| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-62753-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50285-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-97504-0.2mg | |||
| BSA Free | NBP1-97504-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-1543-0.025ml | |||
![Western Blot: Syntaxin-BP1 [p Ser515] Antibody [NB300-742] - Rat cortex lysate showing specific immunolabeling of the ~65k Munc-18 protein phosphorylated at Ser513. Immunolabeling is blocked by the phosphopeptide (peptide) used as antigen but not by the corresponding dephosphopeptide (not shown).](http://images.novusbio.com/fullsize/Syntaxin-BP1-[p-Ser515]-Antibody-Western-Blot-NB300-742-img0001.jpg "Western Blot: Syntaxin-BP1 [p Ser515] Antibody [NB300-742] - Rat cortex lysate showing specific immunolabeling of the ~65k Munc-18 protein phosphorylated at Ser513. Immunolabeling is blocked by the phosphopeptide (peptide) used as antigen but not by the corresponding dephosphopeptide (not shown).")
![Immunohistochemistry: Syntaxin-BP1 [p Ser513] Antibody [NB300-742] - Immunostaining of 14 DIV rat cortical neurons showing specific labeling of Munc-18 phosphorylated at Ser513 (red) and PSD95 (green). Photo courtesy of Gang Liu.](http://images.novusbio.com/fullsize/Syntaxin-BP1-[p-Ser513]-Antibody-Immunohistochemistry-NB300-742-img0004.jpg)
![Western Blot: Aquaporin-2 [p Ser269] Antibody [NBP1-48314] - vasopressin (AVP) treated rat kidney lysate showing specific immunolabeling of the approx 29k and 37k glycosylated form of the AQP2 protein phosphorylated at Ser269.](http://images.novusbio.com/fullsize/Aquaporin-2-[p-Ser269]-Antibody-Western-Blot-NBP1-48314-img0001.jpg "Western Blot: Aquaporin-2 [p Ser269] Antibody [NBP1-48314] - vasopressin (AVP) treated rat kidney lysate showing specific immunolabeling of the approx 29k and 37k glycosylated form of the AQP2 protein phosphorylated at Ser269.")
![Western Blot: LRP-1 Antibody [NBP2-62753] - Western blot analysis of Mouse, Rat Brain showing detection of 504.6 kDa LRP-1 protein using Rabbit Anti-LRP-1 Polyclonal Antibody (NBP2-62753). Lane 1: Molecular Weight Ladder (MW). Lane 2: Mouse Brain. Lane 3: Rat Brain . Load: 15 ug. Block: 5% Skim Milk powder in TBST. Primary Antibody: Rabbit Anti-LRP-1 Polyclonal Antibody (NBP2-62753) at 1:1000 for 2 hours at RT with shaking. Secondary Antibody: Goat Anti-Rabbit IgG: HRP at 1:5000 for 1 hour at RT. Color Development: ECL solution for 5 min at RT. Predicted/Observed Size: 504.6 kDa. Other Band(s): 80 kDa.](http://images.novusbio.com/fullsize/LRP-1-Antibody-Western-Blot-NBP2-62753-img0003.jpg "Western Blot: LRP-1 Antibody [NBP2-62753] - Western blot analysis of Mouse, Rat Brain showing detection of 504.6 kDa LRP-1 protein using Rabbit Anti-LRP-1 Polyclonal Antibody (NBP2-62753). Lane 1: Molecular Weight Ladder (MW). Lane 2: Mouse Brain. Lane 3: Rat Brain . Load: 15 ug. Block: 5% Skim Milk powder in TBST. Primary Antibody: Rabbit Anti-LRP-1 Polyclonal Antibody (NBP2-62753) at 1:1000 for 2 hours at RT with shaking. Secondary Antibody: Goat Anti-Rabbit IgG: HRP at 1:5000 for 1 hour at RT. Color Development: ECL solution for 5 min at RT. Predicted/Observed Size: 504.6 kDa. Other Band(s): 80 kDa.")
