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![Immunocytochemistry/Immunofluorescence: Neuropeptide Y Antibody [NBP2-38804] - Staining of human cell line SH-SY5Y shows localization to the Golgi apparatus. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/Neuropeptide-Y-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-38804-img0003.jpg "Immunocytochemistry/Immunofluorescence: Neuropeptide Y Antibody [NBP2-38804] - Staining of human cell line SH-SY5Y shows localization to the Golgi apparatus. Antibody staining is shown in green.")
![Immunohistochemistry-Paraffin: Neuropeptide Y Antibody [NBP2-38804] - Staining of human cerebral cortex shows moderate cytoplasmic positivity in neuronal cells. Distinct staining was observed in fraction of neuropil.](http://images.novusbio.com/fullsize/Neuropeptide-Y-Antibody-Immunohistochemistry-NBP2-38804-img0002.jpg)
![ELISA: Human Beta-endorphin ELISA Kit (Colorimetric) [NBP2-78774] - Samples were spiked with high concentrations of Human Beta-endorphin and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp2-78774_human-beta-endorphin-elisa-kit-colorimetric-132202416201992.jpg "ELISA: Human Beta-endorphin ELISA Kit (Colorimetric) [NBP2-78774] - Samples were spiked with high concentrations of Human Beta-endorphin and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.")
![ELISA: Human Beta-endorphin ELISA Kit (Colorimetric) [NBP2-78774] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-78774_human-beta-endorphin-elisa-kit-colorimetric-4320249133269.jpg)
![ELISA: Mouse ACTH ELISA Kit (Colorimetric) [NBP3-14759] - Samples were spiked with high concentrations of Mouse ACTH and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp3-14759_mouse-acth-elisa-kit-colorimetric-13220241685392.jpg "ELISA: Mouse ACTH ELISA Kit (Colorimetric) [NBP3-14759] - Samples were spiked with high concentrations of Mouse ACTH and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.")
![ELISA: Mouse ACTH ELISA Kit (Colorimetric) [NBP3-14759] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-14759_mouse-acth-elisa-kit-colorimetric-432024941585.jpg)
![Western Blot: VIP Antibody [NBP3-12900] - VIP antibody detects VIP protein by western blot analysis. Whole cell extracts (30 ug) was separated by 15% SDS-PAGE, and the membrane was blotted with VIP antibody (NBP3-12900) at a dilution of 1:1000.](http://images.novusbio.com/fullsize/VIP-Antibody-Western-Blot-NBP3-12900-img0001.jpg "Western Blot: VIP Antibody [NBP3-12900] - VIP antibody detects VIP protein by western blot analysis. Whole cell extracts (30 ug) was separated by 15% SDS-PAGE, and the membrane was blotted with VIP antibody (NBP3-12900) at a dilution of 1:1000.")
![Immunohistochemistry-Frozen: VIP Antibody [NBP3-12900] - VIP antibody detects VIP protein by immunohistochemical analysis. Sample: Frozen-sectioned mouse cerebral cortex. Green: VIP stained by VIP antibody (NBP3-12900) diluted at 1:250. Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/VIP-Antibody-Immunohistochemistry-Frozen-NBP3-12900-img0002.jpg)
![Western Blot: GNAT3 Antibody [NBP3-05122] - Analysis of extracts of A-549 cells, using GNAT3 antibody 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 .](http://images.novusbio.com/fullsize/GNAT3-Antibody-Western-Blot-NBP3-05122-img0001.jpg "Western Blot: GNAT3 Antibody [NBP3-05122] - Analysis of extracts of A-549 cells, using GNAT3 antibody 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 .")
