| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB300-605SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-22119SS | |||
| Azide and BSA Free | NBP2-80814 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-70342 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-72582 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-72584 | |||
![Western Blot: iNOS Antibody [NB300-605] - Analysis of iNOS was performed by loading 20 ug of RAW264 whole cell lysate untreated (left lane) or stimulated with LPS at 1 ug/mL for 16 hours (right lane) and 10 uL of PageRuler Plus Prestained Protein Ladder onto a 4-20% Tris-Glycine polyacrylamide gel. Proteins were transferred to a nitrocellulose membrane and blocked with 5% Milk in TBST for at least 1 hour. The membrane was probed with an iNOS Rabbit polyclonal antibody at a dilution of 1:1000 overnight at 4C on a rocking platform, washed in TBST, and probed with a Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP conjugate at a dilution of 1:1000 for 1 hour. Chemiluminescent detection was performed using SuperSignal West Pico.](http://images.novusbio.com/fullsize/iNOS-Antibody-Western-Blot-NB300-605-img0015.jpg "<b>Biological Strategies Validation. </b>Western Blot: iNOS Antibody [NB300-605] - Analysis of iNOS was performed by loading 20 ug of RAW264 whole cell lysate untreated (left lane) or stimulated with LPS at 1 ug/mL for 16 hours (right lane) and 10 uL of PageRuler Plus Prestained Protein Ladder onto a 4-20% Tris-Glycine polyacrylamide gel. Proteins were transferred to a nitrocellulose membrane and blocked with 5% Milk in TBST for at least 1 hour. The membrane was probed with an iNOS Rabbit polyclonal antibody at a dilution of 1:1000 overnight at 4C on a rocking platform, washed in TBST, and probed with a Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP conjugate at a dilution of 1:1000 for 1 hour. Chemiluminescent detection was performed using SuperSignal West Pico.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: iNOS Antibody [NB300-605] - Immunohistochemistry was performed on normal deparaffinized human Lung tissue.](http://images.novusbio.com/fullsize/iNOS-Antibody-Immunohistochemistry-Paraffin-NB300-605-img0010.jpg)
![Immunohistochemistry-Paraffin: iNOS Antibody [NB300-605] - Immunohistochemistry was performed on normal deparaffinized human Heart tissue.](http://images.novusbio.com/fullsize/iNOS-Antibody-Immunohistochemistry-Paraffin-NB300-605-img0016.jpg)
![Immunocytochemistry/Immunofluorescence: iNOS Antibody [NB300-605] - Analysis of iNOS in A549 Cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a iNOS polyclonal antibody at a dilution of 1:20 overnight at 4C, washed with PBS and incubated with a DyLight 488 conjugated secondary antibody. iNOS staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown.](http://images.novusbio.com/fullsize/iNOS-Antibody-Immunocytochemistry-Immunofluorescence-NB300-605-img0012.jpg)
![<b>Biological Strategies Validation. </b>Western Blot: iNOS Antibody [NB300-605] - iNOS in stimulated astrocytes. Western blot image submitted by a verified customer review.](http://images.novusbio.com/fullsize/iNOS-Antibody-Western-Blot-NB300-605-img0005.jpg)
![<b>Biological Strategies Validation. </b>Western Blot: iNOS Antibody [NB300-605] - LCA-induced oxidative stress in 4T1 breast cancer cells. The 4T1 cells were treated with LCA for 48 h, then the indicated measurements were performed. The level of iNOS protein was detected by western blotting (n = 3). Image collected and cropped by CiteAb from the following publication (//www.mdpi.com/2072-6694/11/9/1255), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/iNOS-Antibody-Western-Blot-NB300-605-img0017.jpg)
![Immunocytochemistry/Immunofluorescence: iNOS Antibody [NB300-605] - Analysis of iNOS in NIH-3T3 Cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a iNOS polyclonal antibody at a dilution of 1:20 overnight at 4C, washed with PBS and incubated with a DyLight 488 conjugated secondary antibody. iNOS staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown.](http://images.novusbio.com/fullsize/iNOS-Antibody-Immunocytochemistry-Immunofluorescence-NB300-605-img0013.jpg)