![Immunohistochemistry: LRP-1 Antibody [NBP2-62753] - Immunohistochemistry analysis using Rabbit Anti-LRP1 Polyclonal Antibody (NBP2-62753). Tissue: Liver. Species: Human. Fixation: Formalin Fixed Paraffin-Embedded. Primary Antibody: Rabbit Anti-LRP1 Polyclonal Antibody (NBP2-62753) at 1:50 for 30 min at RT. Counterstain: Hematoxylin. Magnification: 10X. HRP-DAB Detection.](http://images.novusbio.com/fullsize/LRP-1 Antibody-Immunohistochemistry-NBP2-62753-img0004.jpg)
![Western Blot: NMDAR2B [p Tyr1472] Antibody [NB300-182] - Rat hippocampal lysate showing specific immunolabeling of the ~180 kDa NR2B subunit of the NMDAR phosphorylated at Tyr1472 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by lysate treatment with lambda phosphatase (400 units/100uL lysate for 30 min).](http://images.novusbio.com/fullsize/NMDAR2B-[p-Tyr1472]-Antibody-Western-Blot-NB300-182-img0002.jpg "Western Blot: NMDAR2B [p Tyr1472] Antibody [NB300-182] - Rat hippocampal lysate showing specific immunolabeling of the ~180 kDa NR2B subunit of the NMDAR phosphorylated at Tyr1472 in the first lane (-). Phosphospecificity is shown in the second lane (+) where immunolabeling is completely eliminated by lysate treatment with lambda phosphatase (400 units/100uL lysate for 30 min).")
![Western Blot: SCL/Tal1 Antibody (1E6) [NBP2-50285] - Western Blotting on 293T cell lysates (transfected) using anti-SCL [1E6]. + refers to serum from immunized mouse.](http://images.novusbio.com/fullsize/SCL-Tal1-Antibody-1E6-Western-Blot-NBP2-50285-img0001.jpg "Western Blot: SCL/Tal1 Antibody (1E6) [NBP2-50285] - Western Blotting on 293T cell lysates (transfected) using anti-SCL [1E6]. + refers to serum from immunized mouse.")
![Immunocytochemistry/Immunofluorescence: SCL/Tal1 Antibody (1E6) [NBP2-50285] - Analysis of transfected 293T cells. DAPI (nucleus) counterstain is shown in blue.](http://images.novusbio.com/fullsize/SCL-Tal1-Antibody-1E6-Immunocytochemistry-Immunofluorescence-NBP2-50285-img0002.jpg)
![Western Blot: Progesterone Receptor [p Ser294] Antibody (608) [NB200-320] - Whole cell T47D lysate prepared from cells that had been incubated in the presence of the synthetic progestin agonist R5020 (500 nM) showing specific immunolabeling of the ~90k PR-A isoform and the ~120 PR-B isoform of the progesterone receptor phosphorylated at Ser294. The immunolabeling is blocked by the phosphopeptide used as the antigen (not shown).](http://images.novusbio.com/fullsize/Progesterone-Receptor-p-Ser294-Antibody-608-Western-Blot-NB200-320-img0001.jpg "Western Blot: Progesterone Receptor [p Ser294] Antibody (608) [NB200-320] - Whole cell T47D lysate prepared from cells that had been incubated in the presence of the synthetic progestin agonist R5020 (500 nM) showing specific immunolabeling of the ~90k PR-A isoform and the ~120 PR-B isoform of the progesterone receptor phosphorylated at Ser294. The immunolabeling is blocked by the phosphopeptide used as the antigen (not shown).")
![Immunohistochemistry-Paraffin: HSF1 Antibody (10H8) [NBP1-97504] - Analysis of human skeletal muscle tissue stained with HSF1, mAb (10H8) at 10ug/ml.](http://images.novusbio.com/fullsize/HSF1-Antibody-10H8-Immunohistochemistry-Paraffin-NBP1-97504-img0002.jpg "Immunohistochemistry-Paraffin: HSF1 Antibody (10H8) [NBP1-97504] - Analysis of human skeletal muscle tissue stained with HSF1, mAb (10H8) at 10ug/ml.")
![Western Blot: BNIP3 Antibody (ANa40) [NB100-1543] - Monoclonal Anti-BNIP3 antibody produced in mouse](http://images.novusbio.com/fullsize/BNIP3-Antibody-ANa40-Western-Blot-NB100-1543-img0001.jpg "Western Blot: BNIP3 Antibody (ANa40) [NB100-1543] - Monoclonal Anti-BNIP3 antibody produced in mouse")
![Immunohistochemistry-Paraffin: Polycystin-1/PKD1 Antibody [NBP1-52552] - Analysis of anti-PKD1 antibody with human kidney at concentration 3.75 ug/ml.](http://images.novusbio.com/fullsize/Polycystin-1-PKD1-Antibody-Immunohistochemistry-Paraffin-NBP1-52552-img0002.jpg "Immunohistochemistry-Paraffin: Polycystin-1/PKD1 Antibody [NBP1-52552] - Analysis of anti-PKD1 antibody with human kidney at concentration 3.75 ug/ml.")
