| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90404-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90403-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90685-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89738-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35105-1mg | |||
| Carrier-Free | NBP2-35105-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81084-0.025mg | |||
![Western Blot: Thrombopoietin R/Tpo R Antibody (JE58-00) [NBP3-33039] - Western blot analysis of Thrombopoietin R/Tpo R on different lysates with Rabbit anti-Thrombopoietin R/Tpo R antibody (NBP3-33039) at 1/1,000 dilution. Lane 1: Mouse placenta tissue lysate (40 ug/Lane) Lane 2: NIH/3T3 cell lysate (20 ug/Lane) Lane 3: A431 cell lysate (no heat) (20 ug/Lane) Lane 4: Rat spleen tissue lysate (40 ug/Lane) Lane 5: Mouse spleen tissue lysate (40 ug/Lane) Predicted band size: 71 kDa Observed band size: 80 kDa Exposure time: Lane 1-3: 24 seconds; Lane 4-5: 30 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 (NBP3-33039) at 1/1,000 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/nbp3-33039_rabbit-thrombopoietin-r-tpo-r-mab-je58-00-288202412493457.jpg "Western Blot: Thrombopoietin R/Tpo R Antibody (JE58-00) [NBP3-33039] - Western blot analysis of Thrombopoietin R/Tpo R on different lysates with Rabbit anti-Thrombopoietin R/Tpo R antibody (NBP3-33039) at 1/1,000 dilution. Lane 1: Mouse placenta tissue lysate (40 ug/Lane) Lane 2: NIH/3T3 cell lysate (20 ug/Lane) Lane 3: A431 cell lysate (no heat) (20 ug/Lane) Lane 4: Rat spleen tissue lysate (40 ug/Lane) Lane 5: Mouse spleen tissue lysate (40 ug/Lane) Predicted band size: 71 kDa Observed band size: 80 kDa Exposure time: Lane 1-3: 24 seconds; Lane 4-5: 30 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 (NBP3-33039) at 1/1,000 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.")
![Flow Cytometry: Thrombopoietin R/Tpo R Antibody (JE58-00) [NBP3-33039] - Flow cytometric analysis of A431 cells labeling Thrombopoietin R/Tpo R. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-33039, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-33039_rabbit-thrombopoietin-r-tpo-r-mab-je58-00-29202416372192.jpg)
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse spleen with rabbit monoclonal antibody (1:200). Positive staining was localized to Kupffer cell.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90404-img0003.jpg "Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse spleen with rabbit monoclonal antibody (1:200). Positive staining was localized to Kupffer cell.")
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse brain with rabbit monoclonal antibody (1:200). Positive staining was localized to microglia.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90404-img0001.jpg)
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse liver with rabbit monoclonal antibody (1:100). Positive staining was localized to Kupffer cell.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90404-img0002.jpg)
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (1) [NBP2-90403] - Mouse spleen with rabbit monoclonal antibody (1:200). The left panel: tissue incubated with primary antibody; The right panel: tissue incubated with the mixture of primary antibody and antigen (recombinant protein).](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-1-Immunohistochemistry-Paraffin-NBP2-90403-img0003.jpg "Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (1) [NBP2-90403] - Mouse spleen with rabbit monoclonal antibody (1:200). The left panel: tissue incubated with primary antibody; The right panel: tissue incubated with the mixture of primary antibody and antigen (recombinant protein).")
