Novus Biologicals offers 65+ different antibody sampler packs covering a variety of research areas and pathways, allowing researchers to test a panel of similarly targeted antibodies before choosing the ones best suited for their experiment. Our antibody packs are pre-selected and include a variety of popular targets, so you can save time searching for antibodies. Plus, get more antibodies for less! These cost-effective antibody panels let you test sample sizes before buying full-size antibodies. Find the perfect antibody panel for your research by using the filters to easily sort by target, research application, species reactivity, validation, citations, and more.
![Western Blot: Apoptosis Detection Antibody Pack [NBP2-25080] - Image of anti-Caspase 3 (31A1067). Whole cell protein from Jurkat cells treated with and without 2 uM staurosporine as indicated was separated on a 4-15% gel by SDS-PAGE, transferred to 0.2 um PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 5 ug/ml anti-Caspase 3 (NB100-56708) in 1% milk, and detected with an anti-mouse HRP secondary antibody using a Femto sensitivity chemiluminescence reagent. Note the detection of both pro-caspase 3 at 35 kDa and the cleaved active caspase 3 at 15-17 kDa.](http://images.novusbio.com/fullsize/Apoptosis-Detection-Antibody-Pack-Western-Blot-NBP2-25080-img0008.jpg "<b>Biological Strategies Validation. </b>Western Blot: Apoptosis Detection Antibody Pack [NBP2-25080] - Image of anti-Caspase 3 (31A1067). Whole cell protein from Jurkat cells treated with and without 2 uM staurosporine as indicated was separated on a 4-15% gel by SDS-PAGE, transferred to 0.2 um PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 5 ug/ml anti-Caspase 3 (NB100-56708) in 1% milk, and detected with an anti-mouse HRP secondary antibody using a Femto sensitivity chemiluminescence reagent. Note the detection of both pro-caspase 3 at 35 kDa and the cleaved active caspase 3 at 15-17 kDa.")
![<b>Biological Strategies Validation. </b>Western Blot: Apoptosis Detection Antibody Pack [NBP2-25080] - Analysis of Caspase-8 in Jurkat cells using at 1 ug/ml. Cells were treated with 2 uM staurosporine for different time periods. Caspase-8 activation is detected in western blot by the presence of Caspase-8 cleavage fragments. The antibody detected both pro (full-length) and active (cleaved) Caspase-8, depending on the treatment time points. A basal level of endogenously cleaved Caspase-8 can be see in untreated Jurkat cells. this antibody was used in this test.](http://images.novusbio.com/fullsize/Apoptosis-Detection-Antibody-Pack-Western-Blot-NBP2-25080-img0006.jpg)
![Western Blot: Apoptosis Detection Antibody Pack [NBP2-25080] - Analysis of cleaved PARP in staurosporin-treated Jurkat cells at various time points, using at 2 ug/ml. The band corresponding to cleaved PARP is only seen in the treated samples. anti-mouse Ig HRP conjugate was used in this test.](http://images.novusbio.com/fullsize/Apoptosis-Detection-Antibody-Pack-Western-Blot-NBP2-25080-img0007.jpg)
![Flow (Intracellular): N-Cadherin Antibody (13A9) [NBP1-48309] - An intracellular stain was performed on HeLa with NBP1-48309 and a matched isotype control. Cells were fixed with 4% PFA and then permeablized with 0.1% saponin. Cells were incubated in an antibody dilution of 1 ug/mL for 30 minutes at room temperature, followed by Mouse F(ab)2 IgG (H+L) PE-conjugated Antibody.](http://images.novusbio.com/fullsize/nbp3-20202_classical-cadherins-antibody-pack-flow-intracellular-95202311203..jpg)
![Western Blot: LYVE-1 Antibody Pack [NB100-939] - Total protein from human stomach, lymph node and placenta was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 1.0 ug/ml anti-LYVE1 (NB100-725) in 1% milk, and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-Pack-Western-Blot-NB100-939-img0017.jpg "Western Blot: LYVE-1 Antibody Pack [NB100-939] - Total protein from human stomach, lymph node and placenta was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 1.0 ug/ml anti-LYVE1 (NB100-725) in 1% milk, and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.")
