| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-52534-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89830-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-87558-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26590-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-25266 | |||
| Azide and BSA Free | NBP2-25266SS | |||
![Western Blot: PLC-gamma 2 Antibody (3A8B6) [NBP2-52534] - Analysis using PLCG2 mouse mAb against A431 cell lysate.](http://images.novusbio.com/fullsize/PLC-gamma-2-Antibody-3A8B6-Western-Blot-NBP2-52534-img0005.jpg "Western Blot: PLC-gamma 2 Antibody (3A8B6) [NBP2-52534] - Analysis using PLCG2 mouse mAb against A431 cell lysate.")
![Immunocytochemistry/Immunofluorescence: PLC-gamma 2 Antibody (3A8B6) [NBP2-52534] - Immunofluorescence analysis of Hela cells using PLCG2 mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor- 555 phalloidin.](http://images.novusbio.com/fullsize/PLC-gamma-2-Antibody-3A8B6-Immunofluorescence-NBP2-52534-img0002.jpg)
![Flow Cytometry: PLC-gamma 2 Antibody (3A8B6) [NBP2-52534] - Analysis of Hela cells using PLCG2 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/PLC-gamma-2-Antibody-3A8B6-Flow-Cytometry-NBP2-52534-img0001.jpg)
![ELISA: PLC-gamma 2 Antibody (3A8B6) [NBP2-52534] - Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng).](http://images.novusbio.com/fullsize/PLC-gamma-2-Antibody-3A8B6-ELISA-NBP2-52534-img0004.jpg)
![Western Blot: CD39L4/ENTPD5 Antibody (064) [NBP2-89830] - Anti-CD39L4/ENTPD5 rabbit monoclonal antibody at 1:500 dilution. Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 µg per lane. Secondary: Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Performed under reducing conditions. Predicted band size: 47 kDa Observed band size: 53 kDa](http://images.novusbio.com/fullsize/CD39L4-ENTPD5-Antibody-064-Western-Blot-NBP2-89830-img0001.jpg "Western Blot: CD39L4/ENTPD5 Antibody (064) [NBP2-89830] - Anti-CD39L4/ENTPD5 rabbit monoclonal antibody at 1:500 dilution. Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 µg per lane. Secondary: Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Performed under reducing conditions. Predicted band size: 47 kDa Observed band size: 53 kDa")
![Immunohistochemistry-Paraffin: CD39L4/CD39L4/ENTPD5 Antibody (064) [NBP2-89830] - Immunochemical staining of human CD39L4/ENTPD5 in human liver with NBP2-89830 at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp2-89830_rabbit-monoclonal-cd39l4-entpd5-antibody-064-235202511545677.png)
![Immunohistochemistry-Paraffin: CD39L4/CD39L4/ENTPD5 Antibody (064) [NBP2-89830] - Immunochemical staining of human CD39L4/ENTPD5 in human kidney with NBP2-89830 at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp2-89830_rabbit-monoclonal-cd39l4-entpd5-antibody-064-235202511444489.png)
![Immunoprecipitation: CD39L4/ENTPD5 Antibody (064) [NBP2-89830] - ENTPD5 was immunoprecipitated using: Lane A:0.5 mg HepG2 Whole Cell Lysate 0.5 uL NBP2-89830 and 15 ul of 50 % Protein G agarose. Primary antibody: NBP2-89830 at 1:500 dilution. Secondary antibody: Clean-Bloto IP Detection Reagent (HRP) at 1:1000 dilution. Developed using the DAB staining technique. Performed under reducing conditions. Predicted band size: 47 kDa Observed band size: 47 kDa](http://images.novusbio.com/fullsize/nbp2-89830_rabbit-monoclonal-cd39l4-entpd5-antibody-064-23520251154565.png)
![Western Blot: Recombinant Human Tyrosine Hydroxylase His Protein [NBP1-42461] - Novus Biologicals antibody NB300-109 was used to detect the protein on a Western blot. 150 ng of protein were added to the Western blot.](http://images.novusbio.com/fullsize/Tyrosine-Hydroxylase-Protein-Western-Blot-NBP1-42461-img0002.jpg "Western Blot: Recombinant Human Tyrosine Hydroxylase His Protein [NBP1-42461] - Novus Biologicals antibody NB300-109 was used to detect the protein on a Western blot. 150 ng of protein were added to the Western blot.")
