| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05539-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-05081-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90437-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12073-0.025mg | |||
![Western Blot: SR-AI/MSR Antibody (A8G2-R) [NBP3-32134] - Western blot analysis of SR-AI/MSR on different lysates with Mouse anti-SR-AI/MSR antibody (NBP3-32134) at 1/1,000 dilution. Lane 1: THP-1 treated with 50ng/mL PMA for 72 hours whole cell lysate Lane 2: THP-1 whole cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 50 kDa Observed band size: 75 kDa Exposure time: 50 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 (NBP3-32134) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32134_mouse-sr-ai-msr-mab-a8g2-r-27820241521242.jpg "Western Blot: SR-AI/MSR Antibody (A8G2-R) [NBP3-32134] - Western blot analysis of SR-AI/MSR on different lysates with Mouse anti-SR-AI/MSR antibody (NBP3-32134) at 1/1,000 dilution. Lane 1: THP-1 treated with 50ng/mL PMA for 72 hours whole cell lysate Lane 2: THP-1 whole cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 50 kDa Observed band size: 75 kDa Exposure time: 50 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 (NBP3-32134) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: SR-AI/MSR Antibody (A8G2-R) [NBP3-32134] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-SR-AI/MSR antibody (NBP3-32134) at 1μg/mL 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 (NBP3-32134) at 1μg/mL 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/nbp3-32134_mouse-sr-ai-msr-mab-a8g2-r-2982024143522.jpg)
![Immunocytochemistry/ Immunofluorescence: SR-AI/MSR Antibody (A8G2-R) [NBP3-32134] - Immunocytochemistry analysis of THP-1 cells treated with or without 50ng/mL PMA for 72 hours labeling SR-AI/MSR with Mouse anti-SR-AI/MSR antibody (NBP3-32134) 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 Mouse anti-SR-AI/MSR antibody (NBP3-32134) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse 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-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32134_mouse-sr-ai-msr-mab-a8g2-r-2920241192356.jpg)
![Western Blot: ABCB9 Antibody [NBP1-18886] - Whole cell lysate from HeLa (5, 15 and 50 ug for WB; 1 mg for IP, 20%of IP loaded), HEK293T (T; 50 ug) and mouse NIH 3T3 (M; 50ug) cells. Antibodies: Affinity purified rabbit anti-ABCB9 antibody used for WB at 0.04 ug/ml (A) and 1ug/ml (B) and used for IP at 3 ug/mg lysate. Detection: Chemiluminescence with exposure times of 10 seconds (A) and 3 seconds (B).](http://images.novusbio.com/fullsize/ABCB9-Antibody-Western-Blot-NBP1-18886-img0010.jpg "Western Blot: ABCB9 Antibody [NBP1-18886] - Whole cell lysate from HeLa (5, 15 and 50 ug for WB; 1 mg for IP, 20%of IP loaded), HEK293T (T; 50 ug) and mouse NIH 3T3 (M; 50ug) cells. Antibodies: Affinity purified rabbit anti-ABCB9 antibody used for WB at 0.04 ug/ml (A) and 1ug/ml (B) and used for IP at 3 ug/mg lysate. Detection: Chemiluminescence with exposure times of 10 seconds (A) and 3 seconds (B).")
![Immunohistochemistry-Paraffin: ABCB9 Antibody [NBP1-18886] - Human prostate carcinoma. Antibody used at a dilution of 1:200 (1ug/ml).](http://images.novusbio.com/fullsize/ABCB9-Antibody-Immunohistochemistry-Paraffin-NBP1-18886-img0009.jpg)
![Western Blot: PKLR Antibody [NBP1-32314] - Sample (50 ug of whole cell lysate) A: mouse liver 7. 5% SDS PAGE; antibody diluted at 1:500.](http://images.novusbio.com/fullsize/PKLR-Antibody-Western-Blot-NBP1-32314-img0007.jpg "Western Blot: PKLR Antibody [NBP1-32314] - Sample (50 ug of whole cell lysate) A: mouse liver 7. 5% SDS PAGE; antibody diluted at 1:500.")