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (1) [NBP2-90403] - Mouse brain with rabbit monoclonal antibody (1:200). Positive staining was localized to microglia.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-1-Immunohistochemistry-Paraffin-NBP2-90403-img0001.jpg)
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (1) [NBP2-90403] - Mouse liver with rabbit monoclonal antibody (1:200). Positive staining was localized to Kupffer cell.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-1-Immunohistochemistry-Paraffin-NBP2-90403-img0002.jpg)
![Western Blot: PD-L1 Antibody (PSH04-80) [NBP3-32731] - Western blot analysis of PD-L1 on different lysates with Rabbit anti-PD-L1 antibody (NBP3-32731) at 1/2,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 10ug/mL LPS for 8 hours cell lysate Lane 3: J774A.1 cell lysate Lane 4: J774A.1 treated with 1ug/mL LPS for 24 hours cell lysate Lane 5: Mouse spleen tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 33 kDa Observed band size: 45-60 kDa Exposure time: 46 seconds; ECL; 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 (NBP3-32731) at 1/2,000 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/nbp3-32731_rabbit-pd-l1-mab-psh04-80-27820241631671.jpg "Western Blot: PD-L1 Antibody (PSH04-80) [NBP3-32731] - Western blot analysis of PD-L1 on different lysates with Rabbit anti-PD-L1 antibody (NBP3-32731) at 1/2,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 10ug/mL LPS for 8 hours cell lysate Lane 3: J774A.1 cell lysate Lane 4: J774A.1 treated with 1ug/mL LPS for 24 hours cell lysate Lane 5: Mouse spleen tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 33 kDa Observed band size: 45-60 kDa Exposure time: 46 seconds; ECL; 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 (NBP3-32731) at 1/2,000 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: PD-L1 Antibody (PSH04-80) [NBP3-32731] - Immunohistochemical analysis of paraffin-embedded mouse thymus tissue with Rabbit anti-PD-L1 antibody (NBP3-32731) at 1/200 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 (NBP3-32731) at 1/200 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/nbp3-32731_rabbit-pd-l1-mab-psh04-80-29820241433368.jpg)
![Flow Cytometry: Mouse Monoclonal SHIP Antibody (SHIP-02) [NBP1-45077] - Separation of MOLT-4 cells stained using anti-SHIP1 (SHIP-02) purified antibody (concentration in sample 3 μg/ml, GAM APC, red-filled) from MOLT-4 cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).](http://images.novusbio.com/fullsize/antibody/nbp1-45077_mouse-monoclonal-ship-antibody-ship-02-flow-cytometry-11122024125446..jpg "Flow Cytometry: Mouse Monoclonal SHIP Antibody (SHIP-02) [NBP1-45077] - Separation of MOLT-4 cells stained using anti-SHIP1 (SHIP-02) purified antibody (concentration in sample 3 μg/ml, GAM APC, red-filled) from MOLT-4 cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).")
![Western Blot: SHIP Antibody (SHIP-02) [NBP1-45077] - Analysis (reducing conditions) of human SHIP-1 in whole cell lysate of THP-1 human acute monocytic leukemia cell line. Lane 1: immunostaining with Isotype mouse IgG1 control (PPV-04) Lane 2,3: immunostaining with anti-human SHIP-1 (SHIP-01; cat. no. NB110-81538) Lane 4,5: immunostaining with anti-human SHIP-1 (SHIP-02)](http://images.novusbio.com/fullsize/SHIP-Antibody-SHIP-02-Western-Blot-NBP1-45077-img0002.jpg)
![Flow Cytometry: IFN-gamma R1/CD119 Antibody (062) [NBP2-90685] - Flow cytometric analysis of Mouse IFNGR1(CD119) expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse IFNGR1(CD119), then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/IFN-gamma-R1-CD119-Antibody-062-Flow-Cytometry-NBP2-90685-img0002.jpg "Flow Cytometry: IFN-gamma R1/CD119 Antibody (062) [NBP2-90685] - Flow cytometric analysis of Mouse IFNGR1(CD119) expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse IFNGR1(CD119), then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![Immunocytochemistry/ Immunofluorescence: IFN-gamma R1/CD119 Antibody (062) [NBP2-90685] -staining of mouse IFN-gamma R1/CD119 in mouse splenocytes. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90685 (1:60) at 4C overnight. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp2-90685_rabbit-monoclonal-ifn-gamma-r1-cd119-antibody-062-235202521451779.png)