![Western Blot: iNOS Antibody - BSA Free [NB300-605] - Stimulation of IMA 2.1 cells had no effect on relative survival after viral infection. IMA 2.1 cells were stimulated with LPS (10 µg/ml), IFN-gamma , (10 ng/ml) LPS + IFN-gamma , IL-4 (10 ng/ml), FGF (5 ng/ml) or FGF + LPS for 24 h in medium with 2% FBS. Polarization of cells was analyzed by Griess assay (a), Western blot (b) & FACS analysis by detection of MHCII+ cells (c). d MTT assay was performed to detect the relative percentage of VACV-mediated cell death in the presence of stimulating factors. e Viral replication was analyzed by standard plaque assay in the presence of stimulating factors. All experiments were performed in triplicate. Image collected & cropped by CiteAb from the following publication (//www.translational-medicine.com/content/13/1/216), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb300-605_rabbit-polyclonal-inos-antibody-310202415371975.jpg)
![Immunocytochemistry/ Immunofluorescence: iNOS Antibody - BSA Free [NB300-605] - Nfix is mainly expressed by anti-inflammatory MPs. (a) Percentage of F4/80+ MPs positive for Nfix in Tibialis Anterior muscles (TA) of WT mice injected by CTX at D2, D4 & D7, post-injury. Immunostaining for F4/80 (green), Nfix (red) & DAPI (blue) at D4 & D7 after CTX injection; (b) Percentage of Ly6C+ & Ly6C- sorted MPs positive for Nfix in TA muscles of WT mice injected by CTX at D2, D4 & D7 post-injury; (c) Percentage of Nfix+ MPs after M1 & M2c polarization (with IFN gamma & IL10, respectively). * p < 0.05; *** p < 0.001; for (b) * p < 0.05 Ly6C+ vs. Ly6C+ at D4 & D7; # p < 0.05 Ly6C− D7 vs. D2. Results are means ± SEM of at least three independent experiments. Scale bar = 50 μm. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/32183151), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb300-605_rabbit-polyclonal-inos-antibody-31020241517136.jpg)
![Western Blot: iNOS Antibody - BSA Free [NB300-605] - Indolepropionic acid (IPA) induced oxidative stress, cellular energy stress, & decreased the proportions of cancer stem cells. 500,000 cells/well 4T1 cells were treated with IPA in the concentrations indicated for 24 h; then, (A) lipid peroxidation was measured by TBARS assay, & (B) 4HNE expression was assessed by Western blotting (representative figure, n = 3). In the same cells (C), the protein expression of NRF2 (at 68 kDa) & iNOS were determined by Western blotting (n = 3), while (D) the mRNA expression of catalase (cat) was determined by RT-qPCR (n = 3). (E) The expression of the indicated proteins (pACC, ACC, FOXO1, & PGC-1 beta ) were determined by Western blotting (n = 3, except for PGC-1 beta , where n = 2). (F) 100,000 cells/well 4T1 cells were treated with the indicated concentration of IPA for 24 h; then, the proportions of aldehyde dehydrogenase-positive cells were determined in Aldefluor assays using flow cytometry (n = 3). For Western blots, a typical experiment was displayed. Fold data were log2 transformed to achieve normal distribution. Statistical significance was determined using the ANOVA test followed by Dunnett’s post-hoc test, except for panel F, where Student’s t-test was used. * & *** indicate statistically significant difference between control & treated samples at p < 0.05 & p < 0.001, respectively. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/32854297), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb300-605_rabbit-polyclonal-inos-antibody-310202416175250.jpg)
![Western Blot: iNOS Antibody - BSA Free [NB300-605] - NRF2 activation modulated LCA-induced oxidative stress responses in 4T1 breast cancer cells. The 4T1 cells were treated with 0.3 μm LCA & the NRF2 activator RA839 or tBHQ in the concentrations indicated for 48 h. Lipid peroxidation was determined by measuring (A) TBARS (n = 4) & (B,C) 4-HNE levels using western blotting (n = 3). (D) The 4T1 cells were treated with LCA (0.3 μm) and/or GSH & NAC (both at 5 mm) antioxidants for 48 h, then total protein concentration was determined using the sulforhodamine B assay (n = 3). For statistical analysis ANOVA test was used followed by the Dunnett post-hoc test, where all groups were compared to the LCA-treated cohort. Data are plotted as mean ± SEM. ** p < 0.01, LCA vs. LCA/NRF2-activator-treated groups (GSH, reduced glutathione; LCA, lithocholic acid; NAC, N-acetylcysteine; TBARS, thiobarbituric acid reactive substances; 4HNE, 4-hydroxynonenal). Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31461945), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb300-605_rabbit-polyclonal-inos-antibody-31020241616373.jpg)
