| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21199-25ul | |||
| Azide and BSA Free | NBP3-44138 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-15122-25ul | |||
| Azide and BSA Free | NBP3-44184 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-12889-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-35132-20ul | |||
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (CL11661) [NBP3-15122] - Staining of human spleen shows strong granular cytoplasmic positivity in cells in red pulp.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-CL11661-Immunohistochemistry-Paraffin-NBP3-15122-img0004.jpg "Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (CL11661) [NBP3-15122] - Staining of human spleen shows strong granular cytoplasmic positivity in cells in red pulp.")
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (CL11661) [NBP3-15122] - Staining of human fallopian tube shows no positivity in glandular cells as expected.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-CL11661-Immunohistochemistry-Paraffin-NBP3-15122-img0001.jpg)
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (CL11661) [NBP3-15122] - Staining of human prostate shows no positivity in glandular cells as expected.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-CL11661-Immunohistochemistry-Paraffin-NBP3-15122-img0002.jpg)
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (CL11661) [NBP3-15122] - Staining of human skeletal muscle shows no positivity in myocytes as expected.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-CL11661-Immunohistochemistry-Paraffin-NBP3-15122-img0003.jpg)
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (CL11661) [NBP3-15122] - Analysis in human spleen and skeletal muscle tissues using NBP3-15122 antibody. Corresponding HMOX1 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-CL11661-Immunohistochemistry-Paraffin-NBP3-15122-img0005.jpg)
![Western Blot: GRP78/HSPA5 Antibody (6H4-2G7) [NBP2-12889] - analysis of Human recombinant cell lysate showing detection of GRP78 protein using Mouse Anti-GRP78 Monoclonal Antibody, Clone 6H4.2G7 . Primary Antibody: Mouse Anti-GRP78 Monoclonal Antibody at 1:1000.](http://images.novusbio.com/fullsize/GRP78-HSPA5-Antibody-6H4-2G7-Western-Blot-NBP2-12889-img0002.jpg "Western Blot: GRP78/HSPA5 Antibody (6H4-2G7) [NBP2-12889] - analysis of Human recombinant cell lysate showing detection of GRP78 protein using Mouse Anti-GRP78 Monoclonal Antibody, Clone 6H4.2G7 . Primary Antibody: Mouse Anti-GRP78 Monoclonal Antibody at 1:1000.")
![Immunocytochemistry/Immunofluorescence: GRP78/HSPA5 Antibody (6H4-2G7) [NBP2-12889] - Tissue: Cervical Cancer cell line (HeLa). Species: Human. Fixation: 4% Formaldehyde for 15 min at RT. Primary Antibody: Mouse Anti-GRP78 Monoclonal Antibody at 1:100 for 60 min at RT. Secondary Antibody: Goat Anti-Mouse ATTO 488 at 1:100 for 60 min at RT. Counterstain: DAPI (blue) nuclear stain at 1:5000 for 5 min RT. Localization: Endoplasmic Reticulum, Endoplasmic Reticulum Lumen. Magnification: 60X.](http://images.novusbio.com/fullsize/GRP78-HSPA5-Antibody-6H4-2G7-Immunocytochemistry-Immunofluorescence-NBP2-12889-img0003.jpg)
![Western Blot: iNOS Antibody (PSH03-69) [NBP3-32473] - Western blot analysis of iNOS on different lysates with Rabbit anti-iNOS antibody (NBP3-32473) at 1/1,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 1ug/mL LPS for 24 hours cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 131 kDa Observed band size: 131 kDa Exposure time: 3 minutes; ECL; 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 (NBP3-32473) 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/nbp3-32473_rabbit-inos-mab-psh03-69-278202415295526.jpg "Western Blot: iNOS Antibody (PSH03-69) [NBP3-32473] - Western blot analysis of iNOS on different lysates with Rabbit anti-iNOS antibody (NBP3-32473) at 1/1,000 dilution. Lane 1: RAW264.7 cell lysate Lane 2: RAW264.7 treated with 1ug/mL LPS for 24 hours cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 131 kDa Observed band size: 131 kDa Exposure time: 3 minutes; ECL; 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 (NBP3-32473) 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.")
