SHOX2 purified MaxPab mouse polyclonal antibody (B01P)
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More Files
- More Functions
Western Blot (Transfected lysate)
Western Blot analysis of SHOX2 expression in transfected 293T cell line (H00006474-T01) by SHOX2 MaxPab polyclonal antibody.
Lane 1: SHOX2 transfected lysate(39.05 KDa).
Lane 2: Non-transfected lysate.
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human SHOX2 protein.
Immunogen
SHOX2 (AAH08829.1, 1 a.a. ~ 355 a.a) full-length human protein.
Sequence
MEELTAFVSKSFDQKVKEKKEAITYREVLESGPLRGAKEPTGCTEAGRDDRSSPAVRAAGGGGGGGGGGGGGGGGGGVGGGGAGGGAGGGRSPVRELDMGAAERSREPGSPRLTEGRRKPTKAEVQATLLLPGEAFRFLVSPELKDRKEDAKGMEDEGQTKIKQRRSRTNFTLEQLNELERLFDETHYPDAFMREELSQRLGLSEARVQVWFQNRRAKCRKQENQLHKGVLIGAASQFEACRVAPYVNVGALRMPFQQDSHCNVTPLSFQVQAQLQLDSAVAHAHHHLHPHLAAHAPYMMFPAPPFGLPLATLAADSASAASVVAAAAAAKTTSKNSSIADLRLKAKKHAAALGL
Host
Mouse
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of SHOX2 expression in transfected 293T cell line (H00006474-T01) by SHOX2 MaxPab polyclonal antibody.
Lane 1: SHOX2 transfected lysate(39.05 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — SHOX2
Entrez GeneID
6474GeneBank Accession#
BC008829.2Protein Accession#
AAH08829.1Gene 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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