| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-88622-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-17286-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-87532-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB120-3439-25ug | |||
![Western Blot: VIP Antibody [NBP3-12899] - 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 (NBP3-12899) diluted at 1:1000.](http://images.novusbio.com/fullsize/VIP-Antibody-Western-Blot-NBP3-12899-img0001.jpg "Western Blot: VIP Antibody [NBP3-12899] - 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 (NBP3-12899) diluted at 1:1000.")
![Immunocytochemistry/Immunofluorescence: VIP Antibody [NBP3-12899] - VIP antibody detects VIP protein by immunofluorescent analysis. Sample: DIV10 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: VIP stained by VIP antibody (NBP3-12899) diluted at 1:500. Red: beta Tubulin 3/ Tuj1, stained by beta Tubulin 3/ Tuj1 antibody [GT11710] (NBP2-43559) diluted at 1:500. Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/VIP-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-12899-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: NPAS3 Antibody [NBP1-88622] - Staining of human cell line U-251 MG shows localization to nucleoplasm.](http://images.novusbio.com/fullsize/NPAS3-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-88622-img0017.jpg "Immunocytochemistry/Immunofluorescence: NPAS3 Antibody [NBP1-88622] - Staining of human cell line U-251 MG shows localization to nucleoplasm.")
![Immunohistochemistry-Paraffin: NPAS3 Antibody [NBP1-88622] -Staining of human cerebral cortex shows strong nuclear positivity in neurons.](http://images.novusbio.com/fullsize/antibody/nbp1-88622_rabbit-polyclonal-npas3-antibody-immunohistochemistry-paraffin-22820248269..jpg)
![Immunocytochemistry/Immunofluorescence: NPAS3 Antibody [NBP3-17286] - Staining of human cell line AF22 shows localization to nucleoplasm.](http://images.novusbio.com/fullsize/NPAS3-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-17286-img0002.jpg "Immunocytochemistry/Immunofluorescence: NPAS3 Antibody [NBP3-17286] - Staining of human cell line AF22 shows localization to nucleoplasm.")
![Immunohistochemistry-Paraffin: NPAS3 Antibody [NBP3-17286] - Staining of human small intestine shows strong nuclear positivity in glandular cells.](http://images.novusbio.com/fullsize/NPAS3-Antibody-Immunohistochemistry-Paraffin-NBP3-17286-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: Synaptogyrin 1 Antibody [NBP1-87532] - Staining of human cell line A-431 shows localization to cytosol.](http://images.novusbio.com/fullsize/Synaptogyrin-1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-87532-img0004.jpg "Immunocytochemistry/Immunofluorescence: Synaptogyrin 1 Antibody [NBP1-87532] - Staining of human cell line A-431 shows localization to cytosol.")
![Immunohistochemistry-Paraffin: Synaptogyrin 1 Antibody [NBP1-87532] - Staining of human cerebellum shows distinct positivity in neuropil.](http://images.novusbio.com/fullsize/Synaptogyrin-1-Antibody-Immunohistochemistry-NBP1-87532-img0003.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)
![Immunohistochemistry-Paraffin: GPR50 Antibody [NLS751] - Analysis of anti-GPR50 antibody with human brain, glioblastoma.](http://images.novusbio.com/fullsize/GPR50-Antibody-Immunohistochemistry-Paraffin-NLS751-img0003.jpg "Immunohistochemistry-Paraffin: GPR50 Antibody [NLS751] - Analysis of anti-GPR50 antibody with human brain, glioblastoma.")
![Immunohistochemistry-Paraffin: GPR50 Antibody [NLS751] - Analysis of anti-GPR50 antibody with human brain, hypothalamus at 10 ug/ml.](http://images.novusbio.com/fullsize/GPR50-Antibody-Immunohistochemistry-Paraffin-NLS751-img0002.jpg)
![Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER2 antibody [HL2775] (NBP3-48535) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-48535_rabbit-per2-mab-hl2775-western-blot-1411202518392018.jpg "<b>Genetic Strategies Validation. </b>Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER2 antibody [HL2775] (NBP3-48535) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![<b>Genetic Strategies Validation. </b>Treated 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER2 antibody [HL2775] (NBP3-48535) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-48535_rabbit-per2-mab-hl2775-western-blot-1411202518365911.jpg)
![Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with PER2 antibody [HL2775] (NBP3-48535) diluted at 1:100000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48535_rabbit-per2-mab-hl2775-western-blot-1411202518404322.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)
![Dopamine Receptor D4 antibody [HL2850] (NBP3-48738) detects Dopamine Receptor D4 protein by flow cytometry analysis. Sample: Non-transfected and transfected 293T cells were fixed in 4% paraformaldehyde at 4C for 15 min and washed with 0.1% saponin buffer. The cells were following stained with Dopamine Receptor D4 antibody [HL2850] (NBP3-48738) diluted at 1:50 or a Rabbit monoclonal IgG isotype control at 4C for 1 hour.](http://images.novusbio.com/fullsize/nbp3-48738_rabbit-dopamine-receptor-d4-mab-hl2850-flow-cytometry-141120251840163.jpg "Dopamine Receptor D4 antibody [HL2850] (NBP3-48738) detects Dopamine Receptor D4 protein by flow cytometry analysis. Sample: Non-transfected and transfected 293T cells were fixed in 4% paraformaldehyde at 4C for 15 min and washed with 0.1% saponin buffer. The cells were following stained with Dopamine Receptor D4 antibody [HL2850] (NBP3-48738) diluted at 1:50 or a Rabbit monoclonal IgG isotype control at 4C for 1 hour.")
![Dopamine Receptor D4 antibody [HL2850] detects Dopamine Receptor D4 protein at cell membrane by immunohistochemical analysis.Sample: Paraffin-embedded human stomach tumor.Dopamine Receptor D4 stained by Dopamine Receptor D4 antibody [HL2850] (NBP3-48738) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-48738_rabbit-dopamine-receptor-d4-mab-hl2850-immunohistochemistry-paraffin-1411202518243313.jpg)
![<b>Orthogonal Strategies Validation. </b>Unboiled Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Dopamine Receptor D4 antibody [HL2850] (NBP3-48738) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48738_rabbit-dopamine-receptor-d4-mab-hl2850-western-blot-1411202518395422.jpg)
![Western Blot: Serotonin N-acetyltransferase [p Thr29] Antibody [NB120-3439] - Analysis of phospho AA-NAT in transfected 293T cell lysate.](http://images.novusbio.com/fullsize/Serotonin-N-acetyltransferase-[p-Thr29]-Antibody-Western-Blot-NB120-3439-img0003.jpg "Western Blot: Serotonin N-acetyltransferase [p Thr29] Antibody [NB120-3439] - Analysis of phospho AA-NAT in transfected 293T cell lysate.")
![Western Blot: BMAL1 Antibody [NBP1-28802] - (0.3ug/ml) staining of Human Brain (Cerebellum) 35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/BMAL1-Antibody-Western-Blot-NBP1-28802-img0001.jpg "Western Blot: BMAL1 Antibody [NBP1-28802] - (0.3ug/ml) staining of Human Brain (Cerebellum) 35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")