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EAAT2 antibody extracellular domain - 250 211

EAATs are transmembrane proteins involved in the removal of extracellular glutamate
Mouse monoclonal purified IgG
Cat. No.: 250 211
Amount: 100 µg
Price: $415.00
Cat. No. 250 211 100 µg purified IgG, lyophilized. Albumin and azide were added for stabilization. For reconstitution add 100 µl H2O to get a 1mg/ml solution in PBS. Then aliquot and store at -20°C to -80°C until use.
Antibodies should be stored at +4°C when still lyophilized. Do not freeze!
Applications
 
WB: 1 : 1000 up to 1 : 5000 (AP-staining) gallery  
IP: not tested yet
ICC: 1 : 500 up to 1 : 1000 gallery  
IHC: 1 : 500 gallery  
IHC-P: 1 : 200 up to 1 : 1000 gallery  
Clone SY-4E7
Subtype IgG2b (κ light chain)
Immunogen Synthetic peptide corresponding to residues surrounding AA 150 of mouse EAAT2 (UniProt Id: P43006)
Reactivity Reacts with: mouse (P43006), rat (P31596).
Other species not tested yet.
Matching control protein/peptide 250-2P
Data sheet 250_211.pdf
Cat. No.: 250 211
Amount: 100 µg
Price: $415.00
Background

Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system. After the release of glutamate from synaptic vesicles into the synaptic cleft during neurotransmission, excitatory amino acid transporters (EAATs) remove extracellular glutamate to avoid excitotoxic levels (1).
Five EAATs with differential expression patterns have been described so far: EAAT1, also referred to as GLAST and SLC1A3, has neuroprotective potential following ischemia and occurs in reactive astrocytes and activated microglia. EAAT2 (GLT-1, SLC1A2) is the most abundant isoform and is primarily expressed in astrocytes. Both variants show high levels in brain and retina. EAAT3 / SLC1A1, EAAT4 / SLC1A6 and EAAT5 / SLC1A7 are expressed in neurons (2). EAAT4 shows weak expression in the forebrain and high levels in the cerebellum, where it mainly locates to Purkinje cells (3). EAAT5 primarily occurs in the retina, where it locates very close to glutamate release sites. In K.O. mice flicker resolution is considerably compromised (4). Recent findings suggest that EAAT5 is an abundant isoform, expressed also in non-neuronal peripheral tissues (5).