![Western Blot: iNOS Antibody - BSA Free [NB300-605] - Impaired amount of virus progeny after stimulation of BV-2 cells with IFN-gamma or IFN-gamma & LPS. BV-2 cells were stimulated with LPS (10 µg/ml), IFN-gamma , (10 ng/ml), LPS + IFN-gamma or IL-4 (10 ng/ml) for 24 h in medium with 2% FBS. Polarization of cells was analyzed by Griess assay (a), Western blot (b) & by detection of the percentage of MHCII+ cells by FACS analysis (c). The amount of virus progeny (pfu/ml) was analyzed by standard plaque assay in the presence of stimulating factors & in normal growth medium in cells & supernatants (d). Statistical analysis was performed related to infection medium. To analyze the recovery of viral replication, normal growth medium was applied after infection of pre-stimulated cells. Standard plaque assay was performed to determine viral progeny in cells & supernatant after 24, 48, 72 & 96 hpi (e). To analyze the relative survival of the cells in the presence of stimulating factors a MTT assay was performed (f). The cellular density of stimulated cells relative to unstimulated (w/o) cells was detected via optical density measurement after 24 & 48 h of cultivation (g). Two-sided t test with unequal variances was used for statistics *p < 0.05, **p < 0.01, ***p < 0.001. Active replication was defined as virus titer above the virus titer of the infection medium (red line). All experiments were performed in triplicate & repeated in an independent experiment. Image collected & cropped by CiteAb from the following publication (//www.translational-medicine.com/content/13/1/216), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb300-605_rabbit-polyclonal-inos-antibody-310202416175240.jpg)
![Western Blot: iNOS Antibody - BSA Free [NB300-605] - Inhibitory effect of MMPP on amyloidogenesis & STAT3 translocation in astrocytes & microglia cells. The expression of APP, BACE1 & C99 was detected by Western blotting using specific antibodies in astrocytes (a) & microglia cells (b). Each blot is representative of three experiments. The activity of beta -secretase was investigated using assay kit in astrocytes (c) & microglia cells (d). Values are presented as mean ± S.D. of the three independent experiments performed in triplicate. #p < 0.05 compared to control, *p < 0.05 compared to LPS. Iba-1, COX-2, & iNOS proteins were detected by Western blotting using specific antibodies in astrocytes (e) & microglia cells (f). NO level was measured in astrocytes (g) & microglia cells (h). Activation of STAT3 was investigated using EMSA in astrocytes (i) microglial cells (j) were determined & the expression of STAT3 & phopho-STAT3 was also detected by Western blotting using specific antibodies (k), (l). For the cropped images, samples were run in the same gels under same experimental conditions & processed in parallel. Each band is representative for three experiments Image collected & cropped by CiteAb from the following publication (//link.springer.com/10.1007/s12017-017-8469-3), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb300-605_rabbit-polyclonal-inos-antibody-310202416163790.jpg)
![Western Blot: iNOS Antibody (4E5) [NBP2-22119] - Analysis using iNOS mouse mAb against Jurkat (1), Jurkat (2), A549 (3), HeLa (4), NIH3T3 (5) and MCF-7 (6) cell lysate.](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-Western-Blot-NBP2-22119-img0007.jpg "Western Blot: iNOS Antibody (4E5) [NBP2-22119] - Analysis using iNOS mouse mAb against Jurkat (1), Jurkat (2), A549 (3), HeLa (4), NIH3T3 (5) and MCF-7 (6) cell lysate.")
![Immunohistochemistry-Paraffin: iNOS Antibody (4E5) [NBP2-22119] - Analysis of paraffin-embedded breast cancer tissues using iNOS mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-Immunohistochemistry-Paraffin-NBP2-22119-img0006.jpg)
![Flow Cytometry: iNOS Antibody (4E5) [NBP2-22119] - An intracellular stain was performed on A549 cells with NBP2-22119APC (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated with antibody at 1 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to allophycocyanin (APC).](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-Flow-Cytometry-NBP2-22119-img0011.jpg)