![Immunohistochemistry: LYVE-1 Antibody Pack [NB100-939] - Detection of LYVE-1 in endothelial cells of human lung blood vessels using NB100-725. Note presence of RBCs within vessel lumen.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-Pack-Immunohistochemistry-NB100-939-img0004.jpg)
![Western Blot: LYVE-1 Antibody Pack [NB100-939] - Detection of LYVE-1 in mouse spleen lysate using NB 100-726. ECL detection overnight.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-Pack-Western-Blot-NB100-939-img0018.jpg)
![Flow Cytometry: LYVE-1 Antibody Pack [NB100-939] - Analysis using the DyLight 488 conjugate of NB100-725. Unlabeled control with labeled samples of cells dissociated mechanically and enzymatically from human skin. Image provided via product review by Patricia Redondo.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-Pack-Flow-Cytometry-NB100-939-img0019.jpg)
![Immunohistochemistry: LYVE-1 Antibody Pack [NB100-939] - Detection of LYVE-1 in endothelial cells of human lung blood vessels using NB100-725.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-Pack-Immunohistochemistry-NB100-939-img0014.jpg)
![Immunohistochemistry: LYVE-1 Antibody Pack [NB100-939] - Detection of LYVE-1 in endothelial cells of human bladder vasculature using NB100-725.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-Pack-Immunohistochemistry-NB100-939-img0002.jpg)
![Flow Cytometry: TLR Screening Antibody Pack [NBP2-25083] - Expression of TLRs in Fravel, L363, OPM1, RPMI8226, XG1, and NCI-H929 as determined by flow cytometry.HCMLs were stained using an intracellular staining protocol with TLR-specific antibodies followed by relevant secondary fluorescent-conjugated antibodies. Filled histograms (purple) represent the isotype controls and the open histograms (red) indicate specific antibodies. Data are representative for analysis of >=2 independent experiments. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0060671) licensed under a CC-BY license. TLR1 Antibody [NB100-56563], TLR2 Antibody (TL2.1) [NB100-56722], TLR3 Antibody [NBP2-24875], TLR7 Antibody [NBP2-24906], TLR8 Antibody [NBP2-24917], TLR9 Antibody [NBP2-24729]](http://images.novusbio.com/fullsize/TLR-Screening-Antibody-Pack-Flow-Cytometry-NBP2-25083-img0008.jpg "Flow Cytometry: TLR Screening Antibody Pack [NBP2-25083] - Expression of TLRs in Fravel, L363, OPM1, RPMI8226, XG1, and NCI-H929 as determined by flow cytometry.HCMLs were stained using an intracellular staining protocol with TLR-specific antibodies followed by relevant secondary fluorescent-conjugated antibodies. Filled histograms (purple) represent the isotype controls and the open histograms (red) indicate specific antibodies. Data are representative for analysis of >=2 independent experiments. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0060671) licensed under a CC-BY license. TLR1 Antibody [NB100-56563], TLR2 Antibody (TL2.1) [NB100-56722], TLR3 Antibody [NBP2-24875], TLR7 Antibody [NBP2-24906], TLR8 Antibody [NBP2-24917], TLR9 Antibody [NBP2-24729]")
![Immunohistochemistry: TLR Screening Antibody Pack [NBP2-25083] - The expression of TLR-7 in the hippocampal brain region. The immunofluorescence of TLR7 recognized by Alexa 488, green. GFAP recognized by Alexa 594, red. NEUN recognized by Alexa 633, (blue) and merged image in the hippocampal region. NeuN and GFAP were applied to show the distribution of TLR7 within neuronal and supportive tissue populations. Scale bar 80 um. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0222818) licensed under a CC-BY license. TLR7 Antibody [NBP2-24906]](http://images.novusbio.com/fullsize/TLR-Screening-Antibody-Pack-Immunohistochemistry-NBP2-25083-img0007.jpg)