![Immunocytochemistry/ Immunofluorescence: GNAT3 Antibody - Azide and BSA Free [NBP3-05122] - Immunofluorescence analysis of NIH/3T3 cells using GNAT3 Rabbit pAb (A15982) at dilution of 1:100. Secondary antibody: Cy3 Goat Anti-Rabbit IgG (H+L) (AS007) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-05122_rabbit-polyclonal-gnat3-antibody-52202519294510.jpg)
![Immunohistochemistry-Paraffin: CRHR1/CRF1 Antibody [NLS1779] - Analysis of anti-CRF1 antibody with rat hypothalalmus at 21 ug/ml.](http://images.novusbio.com/fullsize/CRHR1-CRF1-Antibody-Immunohistochemistry-Paraffin-NLS1779-img0004.jpg "Immunohistochemistry-Paraffin: CRHR1/CRF1 Antibody [NLS1779] - Analysis of anti-CRF1 antibody with rat hypothalalmus at 21 ug/ml.")
![Immunohistochemistry-Paraffin: CRHR1/CRF1 Antibody [NLS1779] - Analysis of anti-CRF1 antibody with human brain, neurons and glia at 21 ug/ml.](http://images.novusbio.com/fullsize/CRHR1-CRF1-Antibody-Immunohistochemistry-Paraffin-NLS1779-img0003.jpg)
![Immunohistochemistry: Galanin Antibody (4B3) [NBP3-09010] - Formalin fixed rat prostate slices were were stained with NBP3-09010 at 3 ug/ml.](http://images.novusbio.com/fullsize/Galanin-Antibody-4B3-Immunohistochemistry-NBP3-09010-img0001.jpg "Immunohistochemistry: Galanin Antibody (4B3) [NBP3-09010] - Formalin fixed rat prostate slices were were stained with NBP3-09010 at 3 ug/ml.")
![Western Blot: CACNA1S Antibody [NBP1-31659] - Sample (30 ug of whole cell lysate) A: 293T 5% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/CACNA1S-Antibody-Western-Blot-NBP1-31659-img0004.jpg "Western Blot: CACNA1S Antibody [NBP1-31659] - Sample (30 ug of whole cell lysate) A: 293T 5% SDS PAGE; antibody diluted at 1:1000.")
![Immunohistochemistry-Paraffin: CACNA1S Antibody [NBP1-31659] - Paraffin-embedded Cal27 xenograft, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/CACNA1S-Antibody-Immunohistochemistry-Paraffin-NBP1-31659-img0003.jpg)
![Western Blot: MCT8/SLC16A2 Antibody [NBP2-32109] - Whole cell lysate (50 ug) from HeLa, 293T, Jurkat, and mouse TCMK-1 cells. Antibodies: Affinity purified rabbit anti-MCT8 antibody NBP2-32109 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/MCT8-SLC16A2-Antibody-Western-Blot-NBP2-32109-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: MCT8/SLC16A2 Antibody [NBP2-32109] - Whole cell lysate (50 ug) from HeLa, 293T, Jurkat, and mouse TCMK-1 cells. Antibodies: Affinity purified rabbit anti-MCT8 antibody NBP2-32109 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")
![<b>Independent Antibodies Validation and Biological Strategies Validation.</b>Immunoprecipitation: MCT8/SLC16A2 Antibody [NBP2-32109] - Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from 293T and cells. Antibodies: Affinity purified rabbit anti-MCT8 antibodyNBP2-32109 used for IP at 6 ug per reaction. MCT8 was also immunoprecipitated by rabbit anti-MCT8 antibody BL16310. For blotting immunoprecipitated MCT8,NBP2-32109 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/MCT8-SLC16A2-Antibody-Western-Blot-NBP2-32109-img0002.jpg)
![Western Blot: PER1 Antibody [NBP3-12882] - Untreated (-) and treated (+) HeLa whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER1 antibody (NBP3-12882) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/PER1-Antibody-Western-Blot-NBP3-12882-img0003.jpg "Western Blot: PER1 Antibody [NBP3-12882] - Untreated (-) and treated (+) HeLa whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER1 antibody (NBP3-12882) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![Western Blot: PER1 Antibody [NBP3-12882] - Whole cell extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with PER1 antibody (NBP3-12882) 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/PER1-Antibody-Western-Blot-NBP3-12882-img0001.jpg)
![Western Blot: PER1 Antibody [NBP3-12882] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER1 antibody (NBP3-12882) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/PER1-Antibody-Western-Blot-NBP3-12882-img0002.jpg)