EAAT1 rabbit pAb

EAAT1 rabbit pAb

AO-06-ES2216-50

EAAT1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES2216
Product nameEAAT1 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;ELISA
Other nameSLC1A3; EAAT1; GLAST; GLAST1; Excitatory amino acid transporter 1; Sodium-dependent glutamate/aspartate transporter 1; GLAST-1; Solute carrier family 1 member 3
Size50μL
Unit price ($)148
Human gene ID6507
Human Swiss-ProtP43003
SourceRabbit
IsotypeIgG
TargetEAAT1
Fields>>Synaptic vesicle cycle;>>Glutamatergic synapse;>>Huntington disease
Gene nameSLC1A3
Protein nameExcitatory amino acid transporter 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtP56564
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human EAAT1. AA range:492-541
SpecificityEAAT1 Polyclonal Antibody detects endogenous levels of EAAT1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. 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)65kD
BackgroundThis gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014],
Functiondisease:Defects in SLC1A3 are the cause of episodic ataxia type 6 (EA6) [MIM:612656]. EA6 is characterized by episodic ataxia, seizures, migraine and alternating hemiplegia.,function:Transports L-glutamate and also L- and D-aspartate. Essential for terminating the postsynaptic action of glutamate by rapidly removing released glutamate from the synaptic cleft. Acts as a symport by cotransporting sodium.,PTM:Glycosylated.,similarity:Belongs to the sodium:dicarboxylate (SDF) symporter (TC 2.A.23) family.,tissue specificity:Highly expressed in cerebellum, but also found in frontal cortex, hippocampus and basal ganglia.,
Subcellular locationCell membrane ; Multi-pass membrane protein .
ExpressionDetected in brain (PubMed:8218410, PubMed:7521911, PubMed:8123008). Detected at very much lower levels in heart, lung, placenta and skeletal muscle (PubMed:7521911, PubMed:8123008). Highly expressed in cerebellum, but also found in frontal cortex, hippocampus and basal ganglia (PubMed:7521911).

Additional Images

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Western Blot analysis of various cells using EAAT1 Polyclonal Antibody
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Western blot analysis of lysate from HeLa cells, using EAAT1 antibody.
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: AO-06-ES2216-50
: 10 Produits
Hurry! only 10 items left in stock.

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