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![ELISA: Human Tyrosine Hydroxylase ELISA Kit (Colorimetric) [NBP3-06920] - Samples were spiked with high concentrations of Human Tyrosine Hydroxylase and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp3-06920_human-tyrosine-hydroxylase-elisa-kit-colorimetric-1322024168531.jpg "ELISA: Human Tyrosine Hydroxylase ELISA Kit (Colorimetric) [NBP3-06920] - Samples were spiked with high concentrations of Human Tyrosine Hydroxylase and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.")
![ELISA: Human Tyrosine Hydroxylase ELISA Kit (Colorimetric) [NBP3-06920] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-06920_human-tyrosine-hydroxylase-elisa-kit-colorimetric-432024857426.jpg)
![ELISA: Mouse alpha-Synuclein ELISA Kit (Colorimetric) [NBP3-08174] - Image from verified customer review.](http://images.novusbio.com/fullsize/nbp3-08174_mouse-alpha-synuclein-elisa-kit-colorimetric-elisa-1962023111722..jpg "ELISA: Mouse alpha-Synuclein ELISA Kit (Colorimetric) [NBP3-08174] - Image from verified customer review.")
![ELISA: Mouse alpha-Synuclein ELISA Kit (Colorimetric) [NBP3-08174] - DRC. Image from verified customer review.](http://images.novusbio.com/fullsize/nbp3-08174_mouse-alpha-synuclein-elisa-kit-colorimetric-258202314226.png)
![ELISA: Mouse alpha-Synuclein ELISA Kit (Colorimetric) [NBP3-08174] - Samples were spiked with high concentrations of Mouse alpha-Synuclein and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp3-08174_mouse-alpha-synuclein-elisa-kit-colorimetric-132202416225238.jpg)
![ELISA: Mouse alpha-Synuclein ELISA Kit (Colorimetric) [NBP3-08174] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-08174_mouse-alpha-synuclein-elisa-kit-colorimetric-4320249141641.jpg)
![Western Blot: Ankyrin 3 Antibody [NBP2-58275] - Analysis in human cell line SK-BR-3.](http://images.novusbio.com/fullsize/Ankyrin-3-Antibody-Western-Blot-NBP2-58275-img0002.jpg "Western Blot: Ankyrin 3 Antibody [NBP2-58275] - Analysis in human cell line SK-BR-3.")
![Immunocytochemistry/Immunofluorescence: Ankyrin 3 Antibody [NBP2-58275] - Staining of human cell line U-2 OS shows localization to plasma membrane.](http://images.novusbio.com/fullsize/Ankyrin-3-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-58275-img0001.jpg)
![Western Blot: HSP27 [p Ser82] Antibody [NBP3-13297] - Untreated (-) and treated (+) C2C12 whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 (phospho Ser82) antibody (NBP3-13297) 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/HSP27-[p-Ser82]-Antibody-Western-Blot-NBP3-13297-img0003.jpg "<b>Biological Strategies Validation. </b>Western Blot: HSP27 [p Ser82] Antibody [NBP3-13297] - Untreated (-) and treated (+) C2C12 whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 (phospho Ser82) antibody (NBP3-13297) 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.")
![<b>Biological Strategies Validation. </b>Western Blot: HSP27 [p Ser82] Antibody [NBP3-13297] - Untreated (-) and treated (+) HeLa whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 (phospho Ser82) antibody (NBP3-13297) 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/HSP27-[p-Ser82]-Antibody-Western-Blot-NBP3-13297-img0001.jpg)
![Western Blot: HSP27 [p Ser82] Antibody [NBP3-13297] - Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 (phospho Ser82) antibody (NBP3-13297) 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/HSP27-[p-Ser82]-Antibody-Western-Blot-NBP3-13297-img0002.jpg)
![Western Blot: Nicotinic Acetylcholine R alpha 4/CHRNA4 Antibody [NBP1-00143] - Analysis of Nicotinic Acetylcholine Receptor alpha 4 in Rat Brain lysate (35ug protein in RIPA buffer) using this antibody at 0.3ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Nicotinic-Acetylcholine-R-alpha-4-CHRNA4-Antibody-Western-Blot-NBP1-00143-img0003.jpg "Western Blot: Nicotinic Acetylcholine R alpha 4/CHRNA4 Antibody [NBP1-00143] - Analysis of Nicotinic Acetylcholine Receptor alpha 4 in Rat Brain lysate (35ug protein in RIPA buffer) using this antibody at 0.3ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.")
![Western Blot: Doublecortin Antibody [NBP2-26149] - NBP2-26149 (0.5ug/ml) staining of Mouse fetal Brain lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Doublecortin-Antibody-Western-Blot-NBP2-26149-img0001.jpg "Western Blot: Doublecortin Antibody [NBP2-26149] - NBP2-26149 (0.5ug/ml) staining of Mouse fetal Brain lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")
![Immunocytochemistry/Immunofluorescence: Doublecortin Antibody [NBP2-26149] - Analysis of paraformaldehyde fixed HepG2 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (5ug/ml) followed by Alexa Fluor 488 secondary antibody (1ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (1ug/ml)](http://images.novusbio.com/fullsize/Doublecortin-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-26149-img0003.jpg)
![Immunohistochemistry-Paraffin: TRPM7 Antibody [NB100-810] - (4ug/ml) staining of paraffin embedded Mouse Hippocampus. Steamed antigen retrieval with citrate buffer pH 6, HRP-staining. Similar results were obtained after antigen retrieval at pH9.](http://images.novusbio.com/fullsize/TRPM7-Antibody-Immunohistochemistry-Paraffin-NB100-810-img0004.jpg "Immunohistochemistry-Paraffin: TRPM7 Antibody [NB100-810] - (4ug/ml) staining of paraffin embedded Mouse Hippocampus. Steamed antigen retrieval with citrate buffer pH 6, HRP-staining. Similar results were obtained after antigen retrieval at pH9.")
![Western Blot: iNOS Antibody (3L0U6) [NBP3-16273] - Western blot analysis of lysates from RAW 264.7 cells using iNOS Rabbit mAb at 1:1000 dilution incubated overnight at 4C. Raw264.7 cells were treated by LPS (1 ug/ml) at 37C for 8 hours.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 30 ug per lane. Blocking buffer: 3 % nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s.](http://images.novusbio.com/fullsize/nbp3-16273_rabbit-inos-mab-3l0u6-5220251265374.jpg "Western Blot: iNOS Antibody (3L0U6) [NBP3-16273] - Western blot analysis of lysates from RAW 264.7 cells using iNOS Rabbit mAb at 1:1000 dilution incubated overnight at 4C. Raw264.7 cells were treated by LPS (1 ug/ml) at 37C for 8 hours.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 30 ug per lane. Blocking buffer: 3 % nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s.")
![Immunocytochemistry/ Immunofluorescence: iNOS Antibody (3L0U6) [NBP3-16273] - Confocal imaging of RAW 264.7 cells (treated with LPS) and RAW 264.7 cells(untreated) using iNOS Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . DAPI was used for nuclear staining (Blue). Objective: 100x.](http://images.novusbio.com/fullsize/nbp3-16273_rabbit-inos-mab-3l0u6-52202511392210.jpg)