SKU: WP17223 Categories: ,

BTBD9 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP17223-100
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Product details

Background:

This locus encodes a BTB/POZ domain-containing protein. This domain is known to be involved in protein-protein interactions. Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011],

Specifications

Size50μL/100μL
TargetBTBD9
ReactivityHuman, Mouse, Rat
ApplicationsWB
MW(Calculated)67kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
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 BTBD9 AA range: 424-474
SpecificityThis antibody detects endogenous levels of BTBD9 at Human/Mouse/Rat
Gene NameBTBD9 KIAA1880
Protein NameBTBD9
Other Name
SpeciesHuman
Gene ID114781
UniprotQ96Q07,
Species.1Mouse
Gene ID.1224671
Uniprot.1Q8C726,
Species.2Rat
Gene ID.2294318
Uniprot.2Q5PQR3
Cellular Localizationcytoplasm,SCF ubiquitin ligase complex,
Tissue ExpressionDetected in the brain (at protein level) (PubMed:22658601). Moderately expressed in all specific brain regions examined (PubMed:11572484). Expressed in the dopaminergic neurons of the substantia nigra and A11 neurons (PubMed:22658601). Highly expressed in kidney and moderately expressed in all other adult and fetal tissues (PubMed:11572484).
Signaling_pathway
Research Areas
FunctionDisease:Genetic variations in BTBD9 are associated with susceptibility to restless legs syndrome type 6 (RLS6) [MIM:611185]; also called periodic limb movements in sleep. Restless legs syndrome (RLS) is a neurologic disorder characterized by an uncontrollable urge to move the legs during periods of rest. The majority of patients with RLS also have periodic limb movements in sleep, which are characterized by involuntary, highly stereotypical, regularly occurring limb movements that occur during sleep.,similarity:Contains 1 BACK (BTB/Kelch associated) domain.,similarity:Contains 1 BTB (POZ) domain.,tissue specificity:Highly expressed in kidney and moderately expressed in all other adult and fetal tissues. Moderately expressed in all specific brain regions examined.,
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