![Western Blot: TLR Screening Antibody Pack [NBP2-25083] - Expression analysis of TLR protein in HMCLs by Western blotting. All cell lines displayed a strong expression of TLR1, TLR3, TLR4, TLR7, TLR9 proteins. Cell lysates were electrophoresed and blotted to PVDF membrane, which was probed with TLR-specific antibodies. To confirm the immunoreactivity of the antibodies, different positive controls were included. Beta-actin was served as loading control and was used to normalize expression levels between cells. Data are representative for analysis of >=2 independent experiments. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0060671) licensed under a CC-BY license. TLR1 Antibody [NB100-56563], TLR3 Antibody [NBP2-24875], TLR7 Antibody [NBP2-24906], TLR9 Antibody [NBP2-24729]](http://images.novusbio.com/fullsize/TLR-Screening-Antibody-Pack-Western-Blot-NBP2-25083-img0009.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: TLR Screening Antibody Pack [NBP2-25083] - Expression of TLR-9 protein in HB cells before and after 48 hr of transfection. Beta-actin was used as an internal control. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0092748) licensed under a CC-BY license. TLR9 Antibody (26C593.2) [NBP2-24729]](http://images.novusbio.com/fullsize/TLR-Screening-Antibody-Pack-Knockout-Validated-NBP2-25083-img0010.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry: TLR Screening Antibody Pack [NBP2-25083] - Representative photographs of immunohistochemistry for tubular TLR2 in G) ctrl, H) ctrl + empa, I) diabetic (dm), J) dm + empagliflozin, K) dm + telmisartan groups (Magnification = original X 200) and quantification of tubular TLR2 expression by Image J (L). (Data are expressed as mean +/- SEM with *=P<0.05 vs ctrl, **=P<0.001 vs ctrl and #=P<0.05 vs dm). Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0108994) licensed under a CC-BY license. TLR2 Antibody [NB100-56720]](http://images.novusbio.com/fullsize/TLR-Screening-Antibody-Pack-Immunohistochemistry-NBP2-25083-img0006.jpg)
![Simple Western: TLR Screening Antibody Pack [NBP2-25083] - Simple Western lane view shows a specific band for TLR8 in 0.5 mg/ml of Ramos (left) and Human Spleen (right) lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system. * Non-specific interaction with the 230 kDa Simple Western standard may be seen with this antibody. TLR8 Antibody (44C143) [NBP2-24917]](http://images.novusbio.com/fullsize/TLR-Screening-Antibody-Pack-Simple-Western-NBP2-25083-img0011.jpg)
![Immunohistochemistry: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Formalin-fixed paraffin-embedded tissue sections of SARS-CoV-2 infected human lung tissue was processed for immunohistochemistry using rabbit polyclonal anti-SARS Nucleocapsid Antibody [NB100-56576] at 15ug/mL with 1 hr incubation at 25 degrees Celsius followed by incubation with anti-rabbit IgG VisUCyte HRP Polymer Antibody [VC003] and DAB chromogen (yellow-brown). Tissue was counterstained with hematoxylin (blue). Specific staining was localized to SARS-CoV-2 infected cells.](http://images.novusbio.com/fullsize/SARS-Nucleocapsid-Protein-Antibody-Pack-Immunohistochemistry-NBP3-05695-img0003.jpg "Immunohistochemistry: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Formalin-fixed paraffin-embedded tissue sections of SARS-CoV-2 infected human lung tissue was processed for immunohistochemistry using rabbit polyclonal anti-SARS Nucleocapsid Antibody [NB100-56576] at 15ug/mL with 1 hr incubation at 25 degrees Celsius followed by incubation with anti-rabbit IgG VisUCyte HRP Polymer Antibody [VC003] and DAB chromogen (yellow-brown). Tissue was counterstained with hematoxylin (blue). Specific staining was localized to SARS-CoV-2 infected cells.")