![Flow Cytometry: iNOS Antibody (4E5) [NBP2-22119] - An intracellular stain was performed on A549 cells with NBP2-22119PE (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated with antibody at 2.5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to phycoerythrin (PE).](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-Flow-Cytometry-NBP2-22119-img0010.jpg)
![Western Blot: iNOS Antibody (4E5) [NBP2-22119] - Analysis using iNOS mAb against human iNOS (AA: 997-1058) recombinant protein. (Expected MW is 32.6 kDa)](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-Western-Blot-NBP2-22119-img0002.jpg)
![Flow Cytometry: iNOS Antibody (4E5) - BSA Free [NBP2-22119] - An intracellular stain was performed on NIH3T3 cells with iNOS Antibody (4E5) NBP2-22119 (blue) and a matched isotype control MAB002 (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 1 ug/mL for 30 minutes at room temperature, followed by Mouse IgG (H+L) Cross-Adsorbed Secondary Antibody, Dylight 550 (84540, Thermo Fisher).](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-BSA-Free-Flow-Cytometry-NBP2-22119-img0013.jpg)
![Immunohistochemistry-Paraffin: iNOS Antibody (4E5) [NBP2-22119] - Analysis of paraffin-embedded liver cancer tissues using iNOS mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-Immunohistochemistry-Paraffin-NBP2-22119-img0009.jpg)
![Flow Cytometry: iNOS Antibody (4E5) - BSA Free [NBP2-22119] - An intracellular stain was performed on Caco-2 cells with iNOS Antibody (4E5) NBP2-22119 (blue) and a matched isotype control MAB002 (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 1 ug/mL for 30 minutes at room temperature, followed by Mouse IgG (H+L) Cross-Adsorbed Secondary Antibody, Dylight 550 (84540, Thermo Fisher).](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-BSA-Free-Flow-Cytometry-NBP2-22119-img0012.jpg)
![ELISA: iNOS Antibody (4E5) [NBP2-22119] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng).](http://images.novusbio.com/fullsize/iNOS-Antibody-4E5-ELISA-NBP2-22119-img0001.jpg)
![Immunohistochemistry-Paraffin: iNOS Antibody (K13-A) [NBP1-33780] - Liver tissue stained with anti-iNOS antibody shows strong positive immunostaining of hepatocytes. Formalin fixed, paraffin embedded human tissues (4 um sections) stained according to IHC-P Protocol for NBP1-33780.](http://images.novusbio.com/fullsize/iNOS-Antibody-K13-A-Immunohistochemistry-Paraffin-NBP1-33780-img0011.jpg "Immunohistochemistry-Paraffin: iNOS Antibody (K13-A) [NBP1-33780] - Liver tissue stained with anti-iNOS antibody shows strong positive immunostaining of hepatocytes. Formalin fixed, paraffin embedded human tissues (4 um sections) stained according to IHC-P Protocol for NBP1-33780.")
![Immunohistochemistry-Paraffin: iNOS Antibody (K13-A) [NBP1-33780] - Lung adenocarcinoma tissue stained with anti-iNOS antibody shows strong positive immunostaining of hepatocytes. Formalin fixed, paraffin embedded human tissues (4 um sections) stained according to IHC-P Protocol for NBP1-33780.](http://images.novusbio.com/fullsize/iNOS-Antibody-K13-A-Immunohistochemistry-Paraffin-NBP1-33780-img0012.jpg)
![Immunohistochemistry-Paraffin: iNOS Antibody (K13-A) [NBP1-33780] - Inflamed porcine intestine. Antibody dilution 1:200, overnight 4C. Secondary anti-rabbit Alexa 488 (1:1000) 2 hr incubation. Image from verified customer review.](http://images.novusbio.com/fullsize/iNOS-Antibody-K13-A-Immunohistochemistry-Paraffin-NBP1-33780-img0010.jpg)
![Western Blot: iNOS Antibody (K13-A) [NBP1-33780] - Effects of omega-3 supplementation on the immunocontent of macrophages M1 markers: nitric oxide synthase 2 (NOS-2) (A) & CD86 (B), & M2 marker: Arginase-1 (C) on the mouse paw muscle 48 h after the model induction in Saline/Sham, Saline/CPIP, Omega-3/CPIP, & Corn oil/CPIP groups. Data are expressed as mean ± SD of 6 animals per group, statistically assessed by the one-way ANOVA followed by Tukey’s test. ##p < 0.01 vs. the Saline/Sham group. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/35391753), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nbp1-33780_rabbit-monoclonal-inos-antibody-k13-a-31020241535639.jpg)
![Western Blot: Catalase Antibody (1B8) [NBP2-00492] Analysis of extracts (35ug) from 9 different cell lines by using anti-Catalase monoclonal antibody.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Western-Blot-NBP2-00492-img0015.jpg "Western Blot: Catalase Antibody (1B8) [NBP2-00492] Analysis of extracts (35ug) from 9 different cell lines by using anti-Catalase monoclonal antibody.")