![Immunohistochemistry: iNOS Antibody (PSH03-69) [NBP3-32473] - Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue with Rabbit anti-iNOS antibody (NBP3-32473) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (NBP3-32473) at 1/200 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/nbp3-32473_rabbit-inos-mab-psh03-69-298202414304151.jpg)
![Immunocytochemistry/ Immunofluorescence: iNOS Antibody (PSH03-69) [NBP3-32473] - Immunocytochemistry analysis of RAW264.7 cells treated with or without 1μg/mL LPS for 6 hours labeling iNOS with Rabbit anti-iNOS antibody (NBP3-32473) at 1/100 dilution. Cells were fixed in 100% precooled methanol 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-iNOS antibody (NBP3-32473) 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/nbp3-32473_rabbit-inos-mab-psh03-69-29202410334018.jpg)
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (SP08-07) [NBP2-67382] - Analysis of paraffin-embedded mouse liver tissue using anti-HO-1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-SP08-07-Immunohistochemistry-Paraffin-NBP2-67382-img0004.jpg "Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (SP08-07) [NBP2-67382] - Analysis of paraffin-embedded mouse liver tissue using anti-HO-1 antibody. Counter stained with hematoxylin.")
![Flow Cytometry: HO-1/HMOX1/HSP32 Antibody (SP08-07) [NBP2-67382] - Analysis of Jurkat cells with HO-1 antibody at 1/50 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 secondary antibody.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-SP08-07-Flow-Cytometry-NBP2-67382-img0001.jpg)
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (SP08-07) [NBP2-67382] - Analysis of paraffin-embedded human liver tissue using anti-HO-1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-SP08-07-Immunohistochemistry-Paraffin-NBP2-67382-img0002.jpg)
![Immunohistochemistry-Paraffin: HO-1/HMOX1/HSP32 Antibody (SP08-07) [NBP2-67382] - Analysis of paraffin-embedded human spleen tissue using anti-HO-1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/HO-1-HMOX1-HSP32-Antibody-SP08-07-Immunohistochemistry-Paraffin-NBP2-67382-img0003.jpg)
![Western Blot: HO-1/HMOX1/HSP32 Antibody (PSH02-76) [NBP3-32420] - Western blot analysis of HO-1/HMOX1/HSP32 on different lysates with Rabbit anti-HO-1/HMOX1/HSP32 antibody (NBP3-32420) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: A549 cell lysate Lane 3: RAW264.7 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 33 kDa Observed band size: 33 kDa Exposure time: 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 (NBP3-32420) 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 1/200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32420_rabbit-ho-1-hmox1-hsp32-mab-psh02-76-27820241524263.jpg "Western Blot: HO-1/HMOX1/HSP32 Antibody (PSH02-76) [NBP3-32420] - Western blot analysis of HO-1/HMOX1/HSP32 on different lysates with Rabbit anti-HO-1/HMOX1/HSP32 antibody (NBP3-32420) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: A549 cell lysate Lane 3: RAW264.7 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 33 kDa Observed band size: 33 kDa Exposure time: 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 (NBP3-32420) 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 1/200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: HO-1/HMOX1/HSP32 Antibody (PSH02-76) [NBP3-32420] - Immunohistochemical analysis of paraffin-embedded human renal cell carcinoma tissue with Rabbit anti-HO-1/HMOX1/HSP32 antibody (NBP3-32420) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (NBP3-32420) 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/nbp3-32420_rabbit-ho-1-hmox1-hsp32-mab-psh02-76-298202414262647.jpg)
![Immunocytochemistry/ Immunofluorescence: HO-1/HMOX1/HSP32 Antibody (PSH02-76) [NBP3-32420] - Immunocytochemistry analysis of A549 cells labeling HO-1/HMOX1/HSP32 with Rabbit anti-HO-1/HMOX1/HSP32 antibody (NBP3-32420) 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-HO-1/HMOX1/HSP32 antibody (NBP3-32420) 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/nbp3-32420_rabbit-ho-1-hmox1-hsp32-mab-psh02-76-29202410484883.jpg)
![Western Blot: Carbonic Anhydrase I/CA1 Antibody [H00000759-D01P] - Analysis of CA1 expression in mouse brain.](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-I-CA1-Antibody-Western-Blot-H00000759-D01P-img0005.jpg "Western Blot: Carbonic Anhydrase I/CA1 Antibody [H00000759-D01P] - Analysis of CA1 expression in mouse brain.")
