| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89839-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89841-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89432-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89345-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99507-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89323-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-06087-50ul | |||
![Flow Cytometry: 15-PGDH/HPGD Antibody (016) [NBP2-89839] - Analysis of Human HPGD expression on Jurkat cells. The cells were treated , stained with purified anti-Human HPGD, 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/15-PGDH-HPGD-Antibody-016-Flow-Cytometry-NBP2-89839-img0002.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: 15-PGDH/HPGD Antibody (016) [NBP2-89839] - Analysis of Human HPGD expression on Jurkat cells. The cells were treated , stained with purified anti-Human HPGD, 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.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: 15-PGDH/HPGD Antibody (016) [NBP2-89839] - Staining of Human HPGD in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89839 antibody (1:60) 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.](http://images.novusbio.com/fullsize/nbp2-89839_rabbit-monoclonal-15-pgdh-hpgd-antibody-016-23520251628128.png)
![Flow Cytometry: 15-PGDH/HPGD Antibody (027) [NBP2-89841] - Analysis of Human HPGD expression on Jurkat cells. The cells were treated, stained with purified anti-Human HPGD, 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/15-PGDH-HPGD-Antibody-027-Flow-Cytometry-NBP2-89841-img0002.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: 15-PGDH/HPGD Antibody (027) [NBP2-89841] - Analysis of Human HPGD expression on Jurkat cells. The cells were treated, stained with purified anti-Human HPGD, 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.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: 15-PGDH/HPGD Antibody (027) [NBP2-89841] - Staining of Human HPGD in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89841 antibody (1:60) 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.](http://images.novusbio.com/fullsize/nbp2-89841_rabbit-monoclonal-15-pgdh-hpgd-antibody-027-23520252135140.png)
![Immunocytochemistry/Immunofluorescence: E-Selectin/CD62E Antibody (208) [NBP2-89432] - Staining of CD62E in TNF-a stimulated HUVEC cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-89432 antibody (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 cells membrane.](http://images.novusbio.com/fullsize/nbp2-89432_rabbit-monoclonal-e-selectin-cd62e-antibody-208-235202514371334.png "Immunocytochemistry/Immunofluorescence: E-Selectin/CD62E Antibody (208) [NBP2-89432] - Staining of CD62E in TNF-a stimulated HUVEC cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-89432 antibody (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 cells membrane.")
![Immunohistochemistry-Paraffin: Dicer Antibody [NBP3-30965] - Immunohistochemical staining of FFPE human colon carcinoma tissue using Dicer antibody (Cat. No. NBP3-30965). Antibody used at 1 ug/ml and visualized using DAB. Pathologists Comments: Cytoplasmic staining on mucous cells.](http://images.novusbio.com/fullsize/nbp3-30965_rabbit-dicer-pab-811202420592150.jpg "Immunohistochemistry-Paraffin: Dicer Antibody [NBP3-30965] - Immunohistochemical staining of FFPE human colon carcinoma tissue using Dicer antibody (Cat. No. NBP3-30965). Antibody used at 1 ug/ml and visualized using DAB. Pathologists Comments: Cytoplasmic staining on mucous cells.")