![Immunohistochemistry-Paraffin: Polycystin-1/PKD1 Antibody [NBP1-52552] - Analysis of anti-PKD1 antibody with human spleen at concentration 3.75 ug/ml.](http://images.novusbio.com/fullsize/Polycystin-1-PKD1-Antibody-Immunohistochemistry-Paraffin-NBP1-52552-img0001.jpg)
![Western Blot: FADD Antibody (PSH01-13) [NBP3-32329] - Western blot analysis of FADD on different lysates with Rabbit anti-FADD antibody (NBP3-32329) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: A431 cell lysate Lane 3: MCF7 cell lysate Lane 4: A549 cell lysate Lane 5: HepG2 cell lysate Lane 6: Jurkat cell lysate Lane 7: SK-Br-3 cell lysate Lysates/proteins at 40 ug/Lane. Predicted band size: 23 kDa Observed band size: 28 kDa Exposure time: 1 minute 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 (NBP3-32329) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. 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/nbp3-32329_rabbit-fadd-mab-psh01-13-278202416331250.jpg "Western Blot: FADD Antibody (PSH01-13) [NBP3-32329] - Western blot analysis of FADD on different lysates with Rabbit anti-FADD antibody (NBP3-32329) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: A431 cell lysate Lane 3: MCF7 cell lysate Lane 4: A549 cell lysate Lane 5: HepG2 cell lysate Lane 6: Jurkat cell lysate Lane 7: SK-Br-3 cell lysate Lysates/proteins at 40 ug/Lane. Predicted band size: 23 kDa Observed band size: 28 kDa Exposure time: 1 minute 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 (NBP3-32329) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: FADD Antibody (PSH01-13) [NBP3-32329] - Immunocytochemistry analysis of A431 cells labeling FADD with Rabbit anti-FADD antibody (NBP3-32329) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-FADD antibody (NBP3-32329) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32329_rabbit-fadd-mab-psh01-13-29202410484814.jpg)
![Flow Cytometry: FADD Antibody (PSH01-13) [NBP3-32329] - Flow cytometric analysis of A431 cells labeling FADD. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32329, 1ug/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/nbp3-32329_rabbit-fadd-mab-psh01-13-29202416453276.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: SHIP Antibody (SHIP-01) [NB110-81538] - 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 Lane 2,3: immunostaining with anti-human SHIP-1 (SHIP-01) Lane 4,5: immunostaining with anti-human SHIP-1 (SHIP-02).](http://images.novusbio.com/fullsize/SHIP-Antibody-SHIP-01-Western-Blot-NB110-81538-img0001.jpg)
![Flow Cytometry: Mouse Monoclonal SHIP Antibody (SHIP-01) [NB110-81538] - Separation of MOLT-4 cells (red-filled) from CaCo-2 cells (black-dashed) in flow cytometry analysis (intracellular staining) of cellular suspensions of MOLT-4 and CaCo-2 cell lines stained using anti-SHIP (SHIP-01) purified antibody (concentration in sample 1 ug/ml, GAM APC).](http://images.novusbio.com/fullsize/antibody/nb110-81538_mouse-monoclonal-ship-antibody-ship-01-flow-cytometry-11122024124041..jpg)
![Immunohistochemistry: Chk1 [p Ser317] Antibody (PSH03-84) [NBP3-32755] - Immunohistochemical analysis of paraffin-embedded HeLa cells treated with or without UV for 40 minutes with Rabbit anti-Chk1 antibody (NBP3-32755) 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 (NBP3-32755) 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/nbp3-32755_rabbit-chk1-p-ser317-mab-psh03-84-298202414262624.jpg "Immunohistochemistry: Chk1 [p Ser317] Antibody (PSH03-84) [NBP3-32755] - Immunohistochemical analysis of paraffin-embedded HeLa cells treated with or without UV for 40 minutes with Rabbit anti-Chk1 antibody (NBP3-32755) 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 (NBP3-32755) 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.")
![Western Blot: Chk1 [p Ser317] Antibody (PSH03-84) [NBP3-32755] - Western blot analysis of Chk1 on different lysates with Rabbit anti-Chk1 antibody (NBP3-32755) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: HeLa treated with UV for 1 hour cell lysate Lane 3: C6 cell lysate Lane 4: C6 treated with 100nM Calyculin A for 30 minutes cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 54 kDa Observed band size: 54 kDa Exposure time: 43 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 at 1/1,000 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/nbp3-32755_rabbit-chk1-p-ser317-mab-psh03-84-392024848501.jpg)