| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89621-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-37713 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48113 | |||
| Azide and BSA Free | NBP2-34756-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-35333SS | |||
| Azide and BSA Free | NBP2-80622 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-2181SS | |||
| Azide and BSA Free | NBP2-80646 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-44853 | |||
| Azide and BSA Free | NBP2-34527-0.1mg | |||
![Western Blot: JNK2 Antibody (011) [NBP2-89621] - Lane A: Jurkat 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:48 kDa Observed band size:54 kDa (We are unsure as to the identity of these extra bands.)](http://images.novusbio.com/fullsize/JNK2-Antibody-011-Western-Blot-NBP2-89621-img0004.jpg "Western Blot: JNK2 Antibody (011) [NBP2-89621] - Lane A: Jurkat 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:48 kDa Observed band size:54 kDa (We are unsure as to the identity of these extra bands.)")
![Immunocytochemistry/Immunofluorescence: JNK2 Antibody (011) [NBP2-89621] - Staining of Human MAPK9 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with Rabbit anti-Human MAPK9 monoclonal antibody (1:300) at 37c 1 hour. 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 Nucleus.](http://images.novusbio.com/fullsize/JNK2-Antibody-011-Immunocytochemistry-Immunofluorescence-NBP2-89621-img0001.jpg)
![Immunohistochemistry-Paraffin: JNK2 Antibody (011) [NBP2-89621] - Staining of human MAPK9 in human brain with rabbit mnoclonal antibody (1:1000).](http://images.novusbio.com/fullsize/JNK2-Antibody-011-Immunohistochemistry-Paraffin-NBP2-89621-img0003.jpg)
![Immunohistochemistry-Paraffin: JNK2 Antibody (011) [NBP2-89621] - Staining of human MAPK9 in human kidney with rabbit monoclonal antibody (1:1000).](http://images.novusbio.com/fullsize/JNK2-Antibody-011-Immunohistochemistry-Paraffin-NBP2-89621-img0002.jpg)
![Immunoprecipitation: JNK2 Antibody (011) [NBP2-89621] - Lane A:0.5 mg HepG2 Whole Cell Lysate Lane B:0.5 mg Hela Whole Cell LysateLane C:0.5 mg Jurkat Whole Cell Lysate Lane D:0.5 mg MCF-7 Whole Cell Lysate0.5 uL anti-MAPK9 rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-MAPK9 rabbit monoclonal antibody,at 1:500 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: 44 kDa Observed band size: 44 kDa](http://images.novusbio.com/fullsize/JNK2-Antibody-011-Immunoprecipitation-NBP2-89621-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: JNK2 Antibody (011) [NBP2-89621] - Staining of Human MAPK9 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89621 antibody (1:300) at 37c 1 hour. 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 Nucleus.](http://images.novusbio.com/fullsize/nbp2-89621_rabbit-monoclonal-jnk2-antibody-011-23520251544322.png)
![Flow Cytometry: Fc gamma RIII (CD16) Antibody (MEM-154) [NB500-378] - Separation of FasL transfected L5178Y cells stained using anti-human CD178 (NOK-1) purified antibody (concentration in sample 9 ug/ml, GAM APC, red-filled) from FasL transfected L5178Y cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (surface staining).](http://images.novusbio.com/fullsize/Fc-gamma-RIII-CD16-Antibody-MEM-154-Flow-Cytometry-NB500-378-img0002.jpg "Flow Cytometry: Fc gamma RIII (CD16) Antibody (MEM-154) [NB500-378] - Separation of FasL transfected L5178Y cells stained using anti-human CD178 (NOK-1) purified antibody (concentration in sample 9 ug/ml, GAM APC, red-filled) from FasL transfected L5178Y cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (surface staining).")