![Western Blot: PKLR Antibody [NBP1-32314] - 30 ug Raw264. 7 whole cell lysate/extract 7. 5 % SDS-PAGE gel, antibody dilution 1:1000.](http://images.novusbio.com/fullsize/PKLR-Antibody-Western-Blot-NBP1-32314-img0008.jpg)
![Western Blot: PKLR Antibody [NBP1-32314] - A. 30 ug K562 whole cell lysate/extract 7. 5 % SDS-PAGE gel, antibody dilution 1:1000.](http://images.novusbio.com/fullsize/PKLR-Antibody-Western-Blot-NBP1-32314-img0009.jpg)
![Western Blot: PKLR Antibody [NBP1-32314] - PKLR antibody detects PKLR protein by western blot analysis.A. 30 ug 293T whole cell lysate/extract B. 5 ug whole cell lysate/extract of human PKLR-transfected 293T cells7.5 % SDS-PAGEPKLR antibody (NBP1-32314) dilution: 1:10000](http://images.novusbio.com/fullsize/nbp1-32314_rabbit-polyclonal-pklr-antibody-910202420134088.jpg)
![Western Blot: 15-Lipoxygenase 1 Antibody [H00000246-D01P] - Analysis of ALOX15 expression in mouse spleen.](http://images.novusbio.com/fullsize/15-Lipoxygenase-1-Antibody-Western-Blot-H00000246-D01P-img0003.jpg "Western Blot: 15-Lipoxygenase 1 Antibody [H00000246-D01P] - Analysis of ALOX15 expression in mouse spleen.")
![Western Blot: 15-Lipoxygenase 1 Antibody [H00000246-D01P] - Analysis of ALOX15 expression in transfected 293T cell line by ALOX15 polyclonal antibody.Lane 1: ALOX15 transfected lysate(74.80 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/15-Lipoxygenase-1-Antibody-Western-Blot-H00000246-D01P-img0004.jpg)
![Western Blot: MARCKS Antibody [NBP3-05540] - Western blot analysis of different cell lines lysates using MARCKS, at a dilution of 1:1,000 in green: [1] protein standard (red), [2] HEK293, [3] HeLa, [4] SH-SY5Y, and [5] COS1 cells. Strong band at 80kDa corresponds to MARCKS protein. The same blot was simultaneously probed with mouse mAb to GAPDH at a dilution of 1:5,000 in red, which reveals a single band at 37kDa in all preparations.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Western-Blot-NBP3-05540-img0002.jpg "Western Blot: MARCKS Antibody [NBP3-05540] - Western blot analysis of different cell lines lysates using MARCKS, at a dilution of 1:1,000 in green: [1] protein standard (red), [2] HEK293, [3] HeLa, [4] SH-SY5Y, and [5] COS1 cells. Strong band at 80kDa corresponds to MARCKS protein. The same blot was simultaneously probed with mouse mAb to GAPDH at a dilution of 1:5,000 in red, which reveals a single band at 37kDa in all preparations.")
![Immunocytochemistry/Immunofluorescence: MARCKS Antibody [NBP3-05540] - Immunofluorescent analysis of HeLa cells stained with MARCKS Antibody at a dilution of 1:5,000 in red, and costained with mouse mAb to beta-tubulin at a dilution of 1:10,000 in green. The blue is Hoechst staining of nuclear DNA. The MARCKS antibody binds to MARCKS protein expressed in the plasma membrane and cytoplasm, while the beta-tubulin antibody stains cytoplasmic microtubules.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05540-img0001.jpg)
![Western Blot: MARCKS Antibody [NBP3-05539] - Western blot analysis of different cell lysates using MARCKS Antibody in green: [1] protein standard, [2] NIH-3T3, [3] HEK293, [4] HeLa, [5] SH-SY5Y, [6] C6 and [7] COS1 cells. The band at about 80kDa corresponds to the MARCKS protein detected only in the human and monkey cells. The antibody does not recognize the rodent form of the MARCKS protein.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Western-Blot-NBP3-05539-img0002.jpg "Western Blot: MARCKS Antibody [NBP3-05539] - Western blot analysis of different cell lysates using MARCKS Antibody in green: [1] protein standard, [2] NIH-3T3, [3] HEK293, [4] HeLa, [5] SH-SY5Y, [6] C6 and [7] COS1 cells. The band at about 80kDa corresponds to the MARCKS protein detected only in the human and monkey cells. The antibody does not recognize the rodent form of the MARCKS protein.")
