| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-43789 | |||
| BSA Free | NBP2-46641-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-71097 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-72948 | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Atto594 | NBP3-14765-100ug | |||
![Western Blot: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Analysis of p75 NGF Receptor on PC-12 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Western-Blot-NBP2-67296-img0011.jpg "Western Blot: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Analysis of p75 NGF Receptor on PC-12 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA 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.")
![Immunocytochemistry/Immunofluorescence: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Staining NGFR p75 in N2A cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunocytochemistry-Immunofluorescence-NBP2-67296-img0005.jpg)
![Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Rat uterus tissue using anti-p75 NGF Receptor antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0009.jpg)
![Western Blot: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Western blot analysis of NGFR/TNFRSF16/p75NTR on skeletal muscle tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperatur](http://images.novusbio.com/fullsize/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Western-Blot-NBP2-67296-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Staining NGFR p75 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunocytochemistry-Immunofluorescence-NBP2-67296-img0001.jpg)
![Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Analysis of mouse uterus tissue using anti-p75 NGF Receptor antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0006.jpg)
![Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Human tonsil tissue using anti-p75 NGF Receptor antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0007.jpg)
![Immunohistochemistry-Paraffin: NGFR/TNFRSF16/p75NTR Antibody (SA39-02) [NBP2-67296] - Human uterus tissue using anti-p75 NGF Receptor antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes 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/NGFR-TNFRSF16-p75NTR-Antibody-SA39-02-Immunohistochemistry-Paraffin-NBP2-67296-img0008.jpg)
![Immunohistochemistry-Paraffin: NGF R/TNFRSF16/p75NTR Antibody [NBP2-19669] - Rat brain. p75 NGF Receptor antibody diluted at 1:500.](http://images.novusbio.com/fullsize/NGF-R-TNFRSF16-p75NTR-Antibody-Immunohistochemistry-Paraffin-NBP2-19669-img0005.jpg "Immunohistochemistry-Paraffin: NGF R/TNFRSF16/p75NTR Antibody [NBP2-19669] - Rat brain. p75 NGF Receptor antibody diluted at 1:500.")
![Western Blot: NGFR/TNFRSF16/p75NTR Antibody [NBP2-19669] - Untreated (-) and treated (+) PC-3 whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with NGFR/TNFRSF16/p75NTR antibody (NBP2-19669) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-19669_rabbit-polyclonal-ngfr-tnfrsf16-p75ntr-antibody-91020242063324.jpg)
![p75 NGF Receptor / CD271 antibody detects p75 NGF Receptor / CD271 protein by immunofluorescent analysis.Sample: DIV10 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: p75 NGF Receptor / CD271 stained by p75 NGF Receptor / CD271 antibody (NBP2-19669) diluted at 1:500.Red: Tau, stained by Tau antibody [GT287] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp2-19669_rabbit-polyclonal-ngfr-tnfrsf16-p75ntr-antibody-immunocytochemistry-immunofluorescence-261120251823614.jpg)
![p75 NGF Receptor antibody detects p75 NGF Receptor protein expression by immunohistochemical analysis.Sample: Frozen sectioned E13.5 Rat brain. Green: p75 NGF Receptor protein stained by p75 NGF Receptor antibody (NBP2-19669) diluted at 1:250.Red: beta Tubulin 3/ TUJ1, a mature neuron marker, stained by beta Tubulin 3/ TUJ1 antibody [GT11710] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp2-19669_rabbit-polyclonal-ngfr-tnfrsf16-p75ntr-antibody-immunohistochemistry-frozen-2611202518303814.jpg)
![Western Blot: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with AChE antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Western-Blot-NBP1-31329-img0020.jpg "Western Blot: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with AChE antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Mouse brain. AChE stained by AChE antibody diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Immunohistochemistry-Paraffin-NBP1-31329-img0021.jpg)