![Flow Cytometry: Fc gamma RIII (CD16) Antibody (MEM-154) [NB500-378] - Flow cytometry surface staining pattern of human peripheral blood stained using Fc gamma RIII (CD16) Antibody (MEM-154) purified antibody (concentration in sample 2 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/Fc-gamma-RIII-CD16-Antibody-MEM-154-Flow-Cytometry-NB500-378-img0001.jpg)
![Flow Cytometry: Fc gamma RIII (CD16) Antibody (MEM-154) - BSA Free [NB500-378] - Staining of human peripheral blood cells with anti-human CD16 (MEM-154) purified, GAM/APC.](http://images.novusbio.com/fullsize/nb500-378_mouse-monoclonal-fc-gamma-riii-cd16-antibody-mem-154-17720241003218.jpg)
![Flow Cytometry: Siglec-1/CD169 Antibody (7-239) [NBP2-37729] - Staining of CD169 on buffy coat diff. monocytes by anti-CD169 (7-239) PE.](http://images.novusbio.com/fullsize/Siglec-1-CD169-Antibody-7-239-Flow-Cytometry-NBP2-37729-img0001.jpg "Flow Cytometry: Siglec-1/CD169 Antibody (7-239) [NBP2-37729] - Staining of CD169 on buffy coat diff. monocytes by anti-CD169 (7-239) PE.")
![Flow Cytometry: Fc gamma RIIIA/CD16a Antibody (MEM-168) [NB500-523] - Analysis using the Alexa Fluor (R) 647 conjugate of NB500-523. Staining of CD16a in human buffy coat using anti-CD16a antibody. The primary antibody was used at a dilution of 1:100 and incubated for 25 min at 4C in 2% human serum, 0.5 mM EDTA in DPBS. Ima](http://images.novusbio.com/fullsize/Fc-gamma-RIIIA-CD16a-Antibody-MEM-168-Flow-Cytometry-NB500-523-img0005.jpg "Flow Cytometry: Fc gamma RIIIA/CD16a Antibody (MEM-168) [NB500-523] - Analysis using the Alexa Fluor (R) 647 conjugate of NB500-523. Staining of CD16a in human buffy coat using anti-CD16a antibody. The primary antibody was used at a dilution of 1:100 and incubated for 25 min at 4C in 2% human serum, 0.5 mM EDTA in DPBS. Ima")
![Flow Cytometry: Fc gamma RIIIA/CD16a Antibody (MEM-168) [NB500-523] - Surface staining of lysed and washed porcine peripheral blood with purified anti-CD16 (MEM-168) (detection by anti-mouse IgM FITC). Panel A - porcine PBMC stained with Isotype mouse IgM control (PFR-03) Panel B, C, D - three different porcine PMBC samples stained with anti-CD16 (MEM-168) Cells in the granulocyte gate were used for analysis.](http://images.novusbio.com/fullsize/Fc-gamma-RIIIA-CD16a-Antibody-MEM-168-Flow-Cytometry-NB500-523-img0001.jpg)
![Flow Cytometry: Fc gamma RIIIA/CD16a Antibody (MEM-168) [NB500-523] - Analysis using the Alexa Fluor (R) 488 conjugate of NB500-523. Staining of CD16a in human buffy coat using anti-CD16a antibody AF488. The primary antibody was used at a dilution of 1:100 and incubated for 25 min at 4C in 2% human serum, 0.5 mM EDTA in DPBS. Image from verified customer review.](http://images.novusbio.com/fullsize/Fc-gamma-RIIIA-CD16a-Antibody-MEM-168-Flow-Cytometry-NB500-523-img0004.jpg)
![Flow Cytometry: Fc gamma RIIIA/CD16a Antibody (MEM-168) [NB500-523] - Human PBMC stained with Fc gamma RIIIA/CD16a antibody. Image from verified customer review.](http://images.novusbio.com/fullsize/Fc-gamma-RIIIA-CD16a-Antibody-MEM-168-Flow-Cytometry-NB500-523-img0007.jpg)
![Western Blot: CXCR5 Antibody (JB11-40) [NBP2-75460] - Western blot analysis of CXCR5 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Daudi cell lysate Lane 2: Raji cell lysate](http://images.novusbio.com/fullsize/CXCR5-Antibody-JB11-40-Western-Blot-NBP2-75460-img0006.jpg "Western Blot: CXCR5 Antibody (JB11-40) [NBP2-75460] - Western blot analysis of CXCR5 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Daudi cell lysate Lane 2: Raji cell lysate")
![Immunohistochemistry-Paraffin: CXCR5 Antibody (JB11-40) [NBP2-75460] - Analysis of paraffin-embedded rat kidney tissue using anti-CXCR5 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CXCR5-Antibody-JB11-40-Immunohistochemistry-Paraffin-NBP2-75460-img0004.jpg)