![SDS-Page: Recombinant Human Tyrosine Hydroxylase His Protein [NBP1-42461] - This product has a purity >95%. This protein was run on a 4-20% SDS-PAGE gel with 5 ug protein loaded.](http://images.novusbio.com/fullsize/Tyrosine-Hydroxylase-Protein-Immunoblotting-NBP1-42461-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: PLC-gamma 2 Antibody [NBP1-87558] - Immunofluorescent staining of human cell line U-251 MG shows localization to vesicles.](http://images.novusbio.com/fullsize/PLC-gamma-2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-87558-img0005.jpg "Immunocytochemistry/Immunofluorescence: PLC-gamma 2 Antibody [NBP1-87558] - Immunofluorescent staining of human cell line U-251 MG shows localization to vesicles.")
![Immunohistochemistry-Paraffin: PLC-gamma 2 Antibody [NBP1-87558] - Staining of human appendix shows strong cytoplasmic positivity in lymphoid tissue.](http://images.novusbio.com/fullsize/PLC-gamma-2-Antibody-Immunohistochemistry-Paraffin-NBP1-87558-img0002.jpg)
![Immunohistochemistry: FADS1 Antibody (7A10) [NBP3-26590] - Image of FADS1 Antibody (7A10) diluted at 1:100 and staining in paraffin-embedded human endometrial cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-262202414471574.jpg "Immunohistochemistry: FADS1 Antibody (7A10) [NBP3-26590] - Image of FADS1 Antibody (7A10) diluted at 1:100 and staining in paraffin-embedded human endometrial cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Western Blot: FADS1 Antibody (7A10) [NBP3-26590] - Positive Western Blot detected in: MCF-7 whole cell lysate, A549 whole cell lysate, Hela whole cell lysate. All lanes: FADS1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 52, 43 kDa Observed band size: 55 kDa](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-28220241152510.jpg)
![Immunocytochemistry/Immunofluorescence: FADS1 Antibody (7A10) [NBP3-26590] - Staining of HepG2 cell with FADS1 Antibody (7A10) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 565-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-282202412475112.jpg)
![Flow Cytometry: FADS1 Antibody (7A10) [NBP3-26590] - Overlay Peak curve showing HepG2 cells stained with FADS1 Antibody (7A10) (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-282202414183689.jpg)
![Western Blot: dUTPase Antibody [NB100-56624] - Detection of DUT-N in HeLa cell lysate using this antibody at a dilution of 1:1000.](http://images.novusbio.com/fullsize/dUTPase-Antibody-Western-Blot-NB100-56624-img0002.jpg "Western Blot: dUTPase Antibody [NB100-56624] - Detection of DUT-N in HeLa cell lysate using this antibody at a dilution of 1:1000.")
![Western Blot: Noxa Antibody (69N15C9) [NBP2-25251] - Western blot analysis of mouse A) Noxa recombinant protein, B) thymus and C) ovary using Noxa antibody at 1 ug/mL, 5 ug/mL and 5 ug/mL, respectively.](http://images.novusbio.com/fullsize/Noxa-Antibody-69N15C9-Western-Blot-NBP2-25251-img0001.jpg "Western Blot: Noxa Antibody (69N15C9) [NBP2-25251] - Western blot analysis of mouse A) Noxa recombinant protein, B) thymus and C) ovary using Noxa antibody at 1 ug/mL, 5 ug/mL and 5 ug/mL, respectively.")
![Immunohistochemistry-Paraffin: Cysteinyl Leukotriene R1/CysLTR1 Antibody [NBP1-85356] - Staining of human spleen shows strong cytoplasmic/membranous positivity in cells in red pulp.](http://images.novusbio.com/fullsize/Cysteinyl-Leukotriene-R1-CysLTR1-Antibody-Immunohistochemistry-Paraffin-NBP1-85356-img0010.jpg "Immunohistochemistry-Paraffin: Cysteinyl Leukotriene R1/CysLTR1 Antibody [NBP1-85356] - Staining of human spleen shows strong cytoplasmic/membranous positivity in cells in red pulp.")
