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![ELISA: Human Fatty Acid Synthase/FASN ELISA Kit (Colorimetric) [NBP2-82512] - Samples were spiked with high concentrations of Human Fatty Acid Synthase/FASN and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp2-82512_human-fatty-acid-synthase-fasn-elisa-kit-colorimetric-13220241692297.jpg "ELISA: Human Fatty Acid Synthase/FASN ELISA Kit (Colorimetric) [NBP2-82512] - Samples were spiked with high concentrations of Human Fatty Acid Synthase/FASN and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.")
![ELISA: Human Fatty Acid Synthase/FASN ELISA Kit (Colorimetric) [NBP2-82512] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-82512_human-fatty-acid-synthase-fasn-elisa-kit-colorimetric-4320249141626.jpg)
![Western Blot: CLOCK Antibody (3D8H6) [NBP3-16656] - Western blot analysis of extracts of various cell lines, using CLOCK Rabbit mAb (NBP3-16656) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 3s.](http://images.novusbio.com/fullsize/CLOCK-Antibody-3D8H6-Western-Blot-NBP3-16656-img0004.jpg "Western Blot: CLOCK Antibody (3D8H6) [NBP3-16656] - Western blot analysis of extracts of various cell lines, using CLOCK Rabbit mAb (NBP3-16656) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 3s.")
![Immunocytochemistry/Immunofluorescence: Fatty Acid Synthase/FASN Antibody (2A5) [NBP3-26589] - Staining of Hela Cells with Fatty Acid Synthase/FASN Antibody (2A5) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26589_rabbit-fatty-acid-synthase-fasn-mab-2a5-282202412493622.jpg "Immunocytochemistry/Immunofluorescence: Fatty Acid Synthase/FASN Antibody (2A5) [NBP3-26589] - Staining of Hela Cells with Fatty Acid Synthase/FASN Antibody (2A5) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: Fatty Acid Synthase/FASN Antibody (2A5) [NBP3-26589] - Overlay histogram showing A549 cells stained with Fatty Acid Synthase/FASN Antibody (2A5) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min 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/nbp3-26589_rabbit-fatty-acid-synthase-fasn-mab-2a5-282202414183634.jpg)
![SDS-Page: Recombinant Human COX4 Protein [H00001327-Q01] - 12.5% SDS-PAGE Stained with Coomassie Blue.](http://images.novusbio.com/fullsize/qc_test-H00001327-Q01-1.jpg "SDS-Page: Recombinant Human COX4 Protein [H00001327-Q01] - 12.5% SDS-PAGE Stained with Coomassie Blue.")
![ELISA: Human NMDAR2A ELISA Kit (Colorimetric) [NBP2-82196] - Samples were spiked with high concentrations of Human NMDAR2A and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp2-82196_human-nmdar2a-elisa-kit-colorimetric-132202416143099.jpg "ELISA: Human NMDAR2A ELISA Kit (Colorimetric) [NBP2-82196] - Samples were spiked with high concentrations of Human NMDAR2A and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.")
![ELISA: Human NMDAR2A ELISA Kit (Colorimetric) [NBP2-82196] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-82196_human-nmdar2a-elisa-kit-colorimetric-432024941578.jpg)
![Western Blot: TrkB Antibody (1D7U4) [NBP3-15948] - Western blot analysis of extracts of various cell lines, using TrkB antibody (NBP3-15948) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 180s.](http://images.novusbio.com/fullsize/TrkB-Antibody-1D7U4-Western-Blot-NBP3-15948-img0001.jpg "Western Blot: TrkB Antibody (1D7U4) [NBP3-15948] - Western blot analysis of extracts of various cell lines, using TrkB antibody (NBP3-15948) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 180s.")
![Western Blot: NMDAR2A Antibody [NBP3-10351] - WB Suggested Anti-NMDAR2A Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: Human Muscle](http://images.novusbio.com/fullsize/NMDAR2A Antibody-Western Blot-NBP3-10351-img0001.jpg "Western Blot: NMDAR2A Antibody [NBP3-10351] - WB Suggested Anti-NMDAR2A Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: Human Muscle")
![Western Blot: TrkB Antibody (SR2271) [NBP3-22076] - Western blot analysis using NBP3-22076 in mouse brain lysate.](http://images.novusbio.com/fullsize/nbp3-22076_rabbit-trkb-mab-sr2271-5720231531213.jpg "Western Blot: TrkB Antibody (SR2271) [NBP3-22076] - Western blot analysis using NBP3-22076 in mouse brain lysate.")
![Immunohistochemistry: Substance P Antibody (JE59-73) [NBP3-32984] - Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue with Rabbit anti-Substance P antibody (NBP3-32984) at 1/200 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 (NBP3-32984) at 1/200 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/nbp3-32984_rabbit-substance-p-mab-je59-73-298202414115438.jpg "Immunohistochemistry: Substance P Antibody (JE59-73) [NBP3-32984] - Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue with Rabbit anti-Substance P antibody (NBP3-32984) at 1/200 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 (NBP3-32984) at 1/200 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.")