| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-89959-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-64831-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-35146-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90452-50ul | |||
![Western Blot: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Western blot analysis of Myeloperoxidase/MPO on different lysates with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/5,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 84 kDa Observed band size: 84/55 kDa Exposure time: 24 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32624) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-2882024142265.jpg "Western Blot: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Western blot analysis of Myeloperoxidase/MPO on different lysates with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/5,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 84 kDa Observed band size: 84/55 kDa Exposure time: 24 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32624) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32624) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-298202414161865.jpg)
![Immunocytochemistry/ Immunofluorescence: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Immunocytochemistry analysis of Jurkat cells labeling Myeloperoxidase/MPO with Rabbit anti-Myeloperoxidase/MPO/MPO antibody (NBP3-32624) at 1/100 dilution. Cells were fixed in 80% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-29202410234294.jpg)
![Immunohistochemistry-Paraffin: Leukotriene B4 R1 Antibody [NBP1-89959] - Staining of human spleen shows strong cytoplasmic positivity in cells in red pulp.](http://images.novusbio.com/fullsize/Leukotriene-B4-R1-Antibody-Immunohistochemistry-Paraffin-NBP1-89959-img0002.jpg "Immunohistochemistry-Paraffin: Leukotriene B4 R1 Antibody [NBP1-89959] - Staining of human spleen shows strong cytoplasmic positivity in cells in red pulp.")
![Flow Cytometry: Leukotriene B4 R1 Antibody (202/7B1) [NB100-64831] - Analysis using the Biotin conjugate of NB100-64831. Staining of human peripheral blood granulocytes.](http://images.novusbio.com/fullsize/Leukotriene-B4-R1-Antibody-202-7B1-Flow-Cytometry-NB100-64831-img0005.jpg "Flow Cytometry: Leukotriene B4 R1 Antibody (202/7B1) [NB100-64831] - Analysis using the Biotin conjugate of NB100-64831. Staining of human peripheral blood granulocytes.")
![Flow Cytometry: Leukotriene B4 R1 Antibody (202/7B1) [NB100-64831] - Staining of human peripheral blood granulocytes with MOUSE ANTI HUMAN BLTR: RPE.](http://images.novusbio.com/fullsize/Leukotriene-B4-R1-Antibody-202-7B1-Flow-Cytometry-NB100-64831-img0002.jpg)
![Flow Cytometry: Leukotriene B4 R1 Antibody (202/7B1) [NB100-64831] - Staining of human peripheral blood granulocytes with MOUSE ANTI HUMAN BLTR: FITC.](http://images.novusbio.com/fullsize/Leukotriene-B4-R1-Antibody-202-7B1-Flow-Cytometry-NB100-64831-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: Goat Polyclonal TREM2 Antibody [NBP1-44067] - Immunofluorescence analysis of paraformaldehyde fixed 3T3-L1 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane/cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).](http://images.novusbio.com/fullsize/antibody/nbp1-44067_goat-polyclonal-trem2-antibody-imgenex-img-31149-immunocytochemistry-immunofluorescence-2832024141818..jpg "Immunocytochemistry/Immunofluorescence: Goat Polyclonal TREM2 Antibody [NBP1-44067] - Immunofluorescence analysis of paraformaldehyde fixed 3T3-L1 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane/cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).")
![Immunocytochemistry/Immunofluorescence: Goat Polyclonal TREM2 Antibody [NBP1-44067] - Immunofluorescence analysis of paraformaldehyde fixed RAW264.7 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).](http://images.novusbio.com/fullsize/antibody/nbp1-44067_goat-polyclonal-trem2-antibody-imgenex-img-31149-immunocytochemistry-immunofluorescence-2832024142259..jpg)
![Immunocytochemistry/ Immunofluorescence: TREM2 Antibody [NBP3-35146] - Immunofluorescence analysis of PC-12 cells using TREM2 Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-35146_rabbit-trem2-pab-1012202411343353.jpg "Immunocytochemistry/ Immunofluorescence: TREM2 Antibody [NBP3-35146] - Immunofluorescence analysis of PC-12 cells using TREM2 Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.")