![Western Blot: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Sample (30 ug of whole cell lysate) A: Raji 7. 5% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Western-Blot-NBP1-31329-img0009.jpg)
![Western Blot: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with AChE antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Western-Blot-NBP1-31329-img0014.jpg)
![Western Blot: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Rat tissue extract (50 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with AChE antibody diluted at 1:500.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Western-Blot-NBP1-31329-img0018.jpg)
![Immunocytochemistry/Immunofluorescence: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Paraformaldehyde-fixed HeLa, using AChE antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with an alpha Tubulin antibody (Red) at 1:2500.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-31329-img0008.jpg)
![Immunohistochemistry-Paraffin: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Mouse colon. AChE antibody dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Immunohistochemistry-Paraffin-NBP1-31329-img0010.jpg)
![Immunohistochemistry-Paraffin: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Rat fore brain. AChE antibody dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Immunohistochemistry-Paraffin-NBP1-31329-img0011.jpg)
![Immunohistochemistry-Paraffin: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Rat brain. AChE antibody diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/Acetylcholinesterase-ACHE-Antibody-Immunohistochemistry-Paraffin-NBP1-31329-img0012.jpg)
![Immunohistochemistry-Paraffin: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Acetylcholinesterase/ACHE antibody detects Acetylcholinesterase/ACHE protein at nucleus by immunohistochemical analysis.Sample: Paraffin-embedded mouse brain.Acetylcholinesterase/ACHE stained by Acetylcholinesterase/ACHE antibody (NBP1-31329) diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp1-31329_rabbit-polyclonal-acetylcholinesterase-ache-antibody-91020242091450.jpg)
![Western Blot: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Human tissue extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with Acetylcholinesterase/ACHE antibody (NBP1-31329) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp1-31329_rabbit-polyclonal-acetylcholinesterase-ache-antibody-910202420104428.jpg)
![Immunohistochemistry-Paraffin: Acetylcholinesterase/ACHE Antibody [NBP1-31329] - Acetylcholinesterase/ACHE antibody detects Acetylcholinesterase/ACHE protein at nucleus by immunohistochemical analysis.Sample: Paraffin-embedded rat brain.Acetylcholinesterase/ACHE stained by Acetylcholinesterase/ACHE antibody (NBP1-31329) diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp1-31329_rabbit-polyclonal-acetylcholinesterase-ache-antibody-91020242001048.jpg)
![Acetylcholinesterase/ACHE antibody detects Acetylcholinesterase/ACHE protein by immunofluorescent analysis.Sample: DIV9 rat hippocampal neuron and Glia cell cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: Acetylcholinesterase/ACHE stained by Acetylcholinesterase/ACHE antibody (NBP1-31329) diluted at 1:500.Red: Tau, an axon marker, stained by Tau antibody [GT287] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp1-31329_rabbit-polyclonal-acetylcholinesterase-ache-antibody-immunocytochemistry-immunofluorescence-1411202518443420.jpg)
![Acetylcholinesterase/ACHE antibody detects Acetylcholinesterase/ACHE protein expression by immunohistochemical analysis.Sample: Frozen sectioned E13.5 Rat brain. Green: Acetylcholinesterase/ACHE protein stained by Acetylcholinesterase/ACHE antibody (NBP1-31329) diluted at 1:250.Red: beta Tubulin 3/ TUJ1, a mature neuron marker, stained by beta Tubulin 3/ TUJ1 antibody [GT11710] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-48812_rabbit-opsin-1-medium-wave-mab-hl3435-immunohistochemistry-frozen-14112025185548.jpg)
![Western Blot: VAChT/SLC18A3 Antibody [NB100-91348] - Rat and mouse tissue lysates. Blocking: 1% LFDM for 30 min at RT; primary antibody: dilution 1:2000 incubated at 4C overnight.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Western-Blot-NB100-91348-img0032.jpg "Western Blot: VAChT/SLC18A3 Antibody [NB100-91348] - Rat and mouse tissue lysates. Blocking: 1% LFDM for 30 min at RT; primary antibody: dilution 1:2000 incubated at 4C overnight.")