![Immunocytochemistry/Immunofluorescence: Catalase Antibody (OTI1B8) [NBP2-00492] - Mouse hepatocytes stained with catalase antibody. ICC/IF image submitted by a verified customer review.](http://images.novusbio.com/fullsize/Catalase-Antibody-OTI1B8-Immunocytochemistry-Immunofluorescence-NBP2-00492-img0019.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody (1B8) [NBP2-00492] - Staining of paraffin-embedded Human lung tissue using anti-Catalase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Immunohistochemistry-Paraffin-NBP2-00492-img0010.jpg)
![Flow Cytometry: Catalase Antibody (1B8) [NBP2-00492] - Analysis of Jurkat cells, using anti-Catalase antibody, (Red), compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Flow-Cytometry-NBP2-00492-img0017.jpg)
![Western Blot: Catalase Antibody (1B8) [NBP2-00492] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Catalase (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-Catalase.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Western-Blot-NBP2-00492-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: Catalase Antibody (1B8) [NBP2-00492] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY Catalase.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Immunocytochemistry-Immunofluorescence-NBP2-00492-img0018.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody (1B8) [NBP2-00492] - Staining of paraffin-embedded Adenocarcinoma of Human endometrium tissue using anti-Catalase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Immunohistochemistry-Paraffin-NBP2-00492-img0004.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody (1B8) [NBP2-00492] - Staining of paraffin-embedded Carcinoma of Human thyroid tissue using anti-Catalase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Immunohistochemistry-Paraffin-NBP2-00492-img0006.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody (1B8) [NBP2-00492] - Staining of paraffin-embedded Human endometrium tissue using anti-Catalase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Immunohistochemistry-Paraffin-NBP2-00492-img0007.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody (1B8) [NBP2-00492] - Staining of paraffin-embedded Human liver tissue using anti-Catalase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Immunohistochemistry-Paraffin-NBP2-00492-img0009.jpg)
![Flow Cytometry: Catalase Antibody (1B8) [NBP2-00492] - Analysis of Hela cells, using anti-Catalase antibody, (Red), compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/Catalase-Antibody-1B8-Flow-Cytometry-NBP2-00492-img0016.jpg)
![Western Blot: CBS Antibody [NBP1-33518] - Wild-type (WT) and CBS knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CBS-Antibody-Western-Blot-NBP1-33518-img0009.jpg "<b>Genetic Strategies Validation. </b>Western Blot: CBS Antibody [NBP1-33518] - Wild-type (WT) and CBS knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Western Blot: CBS Antibody [NBP1-33518] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody](http://images.novusbio.com/fullsize/CBS-Antibody-Western-Blot-NBP1-33518-img0010.jpg)
![Western Blot: CBS Antibody [NBP1-33518] - Whole cell extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CBS-Antibody-Western-Blot-NBP1-33518-img0015.jpg)
![Immunohistochemistry-Paraffin: CBS Antibody [NBP1-33518] - OVCAR3 xenograft , using CBS antibody at 1:500 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/CBS-Antibody-Immunohistochemistry-Paraffin-NBP1-33518-img0004.jpg)
![Western Blot: CBS Antibody [NBP1-33518] - Mouse tissue extracts (50 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody diluted by 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CBS-Antibody-Western-Blot-NBP1-33518-img0008.jpg)
![Western Blot: CBS Antibody [NBP1-33518] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CBS-Antibody-Western-Blot-NBP1-33518-img0012.jpg)
![Immunoprecipitation: CBS Antibody [NBP1-33518] - CBS antibody immunoprecipitates CBS protein in IP experiments. IP samples: HepG2 whole cell extract. A. 50 ug HepG2 whole cell extract. B. Control with 4 ug of preimmune Rabbit IgG. C. Immunoprecipitation of CBS protein by 4 ug CBS antibody. 7.5 % SDS-PAGE. The immunoprecipitated CBS protein was detected by CBS antibody diluted at 1:500.](http://images.novusbio.com/fullsize/CBS-Antibody-Immunoprecipitation-NBP1-33518-img0014.jpg)
![Immunohistochemistry-Paraffin: CBS Antibody [NBP1-33518] - CBS antibody detects CBS protein at cytoplasm and nucleus by immunohistochemical analysis.Sample: Paraffin-embedded mouse kidney.CBS stained by CBS antibody (NBP1-33518) diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp1-33518_rabbit-polyclonal-cbs-antibody-91020242075953.jpg)
![Immunocytochemistry/ Immunofluorescence: CBS Antibody [NBP1-33518] - CBS antibody detects CBS protein at cytoplasm and nucleus by immunofluorescent analysis.Sample: HeLa cells were fixed in ice-cold MeOH for 5 min.Green: CBS stained by CBS antibody (NBP1-33518) diluted at 1:500.Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] diluted at 1:1000.Blue: Fluoroshield with DAPI .Scale bar= 10um.](http://images.novusbio.com/fullsize/nbp1-33518_rabbit-polyclonal-cbs-antibody-91020242021986.jpg)
