SHOX2 (Human) Recombinant Protein (Q01)
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More Files
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Specification
Product Description
Human SHOX2 partial ORF ( NP_006875, 117 a.a. - 204 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
SPELKDRKDDAKGMEDEGQTKIKQRRSRTNFTLEQLNELERLFDETHYPDAFMREELSQRLGLSEARVQVWFQNRRAKCRKQENQLHK
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
35.42
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — SHOX2
Entrez GeneID
6474GeneBank Accession#
NM_006884Protein Accession#
NP_006875Gene Name
SHOX2
Gene Alias
OG12, OG12X, OGI2X, SHOT
Gene Description
short stature homeobox 2
Omim ID
602504Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
SHOX homologous gene on chromosome 3|short stature homeobox homolog
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