![Immunocytochemistry/Immunofluorescence: MARCKS Antibody [NBP3-05539] - Immunofluorescent analysis of HeLa cell culture stained with MARCKS Antibody at a dilution of 1:1,000 in red, and costained with chicken pAb to vimentin at a dilution of 1:10,000 in green. The blue is Hoechst staining of nuclear DNA. MARCKS antibody binds to MARCKS protein expressed in the membrane structures and in cytoplasm, while the vimentin antibody stains the intermediate filaments.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05539-img0001.jpg)
![Western Blot: INPP5E Antibody [NBP3-05081] - Analysis of extracts of SH-SY5Y cells, using INPP5E 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. Detection: ECL Basic Kit](http://images.novusbio.com/fullsize/INPP5E-Antibody-Western-Blot-NBP3-05081-img0003.jpg "Western Blot: INPP5E Antibody [NBP3-05081] - Analysis of extracts of SH-SY5Y cells, using INPP5E 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. Detection: ECL Basic Kit")
![Immunocytochemistry/Immunofluorescence: INPP5E Antibody [NBP3-05081] - Analysis of L929 cells using INPP5E antibody at dilution of 1:100. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/INPP5E-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05081-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: INPP5E Antibody [NBP3-05081] - Analysis of C6 cells using INPP5E antibody at dilution of 1:100. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/INPP5E-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05081-img0001.jpg)
![Western Blot: SR-AI/MSR Antibody (10O8B0) [NBP3-16126] - Western blot analysis of extracts of various cell lines, using SR-AI/MSR antibody (NBP3-16126) at 1:1000 dilution.C6 cells were treated by LPS for 6 hours and Brefeldin A for 3 hours of stimulation. 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: 10s.](http://images.novusbio.com/fullsize/SR-AI-MSR-Antibody-10O8B0-Western-Blot-NBP3-16126-img0003.jpg "Western Blot: SR-AI/MSR Antibody (10O8B0) [NBP3-16126] - Western blot analysis of extracts of various cell lines, using SR-AI/MSR antibody (NBP3-16126) at 1:1000 dilution.C6 cells were treated by LPS for 6 hours and Brefeldin A for 3 hours of stimulation. 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: 10s.")
![Immunohistochemistry-Paraffin: SR-AI/MSR Antibody (10O8B0) [NBP3-16126] - Immunohistochemistry of paraffin-embedded mouse testis using SR-AI/MSR Rabbit mAb (NBP3-16126) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/SR-AI-MSR-Antibody-10O8B0-Immunohistochemistry-Paraffin-NBP3-16126-img0002.jpg)
![Immunohistochemistry-Paraffin: SR-AI/MSR Antibody (10O8B0) [NBP3-16126] - Immunohistochemistry of paraffin-embedded rat brain using SR-AI/MSR Rabbit mAb (NBP3-16126) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/SR-AI-MSR-Antibody-10O8B0-Immunohistochemistry-Paraffin-NBP3-16126-img0001.jpg)
![Immunohistochemistry-Paraffin: SR-AI/MSR Antibody (004) [NBP2-90437] - Immunochemical staining of mouse SR-AI/MSR in mouse liver with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/SR-AI-MSR-Antibody-004-Immunohistochemistry-Paraffin-NBP2-90437-img0003.jpg "Immunohistochemistry-Paraffin: SR-AI/MSR Antibody (004) [NBP2-90437] - Immunochemical staining of mouse SR-AI/MSR in mouse liver with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).")
