EAAT2/GLT1 Antibodies
We offer EAAT2/GLT1 Antibodies for use in common research applications: ELISA, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, In vivo assay, Sandwich ELISA, Western Blot. Each EAAT2/GLT1 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our EAAT2/GLT1 Antibodies can be used in a variety of model species: Human, Mouse, Rat. Use the list below to choose the EAAT2/GLT1 Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our EAAT2/GLT1 polyclonal antibodies and browse our EAAT2/GLT1 monoclonal antibody catalog.
Alternate Names for EAAT2/GLT1 Antibodies
anti-EAAT2/GLT1 antibody, anti-SLC1A2 antibody, anti-GLT1 antibody, anti-member 2 antibody, anti-solute carrier family 1 (glial high affinity glutamate transporter), member 2 antibody, anti-Solute carrier family 1 member 2 antibody
11 Results for "eaat2-glt1" in Primary Antibodies
![Western Blot: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Blocking: 1% LFDM for 30 min at RT; primary antibody: dilution 1:1000 incubated overnight at 4C.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Western-Blot-NBP1-20136-img0002.jpg "Western Blot: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Blocking: 1% LFDM for 30 min at RT; primary antibody: dilution 1:1000 incubated overnight at 4C.")
![Immunocytochemistry/Immunofluorescence: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Human NPCs differentiate into mature neurons. Immunofluorescence staining of differentiated neurons derived from human dorsal NPCs (1323-2 line, day 35 after differentiation) for mature cortical neuronal markers expressed in the nucleus (BRN2, TBR1, NeuN) and cytoplasm (MAP2), glial markers (SOX9, GFAP, GLT1), and dorsal forebrain marker (FOXG1). Nuclei stained with DAPI, shown as an overlay over brightfield images. The merge is an overlay of the neuronal and glial markers. Scale bar 100 um. DAPI 4,6'-diamino-2-phenylindole Image collected and cropped by CiteAb from the following publication (//stemcellres.biomedcentral.com/articles/10.1186/s13287-018-0812-6) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunocytochemistry-Immunofluorescence-NBP1-20136-img0015.jpg)
![Immunohistochemistry: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Hippocampal GLT-1 and NR1 expression 3 days after SE with MyD88 inhibition. Sections from the hippocampi of mice in the CP group (A1-A3) and MIP group (B1-B3) 3 days after SE with GLT-1 immunoreactivity in astrocytes and neuronal processes. (A4, B4) Higher magnification of the boxes in (A3) and (B3). Scale bars: (A1-A3, B1-B3) 100 um; (A4, B4) 50 um. SE = status epilepticus, DG=dentate gyrus, hippocampal regions CA3 and CA1, CP = control peptide, MIP = MyD88 inhibitory peptide. Image collected and cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/30112701/) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/EAAT2-GLT1 Antibody - Azide Free-Immunohistochemistry-NBP1-20136-img0016.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse spinal cord. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0003.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse spinal cord. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0004.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse olfactory bulbs. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0005.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse brain (hippocampus). The animal was perfused at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0006.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse brain (hippocampus). The animal was perfused at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0007.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse brain (hippocampus). The animal was perfused at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0008.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse olfactory bulbs. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0009.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Mouse brain (hippocampus). The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0010.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Sections of mouse spinal cord. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0011.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Sections of mouse spinal cord. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0012.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Sections of mouse olfactory bulbs. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0013.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody - Azide Free [NBP1-20136] - Sections of mouse olfactory bulbs. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody---Azide-Free-Immunohistochemistry-Paraffin-NBP1-20136-img0014.jpg)
![Western Blot: EAAT2/GLT1 Antibody [NBP1-59632] - Fetal Brain Lane A: Primary Antibody Lane B:Primary Antibody + Blocking Peptide Primary Antibody Concentration:1ug/ml Peptide Concentration: 5ug/ml Lysate Quantity: 25ug/lane/Lane Gel Concentration: 0.12](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Western-Blot-NBP1-59632-img0015.jpg "Western Blot: EAAT2/GLT1 Antibody [NBP1-59632] - Fetal Brain Lane A: Primary Antibody Lane B:Primary Antibody + Blocking Peptide Primary Antibody Concentration:1ug/ml Peptide Concentration: 5ug/ml Lysate Quantity: 25ug/lane/Lane Gel Concentration: 0.12")