![Western Blot: Carbonic Anhydrase I/CA1 Antibody [H00000759-D01P] - Analysis of CA1 expression in human colon.](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-I-CA1-Antibody-Western-Blot-H00000759-D01P-img0003.jpg)
![Western Blot: Carbonic Anhydrase I/CA1 Antibody [H00000759-D01P] - Analysis of CA1 expression in human placenta.](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-I-CA1-Antibody-Western-Blot-H00000759-D01P-img0004.jpg)
![Western Blot: Carbonic Anhydrase I/CA1 Antibody [H00000759-D01P] - Analysis of CA1 expression in transfected 293T cell line by CA1 polyclonal antibody.Lane 1: CA1 transfected lysate(28.90 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-I-CA1-Antibody-Western-Blot-H00000759-D01P-img0006.jpg)
![Western Blot: CUGBP2 Antibody [NBP1-57376] - Sample Tissue: Human 293T Antibody Dilution: 1.0 ug/ml](http://images.novusbio.com/fullsize/CUGBP2-Antibody-Western-Blot-NBP1-57376-img0007.jpg "Western Blot: CUGBP2 Antibody [NBP1-57376] - Sample Tissue: Human 293T Antibody Dilution: 1.0 ug/ml")
![Immunohistochemistry: CUGBP2 Antibody [NBP1-57376] - Paraffin Embedded Tissue: Human Heart Cellular Data: Myocardial cells Antibody Concentration: 4.0 - 8.0 ug/ml Magnification: 400X](http://images.novusbio.com/fullsize/CUGBP2-Antibody-Immunohistochemistry-NBP1-57376-img0006.jpg)
![Western Blot: CUGBP2 Antibody [NBP1-57376] - Reccomended Titration: 1.25 ug/ml ELISA Titer: 1:312500 Positive Control: Jurkat cell lysate CELF2 is strongly supported by BioGPS gene expression data to be expressed in Human Jurkat cells](http://images.novusbio.com/fullsize/CUGBP2-Antibody-Western-Blot-NBP1-57376-img0008.jpg)
![Immunohistochemistry: CUGBP2 Antibody [NBP1-57376] - Paraffin Embedded Tissue: Human alveolar cell Cellular Data: Epithelial cells of renal tubule Antibody Concentration: 4.0 - 8.0 ug/ml Magnification: 400X](http://images.novusbio.com/fullsize/CUGBP2-Antibody-Immunohistochemistry-NBP1-57376-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: xCT Antibody [NB100-59735] - Immunofluorescence analysis of paraformaldehyde fixed A549 cells,permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL). The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/xCT-Antibody-Immunocytochemistry-Immunofluorescence-NB100-59735-img0001.jpg "Immunocytochemistry/Immunofluorescence: xCT Antibody [NB100-59735] - Immunofluorescence analysis of paraformaldehyde fixed A549 cells,permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL). The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).")
![Immunocytochemistry/Immunofluorescence: xCT Antibody [NB100-59735] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing vesicle staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/xCT-Antibody-Immunocytochemistry-Immunofluorescence-NB100-59735-img0002.jpg)
![Western Blot: Carbonic Anhydrase I/CA1 Antibody [NBP1-36740] - (0.03ug/ml) staining of Human Liver lysate (35ug protein in RIPA buffer). Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-I-CA1-Antibody-Western-Blot-NBP1-36740-img0002.jpg "Western Blot: Carbonic Anhydrase I/CA1 Antibody [NBP1-36740] - (0.03ug/ml) staining of Human Liver lysate (35ug protein in RIPA buffer). Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: Carbonic Anhydrase I/CA1 Antibody [NBP1-36740] - (2.5ug/ml) staining of paraffin embedded Human Spleen. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.Click](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-I-CA1-Antibody-Immunohistochemistry-Paraffin-NBP1-36740-img0001.jpg)
![Western Blot: FAAH Antibody (10A1M7) [NBP3-16330] - Western blot analysis of extracts of various cell lines, using FAAH Rabbit mAb (NBP3-16330) 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: 30s.](http://images.novusbio.com/fullsize/FAAH-Antibody-10A1M7-Western-Blot-NBP3-16330-img0003.jpg)
![Immunocytochemistry/ Immunofluorescence: FAAH Antibody (10A1M7) [NBP3-16330] - Confocal imaging of NIH/3T3 cells using FAAH Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L).The cells were counterstained with alpha-Tubulin Mouse mAb followed by incubation with ABflo(R) 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (Green).DAPI was used for nuclear staining (Blue). Objective: 100x.](http://images.novusbio.com/fullsize/nbp3-16330_rabbit-faah-mab-10a1m7-5220251255582.jpg)
![Immunocytochemistry/ Immunofluorescence: GCLC Antibody [NBP3-35132] - Immunofluorescence analysis of PC-12 cells using GCLC Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-35132_rabbit-gclc-pab-101220241136093.jpg "Immunocytochemistry/ Immunofluorescence: GCLC Antibody [NBP3-35132] - Immunofluorescence analysis of PC-12 cells using GCLC Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.")
![Immunocytochemistry/ Immunofluorescence: GCLC Antibody [NBP3-35132] - Immunofluorescence analysis of Jurkat cells using GCLC Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-35132_rabbit-gclc-pab-1012202411433430.jpg)
![Western Blot: GCLC Antibody [NBP3-35132] - Western blot analysis of various lysates, using GCLC Rabbit pAb at 1:1000 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: 1s.](http://images.novusbio.com/fullsize/nbp3-35132_rabbit-gclc-pab-1012202411343339.jpg)