SKU: WP16230 Categories: ,

SHOX2 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP16230-100
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Product details

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. [provided by RefSeq, Jul 2009],

Specifications

Size50μL/100μL
TargetSHOX2
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, FC
MW(Calculated)36kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; IHC 1:50-300,Flow Cyt 1:100-200 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human SHOX2 AA range: 37-87
SpecificityThis antibody detects endogenous levels of SHOX2 at Human/Mouse/Rat
Gene NameSHOX2 OG12X SHOT
Protein NameSHOX2
Other Name
SpeciesHuman
Gene ID6474
UniprotO60902,
Species.1Mouse
Gene ID.120429
Uniprot.1P70390,
Species.2Rat
Gene ID.225546
Uniprot.2O35750
Cellular LocalizationNucleus.
Tissue ExpressionExpressed in heart, skeletal muscle, liver, lung, bone marrow fibroblast, pancreas and placenta.
Signaling_pathway
Research Areas
Functiondevelopmental stage:Expressed during cranofacial development as well as in heart.,Function:May be a growth regulator and have a role in specifying neural systems involved in processing somatosensory information, as well as in face and body structure formation.,similarity:Belongs to the paired homeobox family. Bicoid subfamily.,similarity:Contains 1 homeobox DNA-binding domain.,similarity:Contains 1 OAR domain.,tissue specificity:Expressed in heart, skeletal muscle, liver, lung, bone marrow fibroblast, pancreas and placenta.,
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