![Western Blot: CBS Antibody (519) [NBP2-43604] - Wild-type (WT) and CBS knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody [GT519]. HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CBS-Antibody-519-Western-Blot-NBP2-43604-img0007.jpg "<b>Genetic Strategies Validation. </b>Western Blot: CBS Antibody (519) [NBP2-43604] - Wild-type (WT) and CBS knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody [GT519]. HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Western Blot: CBS Antibody (519) [NBP2-43604] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody (519) diluted at 1:1000. HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CBS-Antibody-519-Western-Blot-NBP2-43604-img0008.jpg)
![Immunohistochemistry-Paraffin: CBS Antibody (519) [NBP2-43604] - Paraffin-embedded mouse kidney. CBS antibody [519] diluted at 1:250.](http://images.novusbio.com/fullsize/CBS-Antibody-519-Immunohistochemistry-Paraffin-NBP2-43604-img0006.jpg)
![Western Blot: CBS Antibody (519) [NBP2-43604] - Analysis of A. 30 ug Raji whole cell lysate/extract B. 30 ug K562 whole cell lysate/extract 7.5 % SDS-PAGE CBS antibody [519] dilution: 1:1000](http://images.novusbio.com/fullsize/CBS-Antibody-519-Western-Blot-NBP2-43604-img0001.jpg)
![Western Blot: CBS Antibody (519) [NBP2-43604] - Analysis of A. 50 ug mouse liver lysate/extract 7.5 % SDS-PAGE CBS antibody [519] dilution: 1:2000.](http://images.novusbio.com/fullsize/CBS-Antibody-519-Western-Blot-NBP2-43604-img0002.jpg)
![Western Blot: CBS Antibody (519) [NBP2-43604] - Analysis of A. 50 ug rat liver lysate/extract 7.5 % SDS-PAGE CBS antibody [519] dilution: 1:1000](http://images.novusbio.com/fullsize/CBS-Antibody-519-Western-Blot-NBP2-43604-img0003.jpg)
![Immunohistochemistry-Paraffin: CBS Antibody (519) [NBP2-43604] - Paraffin-embedded rat liver. CBS antibody [519] diluted at 1:250.](http://images.novusbio.com/fullsize/CBS-Antibody-519-Immunohistochemistry-Paraffin-NBP2-43604-img0005.jpg)
![Various tissue extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody [GT519] (NBP2-43604) diluted at 1:1000. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-43604_mouse-monoclonal-cbs-antibody-519-western-blot-2611202518425420.jpg)
![<b>Genetic Strategies Validation. </b>Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CBS antibody [GT519] (NBP2-43604) diluted at 1:500.](http://images.novusbio.com/fullsize/nbp2-43604_mouse-monoclonal-cbs-antibody-519-western-blot-261120251832450.jpg)
![Western Blot: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Mannose Phosphate Isomerase (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-Mannose Phosphate Isomerase.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Western-Blot-NBP2-02043-img0002.jpg "Western Blot: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Mannose Phosphate Isomerase (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-Mannose Phosphate Isomerase.")
![Immunocytochemistry/Immunofluorescence: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] Staining of COS7 cells transiently transfected by pCMV6-ENTRY Mannose Phosphate Isomerase.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunocytochemistry-Immunofluorescence-NBP2-02043-img0009.jpg)
![Immunohistochemistry-Paraffin: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - Staining of paraffin-embedded Human prostate tissue using anti-Mannose Phosphate Isomerase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunohistochemistry-Paraffin-NBP2-02043-img0008.jpg)
![Flow Cytometry: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - HEK293T cells transfected with either overexpression plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-Mannose Phosphate Isomerase antibody, and then analyzed by flow cytometry.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Flow-Cytometry-NBP2-02043-img0001.jpg)
![Immunohistochemistry-Paraffin: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - Staining of paraffin-embedded Adenocarcinoma of Human endometrium tissue using anti-Mannose Phosphate Isomerase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunohistochemistry-Paraffin-NBP2-02043-img0003.jpg)
![Immunohistochemistry-Paraffin: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - Staining of paraffin-embedded Adenocarcinoma of Human ovary tissue using anti-Mannose Phosphate Isomerase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunohistochemistry-Paraffin-NBP2-02043-img0004.jpg)
![Immunohistochemistry-Paraffin: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - Staining of paraffin-embedded Carcinoma of Human kidney tissue using anti-Mannose Phosphate Isomerase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunohistochemistry-Paraffin-NBP2-02043-img0005.jpg)
![Immunohistochemistry-Paraffin: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - Staining of paraffin-embedded Carcinoma of Human thyroid tissue using anti-Mannose Phosphate Isomerase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunohistochemistry-Paraffin-NBP2-02043-img0006.jpg)
![Immunohistochemistry-Paraffin: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - Staining of paraffin-embedded Human pancreas tissue using anti-Mannose Phosphate Isomerase mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-1C7-Immunohistochemistry-Paraffin-NBP2-02043-img0007.jpg)
![Western Blot: CBS Antibody (1R2E9) [NBP3-15413] - Western blot analysis of extracts of various cell lines, using CBS Rabbit mAb (NBP3-15413) 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: 1s.](http://images.novusbio.com/fullsize/CBS-Antibody-1R2E9-Western-Blot-NBP3-15413-img0004.jpg "Western Blot: CBS Antibody (1R2E9) [NBP3-15413] - Western blot analysis of extracts of various cell lines, using CBS Rabbit mAb (NBP3-15413) 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: 1s.")
