GlyRβ rabbit pAb

GlyRβ rabbit pAb

AO-06-ES5566-100

GlyRβ rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES5566
Product nameGlyRβ rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameGLRB; Glycine receptor subunit beta; Glycine receptor 58 kDa subunit
Size100μL
Unit price ($)248
Human gene ID2743
Human Swiss-ProtP48167
SourceRabbit
IsotypeIgG
TargetGlyRβ
Fields>>Neuroactive ligand-receptor interaction
Gene nameGLRB
Protein nameGlycine receptor subunit beta
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14658
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP48168
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID25456
Rat gene linkView Rat Gene
Rat Swiss-ProtP20781
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human GLRB. AA range:211-260
SpecificityGlyRβ Polyclonal Antibody detects endogenous levels of GlyRβ protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)56kD
BackgroundThis gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009],
Functiondisease:Defects in GLRB are a cause of startle disease (STHE) [MIM:149400]; also known as hereditary hyperekplexia or congenital stiff-person syndrome. STHE is a genetically heterogeneous neurologic disorder characterized by muscular rigidity of central nervous system origin, particularly in the neonatal period, and by an exaggerated startle response to unexpected acoustic or tactile stimuli. Inheritance can be autosomal dominant or recessive.,function:The glycine receptor is a neurotransmitter-gated ion channel. Binding of glycine to its receptor increases the chloride conductance and thus produces hyperpolarization (inhibition of neuronal firing).,similarity:Belongs to the ligand-gated ionic channel (TC 1.A.9) family.,subunit:Pentamer composed of alpha and beta subunits. Interacts with GPHN.,
Subcellular locationCell junction, synapse, postsynaptic cell membrane ; Multi-pass membrane protein . Cell junction, synapse . Cell projection, dendrite . Cell membrane ; Multi-pass membrane protein . Cytoplasm . Retained in the cytoplasm upon heterologous expression by itself. Coexpression with GPHN promotes expression at the cell membrane (PubMed:12684523). Coexpression with GLRA1, GLRA2 or GLRA3 promotes expression at the cell membrane. .
ExpressionBrain,Hippocampus,

Additional Images

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Western blot analysis of GLRB Antibody. The lane on the right is blocked with the GLRB peptide.
Image 2
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Western blot analysis of the lysates from HUVECcells using GLRB antibody.
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: AO-06-ES5566-100
: 10 Produits
Hurry! only 10 items left in stock.

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