SKU: WP17134 Categories: ,

SPTN2 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP17134-100
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Product details

Background:

Spectrins are principle components of a cell's membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits. The protein encoded by this gene (SPTBN2), is called spectrin beta non-erythrocytic 2 or beta-III spectrin. It is related to, but distinct from, the beta-II spectrin gene which is also known as spectrin beta non-erythrocytic 1 (SPTBN1). SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the surface of the plasma membrane. Mutations in this gene cause a form of spinocerebellar ataxia, SCA5, that is characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements. [provided by RefSeq, Dec 2009],

Specifications

Size50μL/100μL
TargetSPTN2
ReactivityHuman, Rat
ApplicationsWB, IHC
MW(Calculated)263kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; IHC 1:50-300 / 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 SPTN2 AA range: 644-694
SpecificityThis antibody detects endogenous levels of SPTN2 at Human/Rat
Gene NameSPTBN2 KIAA0302 SCA5
Protein NameSPTN2
Other Name
SpeciesHuman
Gene ID6712
UniprotO15020,
Species.1
Gene ID.1
Uniprot.1
Species.2Rat
Gene ID.229211
Uniprot.2Q9QWN8
Cellular LocalizationCytoplasm, cytoskeleton. Cytoplasm, cell cortex.
Tissue ExpressionHighly expressed in brain, kidney, pancreas, and liver, and at lower levels in lung and placenta.
Signaling_pathwayHuman Diseases >> Neurodegenerative disease >> Spinocerebellar ataxia;Human Diseases >> Neurodegenerative disease >> Pathways of neurodegeneration - multiple diseases
Research Areas>>Spinocerebellar ataxia; / >>Pathways of neurodegeneration - multiple diseases
FunctionDisease:Defects in SPTBN2 are the cause of spinocerebellar ataxia type 5 (SCA5) [MIM:600224]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA5 is an autosomal dominant cerebellar ataxia (ADCA). It is a slowly progressive disorder with variable age at onset, ranging between 10 and 50 years.,Function:Probably plays an important role in neuronal membrane skeleton.,similarity:Belongs to the spectrin family.,similarity:Contains 1 PH domain.,similarity:Contains 17 spectrin repeats.,similarity:Contains 2 CH (calponin-homology) domains.,tissue specificity:Highly expressed in brain, kidney, pancreas, and liver, and at lower levels in lung and placenta.,
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