![Flow Cytometry: CXCR5 Antibody (JB11-40) [NBP2-75460] - Analysis of Daudi cells with CXCR5 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody.](http://images.novusbio.com/fullsize/CXCR5-Antibody-JB11-40-Flow-Cytometry-NBP2-75460-img0001.jpg)
![Immunohistochemistry-Paraffin: CXCR5 Antibody (JB11-40) [NBP2-75460] - Analysis of paraffin-embedded human tonsil tissue using anti-CXCR5 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CXCR5-Antibody-JB11-40-Immunohistochemistry-Paraffin-NBP2-75460-img0002.jpg)
![Immunohistochemistry-Paraffin: CXCR5 Antibody (JB11-40) [NBP2-75460] - Analysis of paraffin-embedded mouse heart tissue using anti-CXCR5 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CXCR5-Antibody-JB11-40-Immunohistochemistry-Paraffin-NBP2-75460-img0003.jpg)
![Western Blot: HLA DRB1 Antibody (SPM289) [NBP2-45311] - Western Blot Analysis of Ramos cells and human spleen tissue lysate using HLA DRB1 Antibody (SPM289).](http://images.novusbio.com/fullsize/HLA-DRB1-Antibody-SPM289-Western-Blot-NBP2-45311-img0004.jpg "Western Blot: HLA DRB1 Antibody (SPM289) [NBP2-45311] - Western Blot Analysis of Ramos cells and human spleen tissue lysate using HLA DRB1 Antibody (SPM289).")
![Immunohistochemistry-Paraffin: HLA DRB1 Antibody (SPM289) [NBP2-45311] - Human Tonsil stained with HLA-DRB Monoclonal Antibody (SPM289).](http://images.novusbio.com/fullsize/HLA-DRB1-Antibody-SPM289-Immunohistochemistry-Paraffin-NBP2-45311-img0001.jpg)
![Flow Cytometry: HLA DRB1 Antibody (SPM289) [NBP2-45311] - Flow Cytometric Analysis of human Raji cells using HLA DRB1 Antibody (SPM289).followed by Goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/HLA-DRB1-Antibody-SPM289-Flow-Cytometry-NBP2-45311-img0002.jpg)
![Immunofluorescence: HLA DRB1 Antibody (SPM289) [NBP2-45311] - ICC/IF analysis of Raji cells labeling HLA-DR with conjugated with APC (Green) The nuclear counterstain is Red Dot (Red)](http://images.novusbio.com/fullsize/HLA-DRB1-Antibody-SPM289-Immunofluorescence-NBP2-45311-img0003.jpg)
![Western Blot: CCR2 Antibody (2D8) [NBP2-35333] - Analysis of CCR2 [2D8] in Molt4 lysate](http://images.novusbio.com/fullsize/CCR2-Antibody-2D8-Western-Blot-NBP2-35333-img0003.jpg "Western Blot: CCR2 Antibody (2D8) [NBP2-35333] - Analysis of CCR2 [2D8] in Molt4 lysate")
![Immunohistochemistry-Paraffin: CCR2 Antibody (2D8) [NBP2-35333] - Analysis of FFPE tissue section of human esophageal squamous cell carcinoma (SCC) using CCR2 antibody (clone 2D8) at 5 ug/ml concentration. The cancer cells depicted strong cytoplasmic-membranous immunostaining, whereas the cells of tumor stroma were largely negative for CCR2 immunopositivity.](http://images.novusbio.com/fullsize/CCR2-Antibody-2D8-Immunohistochemistry-Paraffin-NBP2-35333-img0002.jpg)
![Immunohistochemistry-Paraffin: CCR2 Antibody (2D8) [NBP2-35333] - Analysis of FFPE tissue section of human breast using CCR2 antibody (clone 2D8) at 5 ug/ml concentration. The glandular cells in the lobules showed a specific cytoplasmic-membranous immunostaining, whereas, the inter-lobular connective tissue did not develop any staining for CCR2.](http://images.novusbio.com/fullsize/CCR2-Antibody-2D8-Immunohistochemistry-Paraffin-NBP2-35333-img0001.jpg)
![Flow Cytometry: CD4 Antibody (B486A1) [NB100-2181] - Analysis of blood T cells using CD4 mouse mAb (M2) and negative control (M1).](http://images.novusbio.com/fullsize/CD4-Antibody-B486A1-Flow-Cytometry-NB100-2181-img0004.jpg "Flow Cytometry: CD4 Antibody (B486A1) [NB100-2181] - Analysis of blood T cells using CD4 mouse mAb (M2) and negative control (M1).")
