a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, Ehttps://www.abcepta.com/products/pdf_download/AT3885a-SHOX2-Antibody-monoclonal-M01">Request Information AC-AT3885a">Request Information
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, Ehttps://www.abcepta.com/products/pdf_download/AT3885a-SHOX2-Antibody-monoclonal-M01">Request Information AC-AT3885a">Request Information
Background:
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.
Other Names:
Short stature homeobox protein 2, Homeobox protein Og12X, Paired-related homeobox protein SHOT, SHOX2, OG12X, SHOT
Antigen Type:
Recombinant Protein
Gene Name: SHOX2
Gene ID: 6474
NCBI Accession: NP_001157150.1;NP_003021.3;NP_006875.2
Primary Accession: O60902
Other Accession: NM_006884
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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.
Other Names:
Short stature homeobox protein 2, Homeobox protein Og12X, Paired-related homeobox protein SHOT, SHOX2, OG12X, SHOT
Antigen Type:
Recombinant Protein
Gene Name: SHOX2
Gene ID: 6474
NCBI Accession: NP_001157150.1;NP_003021.3;NP_006875.2
Primary Accession: O60902
Other Accession: NM_006884
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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