![Immunohistochemistry-Paraffin: Cysteinyl Leukotriene R1/CysLTR1 Antibody [NBP1-85356] - Staining of human lung shows strong cytoplasmic positivity in macrophages.](http://images.novusbio.com/fullsize/Cysteinyl-Leukotriene-R1-CysLTR1-Antibody-Immunohistochemistry-Paraffin-NBP1-85356-img0006.jpg)
![Immunohistochemistry-Paraffin: Cysteinyl Leukotriene R1/CysLTR1 Antibody [NBP1-85356] - Staining of human endometrium shows no positivity in glandular cells, as expected.](http://images.novusbio.com/fullsize/Cysteinyl-Leukotriene-R1-CysLTR1-Antibody-Immunohistochemistry-Paraffin-NBP1-85356-img0007.jpg)
![Immunohistochemistry-Paraffin: Cysteinyl Leukotriene R1/CysLTR1 Antibody [NBP1-85356] - Staining of human liver shows no positivity in hepatocytes, as expected.](http://images.novusbio.com/fullsize/Cysteinyl-Leukotriene-R1-CysLTR1-Antibody-Immunohistochemistry-Paraffin-NBP1-85356-img0008.jpg)
![Immunohistochemistry-Paraffin: Cysteinyl Leukotriene R1/CysLTR1 Antibody [NBP1-85356] - Staining of human skin shows weak cytoplasmic/membranous positivity in squamous epithelial cells.](http://images.novusbio.com/fullsize/Cysteinyl-Leukotriene-R1-CysLTR1-Antibody-Immunohistochemistry-Paraffin-NBP1-85356-img0009.jpg)
![Western Blot: Muscle Phosphofructokinase/PFKM/PFK-1 Antibody [NBP2-32169] - Whole cell lysate HeLa, 293T, Jurkat, mouse TCMK-1, and mouse NIH3T3 cells.](http://images.novusbio.com/fullsize/Muscle-Phosphofructokinase-PFKM-PFK-1-Antibody-Western-Blot-NBP2-32169-img0004.jpg "<b>Biological Strategies Validation. </b>Western Blot: Muscle Phosphofructokinase/PFKM/PFK-1 Antibody [NBP2-32169] - Whole cell lysate HeLa, 293T, Jurkat, mouse TCMK-1, and mouse NIH3T3 cells.")
![<b>Biological Strategies Validation. </b>Immunoprecipitation: Muscle Phosphofructokinase/PFKM/PFK-1 Antibody [NBP2-32169] - Whole cell lysate 293T cells.](http://images.novusbio.com/fullsize/Muscle-Phosphofructokinase-PFKM-PFK-1-Antibody-Immunoprecipitation-NBP2-32169-img0003.jpg)
![Western Blot: Muscle Phosphofructokinase/PFKM/PFK-1 Antibody [NBP2-44228] - Analysis demonstrates the labeling specificity of the antibodies used for Tissue lysate from hog carotid arteries was analyzed by SDS-PAGE. Nitrocellulose membranes were probed with the corresponding antibodies at the same concentrations used for immunofluorescence labeling. 0.05 (PFK) and 0.2 mg (CAV-1) was loaded into lanes 1 and 2, respectively. Western blot development resulted in identification of the proteins of interest at the expected sizes, demonstrating the labeling specificity of the antibodies. Molecular weights are given. Used with permission from Vallejo and Hardin (2004).](http://images.novusbio.com/fullsize/Muscle-Phosphofructokinase-PFKM-PFK-1-Antibody-Western-Blot-NBP2-44228-img0003.jpg "Western Blot: Muscle Phosphofructokinase/PFKM/PFK-1 Antibody [NBP2-44228] - Analysis demonstrates the labeling specificity of the antibodies used for Tissue lysate from hog carotid arteries was analyzed by SDS-PAGE. Nitrocellulose membranes were probed with the corresponding antibodies at the same concentrations used for immunofluorescence labeling. 0.05 (PFK) and 0.2 mg (CAV-1) was loaded into lanes 1 and 2, respectively. Western blot development resulted in identification of the proteins of interest at the expected sizes, demonstrating the labeling specificity of the antibodies. Molecular weights are given. Used with permission from Vallejo and Hardin (2004).")
![Immunocytochemistry/Immunofluorescence: Muscle Phosphofructokinase/PFKM/PFK-1 Antibody [NBP2-44228] - Cultures of A7r5 VSM cells (rat aorta) were labeled with antibody and anti-caveolin (CAV)-1. Images from labeled A7r5 cells were acquired separately for PFK fluorescence (green) and CAV-1 fluorescence (red) from each cell. Used with permission from Vallejo and Hardin (2004).](http://images.novusbio.com/fullsize/Muscle-Phosphofructokinase-PFKM-PFK-1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-44228-img0001.jpg)