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - Rat spinal cord. 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. Blocking: 0.2% LFDM in TBST filtered thru 0.2 um.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0031.jpg)
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - IHC on rat spinal cord (paraffin section) using Rabbit antibody to (Vesicular Acetylcholine Transporter) VACHT: whole serum at 1 : 200 dilution incubated overnight at 4C, developed with DAB/Ni and counterstained with hematoxylin.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0015.jpg)
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - IHC on rat spinal cord (paraffin section) using Rabbit antibody to (Vesicular Acetylcholine Transporter) VACHT: whole serum at 1 : 200 dilution incubated overnight at 4C, developed with DAB/Ni and counterstained with hematoxylin.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0016.jpg)
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - IHC on rat spinal cord (paraffin section) using Rabbit antibody to (Vesicular Acetylcholine Transporter) VACHT: whole serum at 1 : 200 dilution incubated overnight at 4C, developed with DAB/Ni and counterstained with hematoxylin.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0018.jpg)
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - IHC on rat spinal cord (paraffin section) using Rabbit antibody to (Vesicular Acetylcholine Transporter) VACHT: whole serum at 1 : 200 dilution incubated overnight at 4C, developed with DAB/Ni and counterstained with hematoxylin.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0026.jpg)
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - IHC on rat spinal cord (paraffin section) using Rabbit antibody to (Vesicular Acetylcholine Transporter) VACHT: whole serum at 1 : 200 dilution incubated overnight at 4C, developed with DAB/Ni and counterstained with hematoxylin.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0028.jpg)
![Immunohistochemistry-Paraffin: VAChT/SLC18A3 Antibody [NB100-91348] - IHC on rat spinal cord (paraffin section) using Rabbit antibody to (Vesicular Acetylcholine Transporter) VACHT: whole serum at 1 : 200 dilution incubated overnight at 4C, developed with DAB/Ni and counterstained with hematoxylin.](http://images.novusbio.com/fullsize/VAChT-SLC18A3-Antibody-Immunohistochemistry-Paraffin-NB100-91348-img0029.jpg)
![Western Blot: VGLUT1 Antibody [NBP3-13165] - Human tissue extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with VGluT1 antibody 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/VGLUT1-Antibody-Western-Blot-NBP3-13165-img0013.jpg "Western Blot: VGLUT1 Antibody [NBP3-13165] - Human tissue extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with VGluT1 antibody diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: VGLUT1 Antibody [NBP3-13165] - VGLUT1 antibody detects VGLUT1 protein by immunofluorescent analysis. Sample: DIV10 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: VGLUT1 stained by VGLUT1 antibody (NBP3-13165) diluted at 1:500. Red: Tau, stained by Tau antibody [GT287] diluted at 1:500. Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/VGLUT1-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13165-img0005.jpg)
![Immunohistochemistry-Frozen: VGLUT1 Antibody [NBP3-13165] - VGLUT1 antibody detects VGLUT1 protein expression by immunohistochemical analysis. Sample: Frozen-sectioned adult mouse cerebellum. Green: VGLUT1 protein stained by VGLUT1 antibody (NBP3-13165) diluted at 1:250. Red: beta Tubulin 3/ TUJ1, stained by beta Tubulin 3/ TUJ1 antibody [11710] (NBP2-43559) diluted at 1:500. Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/VGLUT1-Antibody-Immunohistochemistry-Frozen-NBP3-13165-img0002.jpg)
![Immunohistochemistry-Paraffin: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein by immunohistochemical analysis. Sample: Paraffin-embedded mouse eye. Green: VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:100. Red: beta Tubulin 3/ Tuj1, a Cytoskeleton marker, stained by beta Tubulin 3/ Tuj1 antibody [GT11710] (NBP2-43559) diluted at 1:500. Blue: Fluoroshield with DAPI . Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-212024938316.jpg "Immunohistochemistry-Paraffin: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein by immunohistochemical analysis. Sample: Paraffin-embedded mouse eye. Green: VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:100. Red: beta Tubulin 3/ Tuj1, a Cytoskeleton marker, stained by beta Tubulin 3/ Tuj1 antibody [GT11710] (NBP2-43559) diluted at 1:500. Blue: Fluoroshield with DAPI . Antigen Retrieval: Citrate buffer, pH 6.0, 15 min")
![Immunohistochemistry-Paraffin: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein by immunohistochemical analysis. Sample: Paraffin-embedded mouse brain. Green: VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:100. Red: NF-H, a Cytoplasm marker, stained by NF-H antibody [GT114] diluted at 1:500. Blue: Fluoroshield with DAPI . Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249425448.jpg)
