| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-03787-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-03814-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-35774-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-29664-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81067-0.025mg | |||
![Western Blot: Hyaluronan synthase 2 Antibody [NBP3-03787] - Analysis of various lysates, using HAS2 antibody at 1:500 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. xposure time: 180s.](http://images.novusbio.com/fullsize/antibody/nbp3-03787_rabbit-polyclonal-hyaluronan-synthase-2-antibody-western-blot-206202313155..jpg "Western Blot: Hyaluronan synthase 2 Antibody [NBP3-03787] - Analysis of various lysates, using HAS2 antibody at 1:500 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. xposure time: 180s.")
![Western Blot: Hyaluronan synthase 1 Antibody [NBP3-03814] - Analysis of extracts of various cell lines, using Hyaluronan synthase 1 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.](http://images.novusbio.com/fullsize/Hyaluronan-synthase-1-Antibody-Western-Blot-NBP3-03814-img0001.jpg "Western Blot: Hyaluronan synthase 1 Antibody [NBP3-03814] - Analysis of extracts of various cell lines, using Hyaluronan synthase 1 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.")
![Western Blot: Hey L Antibody [NBP3-35774] - Western blot analysis of various lysates, using Hey L Rabbit pAb at 1:2500 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 30s.](http://images.novusbio.com/fullsize/nbp3-35774_rabbit-hey-l-pab-1012202411433429.jpg "Western Blot: Hey L Antibody [NBP3-35774] - Western blot analysis of various lysates, using Hey L Rabbit pAb at 1:2500 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 30s.")
![Western Blot: Doublecortin Antibody (6H1B3) [NBP3-15628] - Western blot analysis of extracts of various cell lines, using Doublecortin antibody (NBP3-15628) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.](http://images.novusbio.com/fullsize/Doublecortin-Antibody-6H1B3-Western-Blot-NBP3-15628-img0001.jpg "Western Blot: Doublecortin Antibody (6H1B3) [NBP3-15628] - Western blot analysis of extracts of various cell lines, using Doublecortin antibody (NBP3-15628) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.")
![Western Blot: OLIG2 [p Ser14, p Ser10, p Ser13] Antibody [NBP2-29523] - Western blot of rat neonatal brain lysate showing specific immunolabeling of the ~ 32k form of the Olig2 protein phosphorylated at Ser10,13,14. Immunolabeling is blocked by the phospho-peptide used as antigen (peptide), but not by the corresponding dephospho-peptide (not shown).](http://images.novusbio.com/fullsize/OLIG2-[p-Ser14-p-Ser10-p-Ser13]-Antibody-Western-Blot-NBP2-29523-img0001.jpg "Western Blot: OLIG2 [p Ser14, p Ser10, p Ser13] Antibody [NBP2-29523] - Western blot of rat neonatal brain lysate showing specific immunolabeling of the ~ 32k form of the Olig2 protein phosphorylated at Ser10,13,14. Immunolabeling is blocked by the phospho-peptide used as antigen (peptide), but not by the corresponding dephospho-peptide (not shown).")
![Western Blot: Tryptophan Hydroxylase 1 [p Ser260] Antibody [NB300-307] - Rat brainstem lysate showing specific immunolabeling of the ~55k TPH phosphorylated at Ser260. The labeling by Anti-Ser260TPH is specifically blocked by the Ser260 phosphopeptide (Phos-pep) used as antigen. The corresponding nonphosphopeptide (Nonphos-pep) did not block the immunolabeling.](http://images.novusbio.com/fullsize/Tryptophan-Hydroxylase-1-[p-Ser260]-Antibody-Western-Blot-NB300-307-img0001.jpg "Western Blot: Tryptophan Hydroxylase 1 [p Ser260] Antibody [NB300-307] - Rat brainstem lysate showing specific immunolabeling of the ~55k TPH phosphorylated at Ser260. The labeling by Anti-Ser260TPH is specifically blocked by the Ser260 phosphopeptide (Phos-pep) used as antigen. The corresponding nonphosphopeptide (Nonphos-pep) did not block the immunolabeling.")