![Immunocytochemistry/Immunofluorescence: CBS Antibody (1R2E9) [NBP3-15413] - Immunofluorescence analysis of HeLa cells using CBS Rabbit mAb (NBP3-15413) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/CBS-Antibody-1R2E9-Immunocytochemistry-Immunofluorescence-NBP3-15413-img0003.jpg)
![Immunohistochemistry-Paraffin: CBS Antibody (1R2E9) [NBP3-15413] - Immunohistochemistry of paraffin-embedded human thyroid cancer using CBS Rabbit mAb (NBP3-15413) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/CBS-Antibody-1R2E9-Immunohistochemistry-Paraffin-NBP3-15413-img0002.jpg)
![Western Blot: CBS Antibody (1R2E9) [NBP3-15413] - Western blot analysis of extracts of various cell lines, using CBS Rabbit mAb (NBP3-15413) 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: 30s.](http://images.novusbio.com/fullsize/CBS-Antibody-1R2E9-Western-Blot-NBP3-15413-img0005.jpg)
![Immunohistochemistry-Paraffin: CBS Antibody (1R2E9) [NBP3-15413] - Immunohistochemistry of paraffin-embedded rat lung using CBS Rabbit mAb (NBP3-15413) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/CBS-Antibody-1R2E9-Immunohistochemistry-Paraffin-NBP3-15413-img0001.jpg)
![Immunohistochemistry: CBS Antibody (1R2E9) [CBS] - Immunohistochemistry analysis of paraffin-embedded Human breast cancer tissue using CBS Rabbit mAb at a dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-15413_rabbit-cbs-mab-1r2e9-5220251718926.jpg)
![Immunohistochemistry: CBS Antibody (1R2E9) [CBS] - Immunohistochemistry analysis of paraffin-embedded Human pancreas tissue using CBS Rabbit mAb at a dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-15413_rabbit-cbs-mab-1r2e9-52202517162331.jpg)
![Immunohistochemistry: CBS Antibody (1R2E9) [CBS] - Immunohistochemistry analysis of paraffin-embedded Human kidney tissue using CBS Rabbit mAb at a dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-15413_rabbit-cbs-mab-1r2e9-52202517251980.jpg)
![Immunohistochemistry: CBS Antibody (1R2E9) [CBS] - Immunohistochemistry analysis of paraffin-embedded Human liver tissue using CBS Rabbit mAb at a dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-15413_rabbit-cbs-mab-1r2e9-52202517202912.jpg)
![Western Blot: Catalase Antibody [NBP2-38772] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10. Lane 2: Human cell line RT-4. Lane 3: Human cell line U-251MG. Lane 4: Human Plasma. Lane 5: Human liver tissue](http://images.novusbio.com/fullsize/Catalase-Antibody-Western-Blot-NBP2-38772-img0003.jpg "Western Blot: Catalase Antibody [NBP2-38772] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10. Lane 2: Human cell line RT-4. Lane 3: Human cell line U-251MG. Lane 4: Human Plasma. Lane 5: Human liver tissue")
![Immunocytochemistry/Immunofluorescence: Catalase Antibody [NBP2-38772] - Immunofluorescent staining of human cell line PC-3 shows localization to vesicles.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-38772-img0004.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining of human pancreas using Anti-CAT antibody NBP2-38772.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0011.jpg)
![Immunohistochemistry: Catalase Antibody [NBP2-38772] - Staining of human liver shows strong cytoplasmic positivity in hepatocytes.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-NBP2-38772-img0002.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining of human pancreas shows low expression as expected.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0005.jpg)
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining in human liver and pancreas tissues using anti-CAT antibody. Corresponding CAT RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0006.jpg)
![<b>Independent Antibodies Validation. </b>Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining of human bone marrow, liver, lymph node and pancreas using Anti-CAT antibody NBP2-38772 (A) shows similar protein distribution across tissues to independent antibody NBP2-38646 (B).](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0007.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining of human bone marrow.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0008.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining of human lymph node.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0009.jpg)
![Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-38772] - Staining of human liver using Anti-CAT antibody NBP2-38772.](http://images.novusbio.com/fullsize/Catalase-Antibody-Immunohistochemistry-Paraffin-NBP2-38772-img0010.jpg)
![Western Blot: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Mannose Phosphate.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Western-Blot-NBP2-45834-img0015.jpg "Western Blot: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Mannose Phosphate.")