![Western Blot: Serpin G1/C1 Inhibitor Antibody (18) [NBP2-89738] - Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:55 kDa Observed band size:71 kDa](http://images.novusbio.com/fullsize/Serpin-G1-C1-Inhibitor-Antibody-18-Western-Blot-NBP2-89738-img0002.jpg "Western Blot: Serpin G1/C1 Inhibitor Antibody (18) [NBP2-89738] - Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:55 kDa Observed band size:71 kDa")
![Immunoprecipitation: Serpin G1/C1 Inhibitor Antibody (18) [NBP2-89738] - Lane A:0.5 mg HepG2 Whole Cell Lysate 2 uL anti-SERPING1 rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody:Anti-SERPING1 rabbit monoclonal antibody,at 1:100 dilution Secondary antibody:Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution Developed using the odssey technique. Performed under reducing conditions.Predicted band size: 55 kDa Observed band size: 100 kDa](http://images.novusbio.com/fullsize/Serpin-G1-C1-Inhibitor-Antibody-18-Immunoprecipitation-NBP2-89738-img0001.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).](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)
![Flow Cytometry: HLA Class I Antibody (MEM-123) [NB500-505] - Surface staining of human peripheral blood with anti-HLA-class I (MEM-123) purified, GAM-APC.](http://images.novusbio.com/fullsize/HLA-Class-I-Antibody-MEM-123-Flow-Cytometry-NB500-505-img0002.jpg "Flow Cytometry: HLA Class I Antibody (MEM-123) [NB500-505] - Surface staining of human peripheral blood with anti-HLA-class I (MEM-123) purified, GAM-APC.")
![Flow Cytometry: HLA Class I Antibody (MEM-123) [NB500-505] - A surface stain was performed on human peripheral blood lymphocytes with HLA Class I (MEM-123) antibody NB500-505 (blue) and a matched isotype control (orange). Cells were incubated in an antibody dilution of 1 ug/mL for 20 minutes at room temperature, followed by mouse F(ab)2 IgG (H+L) APC-conjugated secondary antibody (F0101B, R&D Systems).](http://images.novusbio.com/fullsize/HLA-Class-I-Antibody-MEM-123-Flow-Cytometry-NB500-505-img0001.jpg)
![Western Blot: AIF-1/Iba1 Antibody (2A2-B6) [H00000199-M01] - Analysis of AIF1 expression in K-562 using AIF-1/Iba1 Antibody (2A2-B6).](http://images.novusbio.com/fullsize/AIF-1-Iba1-Antibody-2A2-B6-Western-Blot-H00000199-M01-img0005.jpg "Western Blot: AIF-1/Iba1 Antibody (2A2-B6) [H00000199-M01] - Analysis of AIF1 expression in K-562 using AIF-1/Iba1 Antibody (2A2-B6).")
![ELISA: AIF-1/Iba1 Antibody (2A2-B6) [H00000199-M01] - Detection limit for recombinant GST tagged AIF-1:Iba1 is 0.03 ng/ml using AIF-1:Iba1 Antibody (2A2-B6) as a capture antibody.](http://images.novusbio.com/fullsize/AIF-1-Iba1-Antibody-2A2-B6-ELISA-H00000199-M01-img0004.jpg)
![SDS-Page: Mouse IL-1ra/IL-1F3/IL1RN Protein [NBP2-35105]](http://images.novusbio.com/fullsize/Mouse-IL-1ra-IL-1F3-IL1RN-Protein-SDS-Page-NBP2-35105-img0001.jpg "SDS-Page: Mouse IL-1ra/IL-1F3/IL1RN Protein [NBP2-35105]")
![Flow Cytometry: L-Selectin/CD62L Antibody (DREG-56) - Chimeric [NBP2-81084] - Flow-cytometry using [NBP2-81084]. Human lymphocytes were stained with an isotype control (NBP2-52638, panel A) or the rabbit-chimeric version of DREG-56 (NBP2-81084, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/L-Selectin-CD62L-Antibody-DREG-56-Chimeric-Flow-Cytometry-NBP2-81084-img0001.jpg "Flow Cytometry: L-Selectin/CD62L Antibody (DREG-56) - Chimeric [NBP2-81084] - Flow-cytometry using [NBP2-81084]. Human lymphocytes were stained with an isotype control (NBP2-52638, panel A) or the rabbit-chimeric version of DREG-56 (NBP2-81084, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.")