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-59632] - Human alveolar cell.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-59632-img0011.jpg)
![Western Blot: EAAT2/GLT1 Antibody [NBP1-59632] - Titration: 0.2-1 ug/ml, Positive Control: Human brain.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Western-Blot-NBP1-59632-img0012.jpg)
![Western Blot: EAAT2/GLT1 Antibody [NBP1-59632] - WB analysis of GLT1 in Hep3B WCL. Image courtesy of anonymous customer product review.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Western-Blot-NBP1-59632-img0013.jpg)
![Western Blot: EAAT2/GLT1 Antibody [NBP1-59632] - Human Fetal Brain lysates.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Western-Blot-NBP1-59632-img0014.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-59632] - Human Brain, cortex tissue at an antibody concentration of 5 ug/ml.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-59632-img0010.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-84027] - Analysis in human cerebral cortex and fallopian tube tissues using NBP1-84027 antibody. Corresponding EAAT2/GLT1 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-84027-img0007.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-84027] - Analysis in human cerebral cortex and fallopian tube tissues using NBP1-84027 antibody. Corresponding EAAT2/GLT1 RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-84027] - Staining of human lymph node shows no positivity in non-germinal center cells as expected.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-84027-img0011.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-84027] - Staining of human cerebral cortex shows high expression.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-84027-img0004.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-84027] - Staining of human placenta shows no positivity in trophoblastic cells as expected.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-84027-img0009.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-84027] - Staining of human placenta shows no positivity in trophoblastic cells as expected.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-84027-img0010.jpg)
![Western Blot: EAAT2/GLT1 Antibody [NBP3-13348] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EAAT2/GLT1 antibody (NBP3-13348) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Western-Blot-NBP3-13348-img0001.jpg "Western Blot: EAAT2/GLT1 Antibody [NBP3-13348] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EAAT2/GLT1 antibody (NBP3-13348) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP3-13348] - EAAT2/GLT1 antibody detects EAAT2/GLT1 protein at cell membrane by immunohistochemical analysis. Sample: Paraffin-embedded mouse hippocampus. EAAT2/GLT1 stained by EAAT2/GLT1 antibody (NBP3-13348) diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP3-13348-img0003.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP3-13348] - EAAT2/GLT1 antibody detects EAAT2/GLT1 protein at cell membrane by immunohistochemical analysis. Sample: Paraffin-embedded mouse eye. Green: EAAT2/GLT1 stained by EAAT2/GLT1 antibody (NBP3-13348) diluted at 1:250. Red: beta Tubulin 3/ Tuj1, a cytoplasm marker, stained by beta Tubulin 3/ Tuj1 antibody [GT1338] (NBP3-13505) diluted at 1:500. Blue: Fluoroshield with DAPI. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP3-13348-img0002.jpg)
![Western Blot: EAAT2/GLT1 Antibody (PS01-62) [NBP3-32287] - Western blot analysis of EAAT2/GLT1 on different lysates with Rabbit anti-EAAT2/GLT1 antibody (NBP3-32287) at 1/1,000 dilution. Lane 1: Mouse brain tissue lysate (20 ug/Lane) Lane 2: Rat brain tissue lysate (20 ug/Lane) Lane 3: Mouse cerebellum tissue lysate (20 ug/Lane) Predicted band size: 62 kDa Observed band size: 62 kDa Exposure time: 2 minutes; 8% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32287) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32287_rabbit-eaat2-glt1-mab-ps01-62-278202415242637.jpg "Western Blot: EAAT2/GLT1 Antibody (PS01-62) [NBP3-32287] - Western blot analysis of EAAT2/GLT1 on different lysates with Rabbit anti-EAAT2/GLT1 antibody (NBP3-32287) at 1/1,000 dilution. Lane 1: Mouse brain tissue lysate (20 ug/Lane) Lane 2: Rat brain tissue lysate (20 ug/Lane) Lane 3: Mouse cerebellum tissue lysate (20 ug/Lane) Predicted band size: 62 kDa Observed band size: 62 kDa Exposure time: 2 minutes; 8% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32287) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: EAAT2/GLT1 Antibody (PS01-62) [NBP3-32287] - Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-EAAT2/GLT1 antibody (NBP3-32287) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32287) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32287_rabbit-eaat2-glt1-mab-ps01-62-29820241435275.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP3-17032] - Staining of human cerebral cortex shows high expression.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP3-17032-img0002.jpg "Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP3-17032] - Staining of human cerebral cortex shows high expression.")