![Flow Cytometry: SR-AI/MSR Antibody (004) [NBP2-90437] - Flow cytometric analysis of Mouse SR-AI/MSR expression on Raw264.7 cells. Cells were stained with purified anti-Mouse SR-AI/MSR, 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/SR-AI-MSR-Antibody-004-Flow-Cytometry-NBP2-90437-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: SR-AI/MSR Antibody (004) [NBP2-90437] - Confocal immunofluorescence analysis of Mouse SR-AI/MSR1 in RAW264.7 cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90437 antibody (1:100) 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 plasma membrane.](http://images.novusbio.com/fullsize/nbp2-90437_rabbit-monoclonal-sr-ai-msr-antibody-004-235202511444470.png)
![Western Blot: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Western blot analysis of Myeloperoxidase/MPO on different lysates with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/5,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 84 kDa Observed band size: 84/55 kDa Exposure time: 24 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 (NBP3-32624) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C 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/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-2882024142265.jpg "Western Blot: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Western blot analysis of Myeloperoxidase/MPO on different lysates with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/5,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 84 kDa Observed band size: 84/55 kDa Exposure time: 24 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 (NBP3-32624) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) 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 (NBP3-32624) 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/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-298202414161865.jpg)
![Immunocytochemistry/ Immunofluorescence: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Immunocytochemistry analysis of Jurkat cells labeling Myeloperoxidase/MPO with Rabbit anti-Myeloperoxidase/MPO/MPO antibody (NBP3-32624) at 1/100 dilution. Cells were fixed in 80% 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-Myeloperoxidase/MPO antibody (NBP3-32624) 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/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-29202410234294.jpg)
![Western Blot: SR-BI Antibody (185-1G2 (B467)) - Chimeric [NBP3-12073] - Human peripheral blood monocyte cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 185-1G2 (B467) (NBP3-12073) at 0.03 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.](http://images.novusbio.com/fullsize/SR-BI-Antibody-185-1G2-B467-Chimeric-Western-Blot-NBP3-12073-img0001.jpg "Western Blot: SR-BI Antibody (185-1G2 (B467)) - Chimeric [NBP3-12073] - Human peripheral blood monocyte cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 185-1G2 (B467) (NBP3-12073) at 0.03 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.")
![Immunocytochemistry /Immunofluorescence: SR-BI Antibody (185-1G2 (B467)) - Chimeric - Azide and BSA Free [NBP3-12073] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on Shi-fix(TM) coverslips stained with NBP3-12073 at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12073, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-12073_rabbit-monoclonal-sr-bi-antibody-185-1g2-b467-chimeric-74202522141242.png)
![Western Blot: Glutathione Peroxidase 7 Antibody [NBP1-31474] - Analysis of GPX7 expression in transfected 293T cell line by GPX7 polyclonal antibody. A: Non-transfected lysate. B: GPX7 transfected lysate. 12% SDS PAGE, antibody diluted at 1:500.](http://images.novusbio.com/fullsize/Glutathione-Peroxidase-7-Antibody-Western-Blot-NBP1-31474-img0004.jpg "Western Blot: Glutathione Peroxidase 7 Antibody [NBP1-31474] - Analysis of GPX7 expression in transfected 293T cell line by GPX7 polyclonal antibody. A: Non-transfected lysate. B: GPX7 transfected lysate. 12% SDS PAGE, antibody diluted at 1:500.")
![Immunohistochemistry-Paraffin: Glutathione Peroxidase 7 Antibody [NBP1-31474] - Mouse esophagus. GPX7 antibody [N1C3] diluted at 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min](http://images.novusbio.com/fullsize/Glutathione-Peroxidase-7-Antibody-Immunohistochemistry-Paraffin-NBP1-31474-img0005.jpg)
![Immunohistochemistry-Paraffin: Glutathione Peroxidase 7 Antibody [NBP1-31474] - H441 xenograft, using GPX7 antibody at 1:100 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min](http://images.novusbio.com/fullsize/Glutathione-Peroxidase-7-Antibody-Immunohistochemistry-Paraffin-NBP1-31474-img0003.jpg)