![Immunocytochemistry/Immunofluorescence: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Immunofluorescence assay using Rabbit Anti-SARS-CoV Nucleocapsid (N) Antibody[NBP2-44205], showing viral protein synthesis. VeroE6 cells were infected with rSARS-CoV-2. Mock: non-infected cells. At 48 h.p.i, cells were fixed and prepared for immunofluorescence staining with primary antibodies directed against double-stranded RNA (dsRNA) [green] and SARS-CoV Nucleocapsid (N) [red]. Nuclear Counterstain DAPI [blue].](http://images.novusbio.com/fullsize/SARS-Nucleocapsid-Protein-Antibody-Pack-Immunocytochemistry-Immunofluorescence-NBP3-05695-img0001.jpg)
![Western Blot: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Analysis of SARS Nucleocapsid in (A) untransfected mouse melanoma cell lysate and (B) transfected cell lysate using this antibody [NB100-56683] at a 1:2000 dilution.](http://images.novusbio.com/fullsize/SARS-Nucleocapsid-Protein-Antibody-Pack-Western-Blot-NBP3-05695-img0004.jpg)
![Western Blot: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Western blot using Protein A Purified anti-SARS CoV Nucleocapsid (N) protein antibody shows detection of a 46 kDa band corresponding to the protein. Approx. 100 ng of protein was loaded for SDS-PAGE and transferred onto nitrocellulose. The blot was incubated with a 1:5,000 dilution of the antibody[NBP2-44205] at room temperature for 1 h followed by detection using IRDy(TM) 800 labeled Goat-a-Rabbit IgG [H&L] diluted 1:10,000. The fluorescence image was captured using the Odyssey(R) Infrared Imaging System developed by LI-COR. IRDye is a trademark of LI-COR, Inc. Other detection systems will yield similar results.](http://images.novusbio.com/fullsize/SARS-Nucleocapsid-Protein-Antibody-Pack-Western-Blot-NBP3-05695-img0006.jpg)
![Immunohistochemistry: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Formalin-fixed paraffin-embedded tissue sections of SARS-CoV-2 infected human lung tissue was processed for immunohistochemistry using rabbit polyclonal anti-SARS Nucleocapsid Antibody [NB100-56683] at 15ug/mL with 1 hr incubation at 25 degrees Celsius followed by incubation with anti-rabbit IgG VisUCyte HRP Polymer Antibody [VC003] and DAB chromogen (yellow-brown). Tissue was counterstained with hematoxylin (blue). Specific staining was localized to SARS-CoV-2 infected cells.](http://images.novusbio.com/fullsize/SARS-Nucleocapsid-Protein-Antibody-Pack-Immunohistochemistry-NBP3-05695-img0005.jpg)
![Immunohistochemistry: SARS Nucleocapsid Protein Antibody Pack [NBP3-05695] - Pathological changes in rhesus macaques infected with SARS-CoV-2. (g) SARSCoV-2 antigen is detected by immunohistochemistry in type I pneumocytes. Magnification 400x. (j) SARS-CoV-2 antigen is detected by immunohistochemistry in type I pneumocytes (asterisk) and type II pneumocytes (arrow) as well as alveolar macrophages (arrowheads). Magnification 400x. (k) SARS-CoV-2 antigen is detected by immunohistochemistry in mediastinal lymph node. Magnification 400x. (l) SARSCoV-2 antigen is detected by immunohistochemistry in macrophages and lymphocytes in the lamina propria of the cecum. Magnification 400x. bioRxiv March 21, 2020 //doi.org/10.1101/2020.03.21.001628 SARS Nucleocapsid Protein Antibody [NB100-56576]](http://images.novusbio.com/fullsize/SARS-Nucleocapsid-Protein-Antibody-Pack-Immunohistochemistry-NBP3-05695-img0002.jpg)