![Immunocytochemistry/Immunofluorescence: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein at nucleus and cytoskeleton by immunofluorescent analysis. Sample: DIV9 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:250. Red: Tau, an axon marker, stained by Tau antibody [GT287] diluted at 1:500. Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249362775.jpg)
![Immunohistochemistry-Frozen: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein at cell membrane by immunohistochemical analysis. Sample: Frozen-sectioned mouse cerebellum. Green: VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:100. Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249415958.jpg)
![Western Blot: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - Non-transfected (-) and transfected (+) Boiled and unboiled 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with VGAT antibody [HL1616] (NBP3-25743) diluted at 1:50000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249415994.jpg)
![Immunohistochemistry-Frozen: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein by immunohistochemical analysis. Sample: Frozen-sectioned mouse cerebellum. Green: VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:100.](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249422680.jpg)
![Immunohistochemistry-Paraffin: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - VGAT antibody [HL1616] detects VGAT protein at cytoplasm by immunohistochemical analysis. Sample: Paraffin-embedded mouse cerebellum. VGAT stained by VGAT antibody [HL1616] (NBP3-25743) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249362722.jpg)
![Western Blot: VIAAT/SLC32A1/VGAT Antibody (HL1616) - Azide and BSA Free [NBP3-25743] - Boiled and unboiled mouse tissue extract (50 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with VGAT antibody [HL1616] (NBP3-25743) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-2120249403895.jpg)
![Non-transfected (-) and transfected (+) unboiled 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with VIAAT/SLC32A1/VGAT antibody [HL1615] (NBP3-25743) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25743_rabbit-viaat-slc32a1-vgat-mab-hl1616-azide-and-bsa-free-western-blot-141120251832021.jpg)
![Immunohistochemistry-Paraffin: VGLUT2 Antibody (CL2952) [NBP2-46641] - Analysis in human cerebral cortex and tonsil tissues using NBP2-46641 antibody. Corresponding VGLUT2 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-Paraffin-NBP2-46641-img0015.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: VGLUT2 Antibody (CL2952) [NBP2-46641] - Analysis in human cerebral cortex and tonsil tissues using NBP2-46641 antibody. Corresponding VGLUT2 RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: VGLUT2 Antibody (CL2952) [NBP2-46641] - Staining of human kidney shows absence of immunoreactivity (negative control).](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-Paraffin-NBP2-46641-img0008.jpg)
![Immunohistochemistry: VGLUT2 Antibody (CL2952) [NBP2-46641] - VGLUT2 Antibody (2952) [NBP2-46641] - Staining of rat thalamus shows strong immunoreactivity in glutamatergic synapses.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-NBP2-46641-img0009.jpg)
![Immunohistochemistry: VGLUT2 Antibody (CL2952) [NBP2-46641] - VGLUT2 Antibody (2952) [NBP2-46641] - Staining of mouse olfactory bulb shows strong immunoreactivity in glomeruli.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-NBP2-46641-img0010.jpg)
![Immunohistochemistry-Paraffin: VGLUT2 Antibody (CL2952) [NBP2-46641] - Staining of human cerebellum shows strong immunoreactivity in glutamatergic synapses in the molecular and granular layers.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-Paraffin-NBP2-46641-img0011.jpg)
![Immunohistochemistry: VGLUT2 Antibody (CL2952) [NBP2-46641] - VGLUT2 Antibody (2952) [NBP2-46641] - Staining of rat cerebellum shows strong immunoreactivity in glutamatergic fibers in the molecular and granular layers.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-NBP2-46641-img0012.jpg)
![Immunohistochemistry: VGLUT2 Antibody (CL2952) [NBP2-46641] - VGLUT2 Antibody (2952) [NBP2-46641] - Staining of mouse cerebral cortex shows moderate positivity in neuropil.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-NBP2-46641-img0013.jpg)
![Immunohistochemistry-Paraffin: VGLUT2 Antibody (CL2952) [NBP2-46641] - Staining of human cerebral cortex shows moderate immunoreactivity in neuropil.](http://images.novusbio.com/fullsize/VGLUT2-Antibody-CL2952-Immunohistochemistry-Paraffin-NBP2-46641-img0014.jpg)
![Western Blot: L1CAM Antibody (OTI2A6) [NBP2-02149] - Analysis of extracts (35ug) from 9 different cell lines by using anti-L1CAM monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Western-Blot-NBP2-02149-img0012.jpg "Western Blot: L1CAM Antibody (OTI2A6) [NBP2-02149] - Analysis of extracts (35ug) from 9 different cell lines by using anti-L1CAM monoclonal antibody.")