![Western Blot: Tryptophan Hydroxylase 1 [p Ser58] Antibody [NB300-260] - Recombinant tryptophan hydroxylase incubated in the absence (Control) and presence of cAMP-dependent protein kinase (PKA) showing specific immunolabeling of the ~53k tryptophan hydroxylase protein phosphorylated at Ser58.](http://images.novusbio.com/fullsize/Tryptophan-Hydroxylase-1-[p-Ser58]-Antibody-Western-Blot-NB300-260-img0002.jpg "Western Blot: Tryptophan Hydroxylase 1 [p Ser58] Antibody [NB300-260] - Recombinant tryptophan hydroxylase incubated in the absence (Control) and presence of cAMP-dependent protein kinase (PKA) showing specific immunolabeling of the ~53k tryptophan hydroxylase protein phosphorylated at Ser58.")
![Western Blot: GAP43 [p Ser41] Antibody [NB300-179] - Western blot of rat cortex lysate showing specific immunolabeling of the ~50k Gap-43 protein phosphorylated at Ser41 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase). The blot is identical to the control except that it was incubated in lambda-phosphatase (1200 units for 30 min) before being exposed to the GAP-43 Ser41 antibody. The immunolabeling of GAP-43 is completely eliminated by treatment with lambda-phosphatase.](http://images.novusbio.com/fullsize/GAP43-[p-Ser41]-Antibody-Western-Blot-NB300-179-img0002.jpg "Western Blot: GAP43 [p Ser41] Antibody [NB300-179] - Western blot of rat cortex lysate showing specific immunolabeling of the ~50k Gap-43 protein phosphorylated at Ser41 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase). The blot is identical to the control except that it was incubated in lambda-phosphatase (1200 units for 30 min) before being exposed to the GAP-43 Ser41 antibody. The immunolabeling of GAP-43 is completely eliminated by treatment with lambda-phosphatase.")
![Western Blot: eNOS [p Ser116] Antibody [NBP2-29664] - Untreated (lane 1) and lambda phosphatase-treated (lane 2) Fetal bovine heart endothelial cell lysate was probed with anti-phospho-eNOS (1:1000).](http://images.novusbio.com/fullsize/eNOS-[p-Ser116]-Antibody-Western-Blot-NBP2-29664-img0002.jpg "Western Blot: eNOS [p Ser116] Antibody [NBP2-29664] - Untreated (lane 1) and lambda phosphatase-treated (lane 2) Fetal bovine heart endothelial cell lysate was probed with anti-phospho-eNOS (1:1000).")
![Western Blot: Ceruloplasmin Antibody (JE59-01) [NBP3-32182] - Western blot analysis of Ceruloplasmin on different lysates with Rabbit anti-Ceruloplasmin antibody (NBP3-32182) at 1/1,000 dilution. Lane 1: Rat liver tissue lysate Lane 2: Rat testis tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 122 kDa Observed band size: 140 kDa Exposure time: 3 minutes 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 (NBP3-32182) 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/nbp3-32182_rabbit-ceruloplasmin-mab-je59-01-278202415212439.jpg "Western Blot: Ceruloplasmin Antibody (JE59-01) [NBP3-32182] - Western blot analysis of Ceruloplasmin on different lysates with Rabbit anti-Ceruloplasmin antibody (NBP3-32182) at 1/1,000 dilution. Lane 1: Rat liver tissue lysate Lane 2: Rat testis tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 122 kDa Observed band size: 140 kDa Exposure time: 3 minutes 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 (NBP3-32182) 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: Ki67/MKI67 Antibody (PD00-10) [NBP3-32453] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Mouse anti-Ki67/MKI67 antibody (NBP3-32453) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (NBP3-32453) 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/nbp3-32453_mouse-ki67-mki67-mab-pd00-10-298202414333629.jpg "Immunohistochemistry: Ki67/MKI67 Antibody (PD00-10) [NBP3-32453] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Mouse anti-Ki67/MKI67 antibody (NBP3-32453) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (NBP3-32453) 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.")