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP3-17032] - Analysis in human cerebral cortex and small intestine tissues using Anti-SLC1A2 antibody. Corresponding SLC1A2 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP3-17032-img0001.jpg)
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP3-17032] - Staining of human small intestine shows low expression as expected.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP3-17032-img0003.jpg)
![Western Blot: EAAT2/GLT1 Antibody [NBP1-59633] - HT1080 cell lysate, Antibody Titration: 0.2-1 ug/ml](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Western-Blot-NBP1-59633-img0001.jpg "Western Blot: EAAT2/GLT1 Antibody [NBP1-59633] - HT1080 cell lysate, Antibody Titration: 0.2-1 ug/ml")
![Immunohistochemistry-Paraffin: EAAT2/GLT1 Antibody [NBP1-59633] - Human Brain, cortex tissue at an antibody concentration of 5 ug/ml.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-Immunohistochemistry-Paraffin-NBP1-59633-img0003.jpg)
![Western Blot: EAAT2/GLT1 Antibody (28F9) [NBP3-26322] - Positive Western Blot detected in: U251 whole cell lysate. All lanes: EAAT2/GLT1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 62 kDa Observed band size: 62 kDa](http://images.novusbio.com/fullsize/nbp3-26322_rabbit-eaat2-glt1-mab-28f9-28220241140946.jpg "Western Blot: EAAT2/GLT1 Antibody (28F9) [NBP3-26322] - Positive Western Blot detected in: U251 whole cell lysate. All lanes: EAAT2/GLT1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 62 kDa Observed band size: 62 kDa")
![Flow Cytometry: EAAT2/GLT1 Antibody (28F9) [NBP3-26322] - Overlay Peak curve showing MCF-7 cells stained with EAAT2/GLT1 Antibody (28F9) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26322_rabbit-eaat2-glt1-mab-28f9-282202414183678.jpg)
![Western Blot: EAAT2/GLT1 Antibody (SR2082) [NBP3-21735] - Western blot analysis using NBP3-21735 in HeLa cell lysate.](http://images.novusbio.com/fullsize/nbp3-21735_rabbit-eaat2-glt1-mab-sr2082-5720231784614.jpg "Western Blot: EAAT2/GLT1 Antibody (SR2082) [NBP3-21735] - Western blot analysis using NBP3-21735 in HeLa cell lysate.")
![Western Blot: EAAT2/GLT1 Antibody (1D8) [H00006506-M07] - Analysis of SLC1A2 expression in HeLa (Cat # L013V1).](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-1D8-Western-Blot-H00006506-M07-img0003.jpg "Western Blot: EAAT2/GLT1 Antibody (1D8) [H00006506-M07] - Analysis of SLC1A2 expression in HeLa (Cat # L013V1).")
![ELISA: EAAT2/GLT1 Antibody (1D8) [H00006506-M07] - Detection limit for recombinant GST tagged SLC1A2 is approximately 0.03ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-1D8-ELISA-H00006506-M07-img0002.jpg)
![ELISA: EAAT2/GLT1 Antibody (4G8) [H00006506-M10] - Detection limit for recombinant GST tagged SLC1A2 is approximately 0.3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/EAAT2-GLT1-Antibody-4G8-ELISA-H00006506-M10-img0001.jpg "ELISA: EAAT2/GLT1 Antibody (4G8) [H00006506-M10] - Detection limit for recombinant GST tagged SLC1A2 is approximately 0.3ng/ml as a capture antibody.")