![Immunocytochemistry/Immunofluorescence: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY L1CAM.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunocytochemistry-Immunofluorescence-NBP2-02149-img0015.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded pancreas tissue using anti-L1CAMmouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0010.jpg)
![Flow Cytometry: L1CAM Antibody (OTI2A6) [NBP2-02149] - Analysis of Jurkat cells, using anti-L1CAM antibody, (Red) compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Flow-Cytometry-NBP2-02149-img0002.jpg)
![Western Blot: L1CAM Antibody (OTI2A6) [NBP2-02149] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY L1CAM (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-L1CAM.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Western-Blot-NBP2-02149-img0003.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded endometrium tissue within the normal limits using anti-L1CAM mouse monoclonal antibody. Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0017.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded Adenocarcinoma of colon tissue using anti-L1CAMmouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0004.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded Adenocarcinoma of ovary tissue using anti-L1CAM mouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0005.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded breast tissue using anti-L1CAM mouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0006.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded colon tissue using anti-L1CAM mouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0007.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded Kidney tissue using anti-L1CAM mouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0008.jpg)
![Immunohistochemistry-Paraffin: L1CAM Antibody (OTI2A6) [NBP2-02149] - Staining of paraffin-embedded Ovary tissue using anti-L1CAM mouse monoclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunohistochemistry-Paraffin-NBP2-02149-img0009.jpg)
![Flow Cytometry: L1CAM Antibody (OTI2A6) [NBP2-02149] - Analysis of Hela cells, using anti-L1CAM antibody, (Red) compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Flow-Cytometry-NBP2-02149-img0001.jpg)
![Immunoprecipitation: L1CAM Antibody (OTI2A6) [NBP2-02149] - Immunoprecipitation of L1CAM by using TrueMab monoclonal anti-L1CAM antibody (Negative control: IP without adding anti-L1CAM antibody). For each experiment, 500ul of DDK tagged L1CAM overexpression lysates (at 1:5 dilution with HEK293T lysate), 2ug of anti-L1CAM antibody and 20ul (0.1mg) of goat anti-mouse conjugated magnetic beads were mixed and incubated overnight. After extensive wash to remove any non-specific binding, the immuno-precipitated products were analyzed with rabbit anti-DDK polyclonal antibody.](http://images.novusbio.com/fullsize/L1CAM-Antibody-OTI2A6-Immunoprecipitation-NBP2-02149-img0018.jpg)
![Western Blot: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Analysis of extracts (35ug) from 9 different cell lines by using anti-Neurogenin 1 monoclonal antibody.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Western-Blot-NBP1-47871-img0020.jpg "Western Blot: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Analysis of extracts (35ug) from 9 different cell lines by using anti-Neurogenin 1 monoclonal antibody.")