![Western Blot: TREM2 Antibody [NBP3-35146] - Western Blot analysis of lysates from Rat lung using TREM2 Rabbit pAb at 1:2000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 30s.](http://images.novusbio.com/fullsize/nbp3-35146_rabbit-trem2-pab-311202517313.jpg)
![Western Blot: Leukotriene B4 R1 Antibody (JE58-77) [NBP3-32529] - Western blot analysis of Leukotriene B4 R1 on different lysates with Rabbit anti-Leukotriene B4 R1 antibody (NBP3-32529) at 1/1,000 dilution. Lane 1: MCF7 cell lysate Lane 2: MDA-MB-468 cell lysate (no heat) Lysates/proteins at 20 ug/Lane. Predicted band size: 38 kDa Observed band size: 38 kDa Exposure time: 10 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32529) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32529_rabbit-leukotriene-b4-r1-mab-je58-77-278202415295592.jpg "Western Blot: Leukotriene B4 R1 Antibody (JE58-77) [NBP3-32529] - Western blot analysis of Leukotriene B4 R1 on different lysates with Rabbit anti-Leukotriene B4 R1 antibody (NBP3-32529) at 1/1,000 dilution. Lane 1: MCF7 cell lysate Lane 2: MDA-MB-468 cell lysate (no heat) Lysates/proteins at 20 ug/Lane. Predicted band size: 38 kDa Observed band size: 38 kDa Exposure time: 10 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32529) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Leukotriene B4 R1 Antibody (JE58-77) [NBP3-32529] - Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-Leukotriene B4 R1 antibody (NBP3-32529) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32529) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32529_rabbit-leukotriene-b4-r1-mab-je58-77-29820241433366.jpg)
![Western Blot: Myeloperoxidase/MPO Antibody (RM407) [NBP2-89098] - Western Blot of HL60 cell lysate using Anti-MPO rabbit monoclonal antibody (Clone RM407) at a 1:200 dilution.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-RM407-Western-Blot-NBP2-89098-img0002.jpg "Western Blot: Myeloperoxidase/MPO Antibody (RM407) [NBP2-89098] - Western Blot of HL60 cell lysate using Anti-MPO rabbit monoclonal antibody (Clone RM407) at a 1:200 dilution.")
![Immunohistochemistry-Paraffin: Myeloperoxidase/MPO Antibody (RM407) [NBP2-89098] - Immunohistochemical staining of formalin fixed and paraffin embedded human tonsil tissue section using Anti-MPO Rabbit Monoclonal Antibody (Clone RM407) at a 1:100 dilution.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-RM407-Immunohistochemistry-Paraffin-NBP2-89098-img0001.jpg)
![Immunohistochemistry-Paraffin: Myeloperoxidase/MPO Antibody (RM407) [NBP2-89098] - Immunohistochemical staining of formalin fixed and paraffin embedded human cholangiocarcinoma tissue section using NBP2-89098 at 1:100 dilution.](http://images.novusbio.com/fullsize/nbp2-89098_rabbit-monoclonal-myeloperoxidase-mpo-antibody-rm407-13102023193750.png)
![Flow (Intracellular): Myeloperoxidase/MPO Antibody (MPO421-8B2) [NBP2-41406] - Separation of human neutrophil granulocytes (red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (intracellular staining) of human peripheral whole blood stained using anti-human Myeloperoxidase (MPO421-8B2) purified antibody (concentration in sample 1 ug/ml).](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-MPO421-8B2-Flow-Intracellular-NBP2-41406-img0002.jpg "Flow (Intracellular): Myeloperoxidase/MPO Antibody (MPO421-8B2) [NBP2-41406] - Separation of human neutrophil granulocytes (red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (intracellular staining) of human peripheral whole blood stained using anti-human Myeloperoxidase (MPO421-8B2) purified antibody (concentration in sample 1 ug/ml).")
![Flow (Intracellular): Myeloperoxidase/MPO Antibody (MPO421-8B2) [NBP2-41406] - Intracellular staining pattern of human peripheral whole blood stained using anti-human Myeloperoxidase (MPO421-8B2) purified antibody (concentration in sample 1 ug/ml).](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-MPO421-8B2-Flow-Intracellular-NBP2-41406-img0001.jpg)
![Western Blot: Myeloperoxidase/MPO Antibody (S07-2C7) [NBP3-19707] - Western blot detection of Myeloperoxidase/MPO in 3T3 cell lysates using NBP3-19707 (1:1000 diluted). Predicted band size: 84kDa. Observed band size: 80-90kDa.](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-S07-2C7-Western-Blot-NBP3-19707-img0002.jpg "Western Blot: Myeloperoxidase/MPO Antibody (S07-2C7) [NBP3-19707] - Western blot detection of Myeloperoxidase/MPO in 3T3 cell lysates using NBP3-19707 (1:1000 diluted). Predicted band size: 84kDa. Observed band size: 80-90kDa.")
![Immunohistochemistry-Paraffin: Myeloperoxidase/MPO Antibody (S07-2C7) [NBP3-19707] - Immunohistochemistry of Myeloperoxidase/MPO in paraffin-embedded Human colon cancer tissue using NBP3-19707 at dilution 1/50](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-S07-2C7-Immunohistochemistry-Paraffin-NBP3-19707-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: TREM2 Antibody (014) [NBP2-90452] - Immunofluorescence staining of TREM2 in RAW264.7 cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90452 antibody (dilution ratio 1:60) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG Secondary antibody (green) and counterstained with DAPI (blue).Positive staining was localized to Cytoplasm and cell membrane.](http://images.novusbio.com/fullsize/nbp2-90452_rabbit-monoclonal-trem2-antibody-014-23520251628190.png "Immunocytochemistry/Immunofluorescence: TREM2 Antibody (014) [NBP2-90452] - Immunofluorescence staining of TREM2 in RAW264.7 cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90452 antibody (dilution ratio 1:60) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG Secondary antibody (green) and counterstained with DAPI (blue).Positive staining was localized to Cytoplasm and cell membrane.")