![Western Blot: Panoptosome Antibody Pack [NBP3-20189] - Analysis of RIP3 using polyclonal RIPK3/RIP3 antibody [NBP2-24588]. Human tissue blot probed with 5 ug/ml of RIP3 antibody: 1) brain, 2) heart, 3) small intestine, 4) kidney, 5) liver, 6) lung, 7) skeletal muscle, 8) stomach, 9) spleen, 10) ovary, 11) testis, 12) placenta probed at 5 ug/ml, 13) Ramos cell lysate probed at 7 ug/ml. Theoretical molecular weight 56.7 kDa.](http://images.novusbio.com/fullsize/nbp3-20189_panoptosome-antibody-pack-western-blot-352023125539.jpg "Western Blot: Panoptosome Antibody Pack [NBP3-20189] - Analysis of RIP3 using polyclonal RIPK3/RIP3 antibody [NBP2-24588]. Human tissue blot probed with 5 ug/ml of RIP3 antibody: 1) brain, 2) heart, 3) small intestine, 4) kidney, 5) liver, 6) lung, 7) skeletal muscle, 8) stomach, 9) spleen, 10) ovary, 11) testis, 12) placenta probed at 5 ug/ml, 13) Ramos cell lysate probed at 7 ug/ml. Theoretical molecular weight 56.7 kDa.")
![<b>Genetic Strategies Validation. </b>Western Blot: Panoptosome Antibody Pack [NBP3-20189] - Western blot shows lysates of MCF‑7 human breast cancer parental cell line and RIPK1/RIP1 knockout MCF‑7 cell line (KO). PVDF membrane was probed with 0.5 µg/mL of Mouse Anti-Human/Mouse/Rat RIPK1/RIP1 Monoclonal Antibody (Catalog # MAB3585) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for RIPK1/RIP1 at approximately 75 kDa (as indicated) in the parental MCF‑7 cell line, but is not detectable in knockout MCF‑7 cell line. GAPDH (Catalog # MAB5718) is shown as a loading control. This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.](http://images.novusbio.com/fullsize/nbp3-20189_panoptosome-antibody-pack-knockout-validated-352023125740.jpg)
![Flow (Intracellular): Panoptosome Antibody Pack [NBP3-20189] - An intracellular stain was performed on MCF7 cells with ASC/TMS1 NBP1-78977 (blue) and a matched isotype control NBP2-24891 (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 Rabbit IgG (H+L) Cross-Adsorbed Secondary Antibody, Dylight 550 (SA5-10033, Thermo Fisher).](http://images.novusbio.com/fullsize/nbp3-20189_panoptosome-antibody-pack-flow-intracellular-35202313025.jpg)
![Western Blot: Panoptosome Antibody Pack [NBP3-20189] - Analysis of active/cleaved Caspase 8 in NRK whole cell lysate using anti-active/cleaved Caspase 8 antibody (NB100-56116).](http://images.novusbio.com/fullsize/nbp3-20189_panoptosome-antibody-pack-western-blot-35202313819.jpg)
![Immunohistochemistry-Paraffin: Panoptosome Antibody Pack [NBP3-20189] - Immunohistochemistry-Paraffin: Panoptosome Antibody Pack [NBP3-20189] - Analysis of a FFPE tissue section of human stomach using 1:200 dilution of TAK1 antibody (NB100-56363). The staining was developed using HRP labeled anti-rabbit secondary antibody and DAB reagent, and nuclei of cells were counter-stained with hematoxylin](http://images.novusbio.com/fullsize/nbp3-20189_panoptosome-antibody-pack-immunohistochemistry-paraffin-352023131253.jpg)
![Immunohistochemistry: TLR7 Antibody Pack [NBP2-31097] - The expression of TLR-7 in the hippocampal brain region. The immunofluorescence of TLR7 recognized by Alexa 488, green. GFAP recognized by Alexa 594, red. NEUN recognized by Alexa 633, (blue) and merged image in the hippocampal region. NeuN and GFAP were applied to show the distribution of TLR7 within neuronal and supportive tissue populations. Scale bar 80 um. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0222818) licensed under a CC-BY license. TLR7 Antibody [NBP2-24906]](http://images.novusbio.com/fullsize/TLR7-Antibody-Pack-Immunohistochemistry-NBP2-31097-img0002.jpg "Immunohistochemistry: TLR7 Antibody Pack [NBP2-31097] - The expression of TLR-7 in the hippocampal brain region. The immunofluorescence of TLR7 recognized by Alexa 488, green. GFAP recognized by Alexa 594, red. NEUN recognized by Alexa 633, (blue) and merged image in the hippocampal region. NeuN and GFAP were applied to show the distribution of TLR7 within neuronal and supportive tissue populations. Scale bar 80 um. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0222818) licensed under a CC-BY license. TLR7 Antibody [NBP2-24906]")