![Immunocytochemistry/Immunofluorescence: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - COS7 cells transiently transfected by pCMV6-ENTRY Neurogenin-1.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunocytochemistry-Immunofluorescence-NBP1-47871-img0011.jpg)
![Immunohistochemistry-Paraffin: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Staining of Human prostate tissue.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunohistochemistry-Paraffin-NBP1-47871-img0017.jpg)
![Western Blot: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Neurogenin 1 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-Neurogenin 1.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Western-Blot-NBP1-47871-img0019.jpg)
![Immunohistochemistry-Paraffin: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Staining of Human colon tissue.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunohistochemistry-Paraffin-NBP1-47871-img0012.jpg)
![Immunohistochemistry-Paraffin: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Staining of Human Kidney tissue.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunohistochemistry-Paraffin-NBP1-47871-img0013.jpg)
![Immunohistochemistry-Paraffin: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Staining of Human lung tissue.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunohistochemistry-Paraffin-NBP1-47871-img0014.jpg)
![Immunohistochemistry-Paraffin: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Staining of Human Ovary tissue.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunohistochemistry-Paraffin-NBP1-47871-img0015.jpg)
![Immunohistochemistry-Paraffin: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Staining of Human pancreas tissue.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunohistochemistry-Paraffin-NBP1-47871-img0016.jpg)
![Immunoprecipitation: Neurogenin-1 Antibody (OTI3F9) [NBP1-47871] - Immunoprecipitation (IP) of NEUROG1 by using TrueMab monoclonal anti-NEUROG1 antibodies (Negative control: IP without adding anti-NEUROG1 antibody.). For each experiment, 500ul of DDK tagged NEUROG1 overexpression lysates (at 1:5 dilution with HEK293T lysate), 2ug of anti-NEUROG1 antibody and 20ul (0.1mg) of goat anti-mouse conjugated magnetic beads were mixed and incubated overnight. After extensive wash to remove any non-specific binding, the immuno-precipitated products were analyzed with rabbit anti-DDK polyclonal antibody.](http://images.novusbio.com/fullsize/Neurogenin-1-Antibody-OTI3F9-Immunoprecipitation-NBP1-47871-img0021.jpg)
![Western Blot: Tyrosine Hydroxylase [p Ser31] Antibody [NB300-211] - PC-12 cells incubated in the absence (Control) and presence of okadaic acid (OA, 1 uM for 60 min) showing specific immunolabeling of the ~60 kDa TH phosphorylated at Ser31.](http://images.novusbio.com/fullsize/Tyrosine-Hydroxylase-[p-Ser31]-Antibody-Western-Blot-NB300-211-img0001.jpg "Western Blot: Tyrosine Hydroxylase [p Ser31] Antibody [NB300-211] - PC-12 cells incubated in the absence (Control) and presence of okadaic acid (OA, 1 uM for 60 min) showing specific immunolabeling of the ~60 kDa TH phosphorylated at Ser31.")
![Western Blot: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - Lane 1: Molecular Weight Ladder (MW). Lane 2: Active Alpha Synuclein Protein Aggregate.](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-Western-Blot-NBP2-54789-img0005.jpg "Western Blot: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - Lane 1: Molecular Weight Ladder (MW). Lane 2: Active Alpha Synuclein Protein Aggregate.")
![Immunocytochemistry/Immunofluorescence: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - Primary rat hippocampal neurons show lewy body inclusion formation when treated with active Alpha Synuclein Protein Aggregate at 4 ug/ml (D-F), but not when treated with control Alpha Synuclein Protein Aggregate at 4 ug/ml (A-C). Tissue: Primary hippocampal neurons. Species: Sprague-Dawley rat. Fixation: 4% formaldehyde from PFA. Primary Antibody: Mouse anti-pSer129 Antibody at 1:1000 24 hours at 4C. Secondary Antibody: FITC Goat Anti-Mouse (green) at 1:700 for 1 hours at RT. Counterstain: Hoechst (blue) nuclear stain at 1:4000 for 1 hour at RT. Localization: Lewy body incluscions. Magnification: 20x.](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-Immunocytochemistry-Immunofluorescence-NBP2-54789-img0004.jpg)
![Immunohistochemistry: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - Immunohistochemistry analysis of rat brain injected with Type 1 human alpha synuclein PFFs (NBP2-54789). Species: Female Sprague-Dawley Rat. Rat was injected with 16g Type 1 human alpha synuclein PFFs (NBP2-54789) in each of 2 injection sites: AP+1.6, ML+2.4, DV-4.2 from skull; and AP-1.4, ML+0.2, DV-2.8 from skull. 30-days post-injection. Fixation: Saline perfusion followed by 4% PFA fixation for 48 hrs. Primary antibody: rabbit monoclonal anti-pSer129 alpha synuclein. Secondary Antibody: Biotin-SP Donkey Anti-Rabbit IgG (H+L) at 1:500 for 2 hours in cold room with shaking. ABC signal amplification, DAB staining. Magnification: 20X. Alpha synuclein pathology is seen in the striatum close to an injection site.](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-Immunohistochemistry-NBP2-54789-img0007.jpg)