![Western Blot: c-Maf Antibody (JE39-57) [NBP3-32197] - Western blot analysis of c-Maf on different lysates with Rabbit anti-c-Maf antibody (NBP3-32197) at 1/1,000 dilution. Lane 1: A549 cell lysate (10 ug/Lane) Lane 2: Raji cell lysate (10 ug/Lane) Lane 3: Mouse lung tissue lysate (20 ug/Lane) Lane 4: Mouse kidney tissue lysate (20 ug/Lane) Lane 5: Rat spleen tissue lysate (20 ug/Lane) Lane 6: Rat kidney tissue lysate (20 ug/Lane) Predicted band size: 38 kDa Observed band size: 38 kDa Exposure time: 40 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 (NBP3-32197) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32197_rabbit-c-maf-mab-je39-57-278202416285292.jpg "Western Blot: c-Maf Antibody (JE39-57) [NBP3-32197] - Western blot analysis of c-Maf on different lysates with Rabbit anti-c-Maf antibody (NBP3-32197) at 1/1,000 dilution. Lane 1: A549 cell lysate (10 ug/Lane) Lane 2: Raji cell lysate (10 ug/Lane) Lane 3: Mouse lung tissue lysate (20 ug/Lane) Lane 4: Mouse kidney tissue lysate (20 ug/Lane) Lane 5: Rat spleen tissue lysate (20 ug/Lane) Lane 6: Rat kidney tissue lysate (20 ug/Lane) Predicted band size: 38 kDa Observed band size: 38 kDa Exposure time: 40 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 (NBP3-32197) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: COL4A3BP Antibody [NBP3-30940] - Immunohistochemical staining of normal human liver tissue using CERT antibody (Cat. No. NBP3-30940) at 15 ug/ml](http://images.novusbio.com/fullsize/nbp3-30940_rabbit-col4a3bp-pab-811202420592155.jpg "Immunohistochemistry: COL4A3BP Antibody [NBP3-30940] - Immunohistochemical staining of normal human liver tissue using CERT antibody (Cat. No. NBP3-30940) at 15 ug/ml")
![Western Blot: HLA Class I Antibody (MEM-147) [NB500-411] - Human Ramos B cell line lysate (1% laurylmaltoside); non-reduced sample, immunostained by mAb MEM-147 and goat anti-mouse IgG (H+L)-HRP conjugate.](http://images.novusbio.com/fullsize/HLA-Class-I-Antibody-MEM-147-Western-Blot-NB500-411-img0002.jpg "Western Blot: HLA Class I Antibody (MEM-147) [NB500-411] - Human Ramos B cell line lysate (1% laurylmaltoside); non-reduced sample, immunostained by mAb MEM-147 and goat anti-mouse IgG (H+L)-HRP conjugate.")
![Flow Cytometry: Leptin/OB Antibody (002) [NBP2-89345] - Analysis of Human LEP expression on HeLa cells. The cells were treated, stained with purified anti-Human LEP, 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/Leptin-OB-Antibody-002-Flow-Cytometry-NBP2-89345-img0001.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: Leptin/OB Antibody (002) [NBP2-89345] - Analysis of Human LEP expression on HeLa cells. The cells were treated, stained with purified anti-Human LEP, 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.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Leptin/OB Antibody (002) [NBP2-89345] - Staining of LEP in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP2-89345 (dilution ratio 1:60) at 4c overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG secondary antibody (red). Positive staining was localized to Cytoplasm .](http://images.novusbio.com/fullsize/nbp2-89345_rabbit-monoclonal-leptin-ob-antibody-002-23520251129371.png)
![Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (EOS9.1) - Low Endotoxin, Azide and BSA Free [NBP3-09092] - Separation of anti-CD95 (EOS9.1) antibody stimulated CEM cells (24 hours, 1 ug/ml, red-filled) from nonstimulated CEM cells (black-dashed) in flow cytometry analysis CEM cell suspension stained using ApoFlowEx kit (ED7044).](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-EOS9-1-Low-Endotoxin-Azide-and-BSA-Free-Flow-Cytometry-NBP3-09092-img0002.jpg "Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (EOS9.1) - Low Endotoxin, Azide and BSA Free [NBP3-09092] - Separation of anti-CD95 (EOS9.1) antibody stimulated CEM cells (24 hours, 1 ug/ml, red-filled) from nonstimulated CEM cells (black-dashed) in flow cytometry analysis CEM cell suspension stained using ApoFlowEx kit (ED7044).")
![Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (EOS9.1) - Low Endotoxin, Azide and BSA Free [NBP3-09092] - Separation of anti-CD95 (EOS9.1) antibody stimulated Jurkat cells (24 hours, 4 ug/ml, red-filled) from nonstimulated Jurkat cells (black-dashed) in flow cytometry analysis of Jurkat cellular suspension stained using ApoFlowEx kit (ED7044).](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-EOS9-1-Low-Endotoxin-Azide-and-BSA-Free-Flow-Cytometry-NBP3-09092-img0001.jpg)
![Western Blot: CD97 Antibody [NBP2-99507] - Anti-CD97 rabbit polyclonal antibody at 1:500 dilution. Lane A: NIH/3T3 Whole Cell Lysate. Lane B: HepG2 Whole Cell Lysate. Lane C: Raw264.7 Whole Cell Lysate. Lane D: Mouse spleen tissue lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 92 kDa](http://images.novusbio.com/fullsize/CD97-Antibody-Western-Blot-NBP2-99507-img0002.jpg "Western Blot: CD97 Antibody [NBP2-99507] - Anti-CD97 rabbit polyclonal antibody at 1:500 dilution. Lane A: NIH/3T3 Whole Cell Lysate. Lane B: HepG2 Whole Cell Lysate. Lane C: Raw264.7 Whole Cell Lysate. Lane D: Mouse spleen tissue lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 92 kDa")
![Immunoprecipitation: CD97 Antibody [NBP2-99507] - CD97 was immunoprecipitated using: Lane A: 0.5 mg NIH/3T3 Whole Cell Lysate. 4 ul anti-CD97 rabbit polyclonal antibody and 60 ug of Immunomagnetic beads. Protein A/G. Primary antibody: Anti-CD97 rabbit polyclonal antibody, at 1:100 dilution. Secondary antibody: Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 92 kDa. Observed band size: 70 kDa](http://images.novusbio.com/fullsize/CD97-Antibody-Immunoprecipitation-NBP2-99507-img0003.jpg)
![Western Blot: Glutathione S-Transferase pi 1/GSTP1 Antibody (003) [NBP2-89323] - Lane A: Jurkat Whole Cell Lysate Lane B: K562 Whole Cell LysateLane C: HeLa Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique. Performed under reducing conditions.Predicted band size:23 kDa](http://images.novusbio.com/fullsize/Glutathione-S-Transferase-pi-1-GSTP1-Antibody-003-Western-Blot-NBP2-89323-img0001.jpg "Western Blot: Glutathione S-Transferase pi 1/GSTP1 Antibody (003) [NBP2-89323] - Lane A: Jurkat Whole Cell Lysate Lane B: K562 Whole Cell LysateLane C: HeLa Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique. Performed under reducing conditions.Predicted band size:23 kDa")
![<b>Genetic Strategies Validation. </b>NBP2-89323 used at 1:500 dilution. Lane A: Hela Whole Cell Lysate. Lane B: GSTP1 knockout Hela Whole Cell Lysate. Lysates loaded at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)[HRP] used at at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 23 kDa.](http://images.novusbio.com/fullsize/nbp2-89323_rabbit-monoclonal-esam-antibody-202-45202316595485.png)
![Western Blot: Latexin Antibody (8E1G6C1D4) [NBP3-06087] - Anti-LXN mouse monoclonal antibody at 1:500 dilution Lane A: A549 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary: Goat Anti-Mouse IgG H&L (Dylight800) at 115000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:26 kDa Observed band size:26 kDa](http://images.novusbio.com/fullsize/Latexin-Antibody-8E1G6C1D4-Western-Blot-NBP3-06087-img0001.jpg "Western Blot: Latexin Antibody (8E1G6C1D4) [NBP3-06087] - Anti-LXN mouse monoclonal antibody at 1:500 dilution Lane A: A549 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary: Goat Anti-Mouse IgG H&L (Dylight800) at 115000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:26 kDa Observed band size:26 kDa")
![Immunoprecipitation: Latexin Antibody (8E1G6C1D4) [NBP3-06087] - LXN was immunoprecipitated using: Lane A: 0.5 mg MCF-7 Whole Cell Lysate 0.5 uL anti-LXN mouse monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-LXN mouse monoclonal antibody, at 1:500 dilution Secondary antibody: Dylight 800-labeled antibody to Mouse IgG (H+L), at 1:7500 dilution Developed using the odssey technique.Performed under reducing conditions.Predicted band size: 25.7 kDa Observed band size: 27 kDa](http://images.novusbio.com/fullsize/Latexin-Antibody-8E1G6C1D4-Immunoprecipitation-NBP3-06087-img0002.jpg)