![Western Blot: CD4 Antibody (B486A1) [NB100-2181] - Analysis of human tonsil tissue using CD4 antibody at a concentration of 2 ug/ml.](http://images.novusbio.com/fullsize/CD4-Antibody-B486A1-Western-Blot-NB100-2181-img0005.jpg)
![Formalin-fixed, paraffin-embedded human tonsil stained with CD45 antibody (2B11) [NBP2-32934].](http://images.novusbio.com/fullsize/CD45-Antibody-2B11-Immunohistochemistry-Paraffin-NBP2-32934-img0002.jpg "Formalin-fixed, paraffin-embedded human tonsil stained with CD45 antibody (2B11) [NBP2-32934].")
![Formalin-fixed, paraffin-embedded human tonsil (10X) stained with CD45 antibody (2B11) [NBP2-32934].](http://images.novusbio.com/fullsize/CD45-Antibody-2B11-Immunohistochemistry-Paraffin-NBP2-32934-img0001.jpg)
![Immunohistochemistry-Paraffin: FCER1G Antibody [NBP2-16456] - Immunohistochemical analysis of paraffin-embedded U873 xenograft, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/FCER1G-Antibody-Immunohistochemistry-Paraffin-NBP2-16456-img0002.jpg "Immunohistochemistry-Paraffin: FCER1G Antibody [NBP2-16456] - Immunohistochemical analysis of paraffin-embedded U873 xenograft, using antibody at 1:100 dilution.")
![ICC/IF-FCER1G Antibody [NBP2-16456] -HepG2 cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: FCER1G stained by FCER1G antibody [N2C3] diluted at 1:500. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [114] diluted at 1:1000.Blue: Fluoroshield with DAPI. Scale bar= 10um.](http://images.novusbio.com/fullsize/antibody/nbp2-16456_rabbit-polyclonal-fcer1g-antibody-immunocytochemistry-immunofluorescence-2572023123444..jpg)
![Western Blot: FCER1G Antibody [NBP2-16456] - Various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with FCER1G antibody [N2C3] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/antibody/nbp2-16456_rabbit-polyclonal-fcer1g-antibody-western-blot-2572023123637..jpg)
![Western Blot: FCER1G Antibody [NBP2-16456] - Non-transfected - and transfected (+) 293T whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with FCER1G antibody [N2C3]diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/antibody/nbp2-16456_rabbit-polyclonal-fcer1g-antibody-western-blot-2572023123822..jpg)
![FCER1G Antibody [NBP2-16456] - THP-1 cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: FCER1G stained by FCER1G antibody [N2C3] diluted at 1:500.Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/antibody/nbp2-16456_rabbit-polyclonal-fcer1g-antibody-immunocytochemistry-immunofluorescence-257202312404..jpg)
![<b>Orthogonal Strategies Validation. </b>Western Blot: FCER1G Antibody [NBP2-16456] - Various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with FCER1G antibody [N2C3] diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.](http://images.novusbio.com/fullsize/nbp2-16456_rabbit-polyclonal-fcer1g-antibody-1610202419414525.jpg)
![Western Blot: gp130/CD130 Antibody [NBP2-15776] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with CD130 antibody diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/gp130-CD130-Antibody-Western-Blot-NBP2-15776-img0009.jpg "Western Blot: gp130/CD130 Antibody [NBP2-15776] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with CD130 antibody diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: gp130/CD130 Antibody [NBP2-15776] - Human breast carcinoma. CD130 stained by CD130 antibody diluted at 1:7500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/gp130-CD130-Antibody-Immunohistochemistry-Paraffin-NBP2-15776-img0010.jpg)
![Immunohistochemistry-Paraffin: gp130/CD130 Antibody [NBP2-15776] - J5 xenograft, using CD130 antibody at 1:500 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/gp130-CD130-Antibody-Immunohistochemistry-Paraffin-NBP2-15776-img0004.jpg)