![In vitro assay: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - Thioflavin T emission curves show increased fluorescence (correlated to alpha Synuclein protein aggregation) over time when 10 nM of active alpha Synuclein aggregate (NBP2-54789) is combined with 100 uM of active alpha Synuclein monomer (NBP2-54788), as compared to active alpha Synuclein aggregate (NBP2-54789) and active alpha Synuclein monomer (NBP2-54788) alone. Thioflavin T ex = 450 nm, em = 485 nm.](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-In-vitro-assay-NBP2-54789-img0006.jpg)
![Electron Microscopy: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - TEM of Type 1 alpha-Synuclein Pre-formed Fibrils (PFFs) (NBP2-54789)](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-Electron-Microscopy-NBP2-54789-img0008.jpg)
![Product Image: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - Toxicity results comparing Active Human Recombinant alpha-Synuclein Pre-formed Fibrils (Type 2) and Active Human Recombinant alpha-Synuclein Pre-formed Fibrils (Type 1) (Catalog No. NBP2-54789). Data was graphed after live cell imaging results were obtained using the following procedure: After 8 days in vitro, primary rat mixed cortical neuron cells were washed with 1X PBS and treated with 500 g/ml of Type 1 and Type 2 alpha-Synuclein Proteins for 20 hours at 37C. Following treatements, cells were washed with 2X PBS and incubated with a staining solution (2.0 M Cell Event + 2.5 M Ethidium homodimer + 2.5 g/ml Hoechst 33342 in sterile HBSS) for 30 minutes at 37C. The addition of the Type 2 alpha-Synuclein Proteins resulted in a significant increase in cell death.](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-Product-Image-NBP2-54789-img0010.jpg)
![Electron Microscopy: Recombinant Human alpha-Synuclein Active, Pre-formed Fibrils, (Type 1) Protein [NBP2-54789] - TEM of Type 1 alpha-Synuclein Pre-formed Fibrils (PFFs) (NBP2-54789)](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Pre-formed-Fibrils-Type-1-Protein-Electron-Microscopy-NBP2-54789-img0009.jpg)
![Western Blot: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of TrkA on rat brain tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA 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/TrkA-Antibody-JJ084-04-Western-Blot-NBP2-67473-img0010.jpg "Western Blot: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of TrkA on rat brain tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA 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.")
![Immunocytochemistry/Immunofluorescence: TrkA Antibody (JJ084-04) [NBP2-67473] - Staining TrkA in N2A cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Immunocytochemistry-Immunofluorescence-NBP2-67473-img0008.jpg)
![Immunohistochemistry-Paraffin: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of paraffin-embedded mouse liver tissue using anti-TrkA antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Immunohistochemistry-Paraffin-NBP2-67473-img0006.jpg)
![Flow Cytometry: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of SH-SY-5Y cells with TrkA antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Flow-Cytometry-NBP2-67473-img0001.jpg)
![Western Blot: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of TrkA on different lysates using anti-TrkA antibody at 1/1,000 dilution. Positive control: Lane 1: Mouse brain Lane 2: SH-SY-5Y](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Western-Blot-NBP2-67473-img0007.jpg)
![Western Blot: TrkA Antibody (JJ084-04) [NBP2-67473] - Western blot analysis of TrkA on N2A cell lysates using anti-TrkA antibody at 1/500 dilution.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Western-Blot-NBP2-67473-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: TrkA Antibody (JJ084-04) [NBP2-67473] - Staining TrkA in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Immunocytochemistry-Immunofluorescence-NBP2-67473-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: TrkA Antibody (JJ084-04) [NBP2-67473] - Staining TrkA in SH-SY-5Y cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Immunocytochemistry-Immunofluorescence-NBP2-67473-img0003.jpg)
![Immunohistochemistry-Paraffin: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of paraffin-embedded human tonsil tissue using anti-TrkA antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Immunohistochemistry-Paraffin-NBP2-67473-img0004.jpg)
![Immunohistochemistry-Paraffin: TrkA Antibody (JJ084-04) [NBP2-67473] - Analysis of paraffin-embedded mouse kidney tissue using anti-TrkA antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/TrkA-Antibody-JJ084-04-Immunohistochemistry-Paraffin-NBP2-67473-img0005.jpg)