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Human breast tissue . (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0013.jpg)
![Flow Cytometry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Hela cells, using MPI antibody (Red), compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Flow-Cytometry-NBP2-45834-img0001.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Human tonsil within the normal limits using MPI mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0002.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Adenocarcinoma of Human endometrium tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0003.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Human endometrium tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0004.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Carcinoma of Human kidney tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0005.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Adenocarcinoma of Human ovary tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0006.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Carcinoma of Human thyroid tissue.](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0007.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Human Kidney tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0008.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Carcinoma of Human prostate tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0009.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Human colon tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0010.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Human liver tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0011.jpg)
![Immunohistochemistry: Mannose Phosphate Isomerase Antibody (OTI4G7) [NBP2-45834] - Analysis of Carcinoma of Human lung tissue.(Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/Mannose-Phosphate-Isomerase-Antibody-OTI4G7-Immunohistochemistry-NBP2-45834-img0012.jpg)
![Western Blot: Cytochrome p450 2J2 Antibody (2D10) [H00001573-M01] - analysis of CYP2J2 expression in transfected 293T cell line by CYP2J2 monoclonal antibody (M01), clone 2D10. Lane 1: CYP2J2 transfected lysate (58 KDa). Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/Cytochrome-p450-2J2-Antibody-2D10-Western-Blot-H00001573-M01-img0003.jpg "Western Blot: Cytochrome p450 2J2 Antibody (2D10) [H00001573-M01] - analysis of CYP2J2 expression in transfected 293T cell line by CYP2J2 monoclonal antibody (M01), clone 2D10. Lane 1: CYP2J2 transfected lysate (58 KDa). Lane 2: Non-transfected lysate.")
![Western Blot: Cytochrome p450 2J2 Antibody (2D10) [H00001573-M01] - CYP2J2 monoclonal antibody (M01), clone 2D10 Western Blot analysis of CYP2J2 expression in HepG2 ( Cat # L019V1 ).](http://images.novusbio.com/fullsize/Cytochrome-p450-2J2-Antibody-2D10-Western-Blot-H00001573-M01-img0002.jpg)
![ELISA: Cytochrome p450 2J2 Antibody (2D10) [H00001573-M01] - Detection limit for recombinant GST tagged CYP2J2 is approximately 3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/Cytochrome-p450-2J2-Antibody-2D10-ELISA-H00001573-M01-img0006.jpg)
![Western Blot: FAAH Antibody (4H8) [H00002166-M07] - Analysis of FAAH expression in rat brain.](http://images.novusbio.com/fullsize/FAAH-Antibody-4H8-Western-Blot-H00002166-M07-img0008.jpg "Western Blot: FAAH Antibody (4H8) [H00002166-M07] - Analysis of FAAH expression in rat brain.")
![Western Blot: FAAH Antibody (4H8) [H00002166-M07] - Analysis of FAAH expression in PC-12 (Cat # L012V1).](http://images.novusbio.com/fullsize/FAAH-Antibody-4H8-Western-Blot-H00002166-M07-img0005.jpg)
![Western Blot: FAAH Antibody (4H8) [H00002166-M07] - Analysis of FAAH expression in A-431 (Cat # L015V1).](http://images.novusbio.com/fullsize/FAAH-Antibody-4H8-Western-Blot-H00002166-M07-img0006.jpg)
![Western Blot: FAAH Antibody (4H8) [H00002166-M07] - Analysis of FAAH expression in NIH/3T3 (Cat # L018V1).](http://images.novusbio.com/fullsize/FAAH-Antibody-4H8-Western-Blot-H00002166-M07-img0007.jpg)
![ELISA: FAAH Antibody (4H8) [H00002166-M07] - Detection limit for recombinant GST tagged FAAH is approximately 0.03ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/FAAH-Antibody-4H8-ELISA-H00002166-M07-img0004.jpg)