![Flow Cytometry: TLR7 Antibody Pack [NBP2-31097] - An intracellular stain was performed on THP-1 cells with NBP2-24906 (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 5.0 ug/mL for 30 minutes at room temperature, followed by Rabbit IgG (H+L) Cross-Adsorbed Secondary Antibody, Dylight 550. TLR7 Antibody [NBP2-24906]](http://images.novusbio.com/fullsize/TLR7-Antibody-Pack-Flow-Cytometry-NBP2-31097-img0001.jpg)
![Immunohistochemistry: TLR7 Antibody Pack [NBP2-31097] - Sections of nasal biopsies were incubated with antibodies against TLR9 (C) visualized by 3, 3-diaminobenzidine (brown). In control slides (F), N-series universal negative control reagent was used. All sections were accompanied with a square magnification. All slides were counterstained with haematoxylin (blue). The figure shows one representative biopsy out of four (3 male, 1 female). The arrows indicate positive stained cells. Image collected and cropped by CiteAb from the following publication (//doi.org/10.1371/journal.pone.0098239) licensed under a CC-BY license. TLR7 Antibody [NB100-56682]](http://images.novusbio.com/fullsize/TLR7-Antibody-Pack-Immunohistochemistry-NBP2-31097-img0003.jpg)
![Immunohistochemistry: TLR7 Antibody Pack [NBP2-31097] - Human brain using 1:50 dilution of TLR7 antibody on a Bond Rx autostainer (Leica Biosystems). The assay involved 20 minutes of heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0) and endogenous peroxidase quenching with peroxide block. The sections were incubated with primary antibody for 30 minutes and Bond Polymer Refine Detection (Leica Biosystems) with DAB was used for signal development followed by counterstaining with hematoxylin. Whole slide scanning and capturing of representative images (20X) was performed using Aperio AT2 (Leica Biosystems). Punctate staining of neurons was observed. Staining was performed by Histowiz. TLR7 Antibody [NBP2-24767]](http://images.novusbio.com/fullsize/TLR7-Antibody-Pack-Immunohistochemistry-NBP2-31097-img0004.jpg)
![Flow Cytometry: TLR7 Antibody Pack [NBP2-31097] - Intracellular flow analysis of TLR7 in 10^6 ThP1 cells using 2 ug of NB100-56588. Shaded histogram represents cells without antibody. Green: isotype control. Red: TLR7 antibody. Intracellular flow kit was used for this test, and an anti-rabbit IgG PE conjugated secondary. TLR7 Antibody [NB100-56588]](http://images.novusbio.com/fullsize/TLR7-Antibody-Pack-Flow-Cytometry-NBP2-31097-img0005.jpg)
![Immunohistochemistry: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - VN1203 induced significant pathology despite similar nasal turbinate titers in ferrets infected with either virus. Viral titers of homogenized nasal turbinates were graphed as mean +/- SEM for VN1203 or HK483 infected ferrets. D-I. Representative samples of nasal turbinate tissue of ferrets instilled with allantoic fluid (D,G), HK483 (E,H), or VN1203 (F,I). D-F were stained with H&E, G-I were stained with anti-avian influenza NP (NB100-56572) and counterstained with Luxol fast blue. F. # indicates inflammatory cells infiltrating the underlying stroma. H,I. Arrows point to H5N1 infected cells. Scale bars: D-F, 300 um; G-I, 100 um. Image collected and cropped by CiteAb from the following publication (//dx.plos.org/10.1371/journal.pone.0046605) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Immunohistochemistry-NBP2-25066-img0009.jpg "Immunohistochemistry: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - VN1203 induced significant pathology despite similar nasal turbinate titers in ferrets infected with either virus. Viral titers of homogenized nasal turbinates were graphed as mean +/- SEM for VN1203 or HK483 infected ferrets. D-I. Representative samples of nasal turbinate tissue of ferrets instilled with allantoic fluid (D,G), HK483 (E,H), or VN1203 (F,I). D-F were stained with H&E, G-I were stained with anti-avian influenza NP (NB100-56572) and counterstained with Luxol fast blue. F. # indicates inflammatory cells infiltrating the underlying stroma. H,I. Arrows point to H5N1 infected cells. Scale bars: D-F, 300 um; G-I, 100 um. Image collected and cropped by CiteAb from the following publication (//dx.plos.org/10.1371/journal.pone.0046605) licensed under a CC-BY license.")
![Western Blot: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Analysis of avian flu matrix protein 1 in (A) recombinant fusion protein containing amino acids 212-225 and (B) fusion partner without these amino acids, using NB100-56610 at 0.5 ug/ml.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Western-Blot-NBP2-25066-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Staining of influenza-infected MDCK cells using NB100-1933 at 1:10 dilution. Image Courtesy of Catherine Thompson, The University of Reading.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Immunocytochemistry-Immunofluorescence-NBP2-25066-img0007.jpg)
![Western Blot: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Analysis of avian flu HA in (A) recombinant fusion protein containing amino acids 128-143 and (B) fusion partner without these amino acids, using NB100-56608 at 0.5 ug/ml.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Western-Blot-NBP2-25066-img0001.jpg)
![Western Blot: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Analysis of avian flu nucleoprotein in (A) recombinant fusion protein containing amino acids 58-77 and (B) fusion partner without these amino acids, using NB100-56611 at 0.5 ug/ml.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Western-Blot-NBP2-25066-img0003.jpg)
![Western Blot: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Analysis of avian flu HA in (A) recombinant fusion protein containing amino acids 72-88 and (B) fusion partner without these amino acids, using NB100-56607 at 0. 5 ug/ml.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Western-Blot-NBP2-25066-img0004.jpg)
![Western Blot: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Analysis of avian flu matrix protein 1 in (A) recombinant fusion protein containing amino acids 9-28 and (B) fusion partner without these amino acids, using NB100-1933 at 0.5 ug/ml.](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Western-Blot-NBP2-25066-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Staining of influenza-infected MDCK cells using NB100-56608 at 1:10 dilution. Image Courtesy of Catherine Thompson, The University of Reading](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Immunocytochemistry-Immunofluorescence-NBP2-25066-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Avian Influenza A Hemagglutinin Antibody Pack [NBP2-25066] - Staining of influenza-infected MDCK cells with NB100-56572 at 1:10 dilution. Image Courtesy of Catherine Thompson, The University of Reading](http://images.novusbio.com/fullsize/Avian-Influenza-A-Hemagglutinin-Antibody-Pack-Immunocytochemistry-Immunofluorescence-NBP2-25066-img0005.jpg)