| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-08705 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-76600-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-77207-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-38537-20ul | |||
![Western Blot: NQO-1 Antibody (13A1) [NBP2-80395] - Analysis of NQO-1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody was used at a 1:5,000 dilution in 5% BSA at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:5,000 dilution was used for 1 hour at room temperature.Positive control: Lane 1: SiHa cell lysate, untreated Lane 2: A549 cell lysate, untreated](http://images.novusbio.com/fullsize/NQO-1-Antibody-13A1-Western-Blot-NBP2-80395-img0002.jpg "Western Blot: NQO-1 Antibody (13A1) [NBP2-80395] - Analysis of NQO-1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody was used at a 1:5,000 dilution in 5% BSA at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:5,000 dilution was used for 1 hour at room temperature.Positive control: Lane 1: SiHa cell lysate, untreated Lane 2: A549 cell lysate, untreated")
![Immunohistochemistry-Paraffin: NQO-1 Antibody (13A1) [NBP2-80395] - Immunohistochemical analysis of paraffin-embedded rat uterus tissue using anti-NQO-1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes. The tissues were blocked in 5% BSA for 30 m](http://images.novusbio.com/fullsize/NQO-1-Antibody-13A1-Immunohistochemistry-Paraffin-NBP2-80395-img0003.jpg)
![Immunohistochemistry-Paraffin: NQO-1 Antibody (13A1) [NBP2-80395] - Analysis in human kidney tissue using NQO-1 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with](http://images.novusbio.com/fullsize/NQO-1-Antibody-13A1-Immunohistochemistry-Paraffin-NBP2-80395-img0001.jpg)
![Western Blot: alcohol dehydrogenase 1C Antibody [H00000126-D01P] - Analysis of ADH1C expression in mouse liver.](http://images.novusbio.com/fullsize/alcohol-dehydrogenase-1C-Antibody-Western-Blot-H00000126-D01P-img0004.jpg "Western Blot: alcohol dehydrogenase 1C Antibody [H00000126-D01P] - Analysis of ADH1C expression in mouse liver.")
![Western Blot: alcohol dehydrogenase 1C Antibody [H00000126-D01P] - Analysis of ADH1C expression in Raw 264.7.](http://images.novusbio.com/fullsize/alcohol-dehydrogenase-1C-Antibody-Western-Blot-H00000126-D01P-img0002.jpg)
![Western Blot: alcohol dehydrogenase 1C Antibody [H00000126-D01P] - Analysis of ADH1C expression in human liver.](http://images.novusbio.com/fullsize/alcohol-dehydrogenase-1C-Antibody-Western-Blot-H00000126-D01P-img0003.jpg)
![Western Blot: alcohol dehydrogenase 1C Antibody [H00000126-D01P] - Analysis of ADH1C expression in transfected 293T cell line by ADH1C polyclonal antibody.Lane 1: ADH1C transfected lysate(39.90 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/alcohol-dehydrogenase-1C-Antibody-Western-Blot-H00000126-D01P-img0005.jpg)
![Western Blot: TRIM5 alpha Antibody [NBP1-76600] - Analysis of TRIM5 a expression in human stomach (A), thymus (B), and uterus (C) cell lysate with anti-TRIM5 a using this antibody at 2 ug/ml.](http://images.novusbio.com/fullsize/TRIM5-alpha-Antibody-Western-Blot-NBP1-76600-img0003.jpg "Western Blot: TRIM5 alpha Antibody [NBP1-76600] - Analysis of TRIM5 a expression in human stomach (A), thymus (B), and uterus (C) cell lysate with anti-TRIM5 a using this antibody at 2 ug/ml.")
![Immunocytochemistry/ Immunofluorescence: TRIM5 alpha Antibody - BSA Free [NBP1-76600] - Immunofluorescence of TRIM5 alpha in human breast tissue with TRIM5 alpha antibody at 10 ug/mL.](http://images.novusbio.com/fullsize/nbp1-76600_rabbit-polyclonal-trim5-alpha-antibody-271120241932648.jpg)
![Western Blot: TRIM5 alpha Antibody [NBP1-77207] - Western blot analysis of TRIM5 alpha expression in (A) human stomach (B) thymus, and (C) uterus tissue lysate with TRIM5 alpha antibody at 2 ug/ml.](http://images.novusbio.com/fullsize/TRIM5-alpha-Antibody-Western-Blot-NBP1-77207-img0003.jpg "Western Blot: TRIM5 alpha Antibody [NBP1-77207] - Western blot analysis of TRIM5 alpha expression in (A) human stomach (B) thymus, and (C) uterus tissue lysate with TRIM5 alpha antibody at 2 ug/ml.")
![Western Blot: TRIM5 alpha Antibody [NBP1-77207] - Human stomach (A), thymus (B), and uterus (C) cell lysate with TRIM5 alpha antibody at 2 ug /ml.](http://images.novusbio.com/fullsize/TRIM5-alpha-Antibody-Western-Blot-NBP1-77207-img0001.jpg)
![Immunohistochemistry: TRIM5 alpha Antibody - BSA Free [NBP1-77207] - Immunohistochemistry of TRIM5 alpha in human uterus tissue with TRIM5 alpha antibody at 2 ug/mL.](http://images.novusbio.com/fullsize/nbp1-77207_rabbit-polyclonal-trim5-alpha-antibody-2711202419392729.jpg)
![Western Blot: FBPase 1 Antibody [NBP1-55293] - Jurkat tissue lysate at a concentration of 1.25ug/ml.](http://images.novusbio.com/fullsize/FBPase-1-Antibody-Western-Blot-NBP1-55293-img0001.jpg "Western Blot: FBPase 1 Antibody [NBP1-55293] - Jurkat tissue lysate at a concentration of 1.25ug/ml.")
![Immunohistochemistry: FBPase 1 Antibody [NBP1-55293] - 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/FBPase-1-Antibody-Immunohistochemistry-NBP1-55293-img0003.jpg)
![Immunohistochemistry-Paraffin: FBPase 1 Antibody [NBP1-55293] - Human kidney Tissue, antibody concentration 4-8ug/ml. Cells with positive label: renal corpuscle cells (indicated with arrows) 400X magnification.](http://images.novusbio.com/fullsize/FBPase-1-Antibody-Immunohistochemistry-Paraffin-NBP1-55293-img0002.jpg)
![Western Blot: hydroxysteroid (17-beta) dehydrogenase 11 Antibody [NBP1-57081] - COLO205 cells lysate, concentration 0.2-1 ug/ml.](http://images.novusbio.com/fullsize/hydroxysteroid-17-beta-dehydrogenase-11-Antibody-Western-Blot-NBP1-57081-img0002.jpg "Western Blot: hydroxysteroid (17-beta) dehydrogenase 11 Antibody [NBP1-57081] - COLO205 cells lysate, concentration 0.2-1 ug/ml.")
![Immunohistochemistry-Paraffin: hydroxysteroid (17-beta) dehydrogenase 11 Antibody [NBP1-57081] - Monkey adrenal gland.](http://images.novusbio.com/fullsize/hydroxysteroid-17-beta-dehydrogenase-11-Antibody-Immunohistochemistry-Paraffin-NBP1-57081-img0004.jpg)
![Immunohistochemistry-Paraffin: hydroxysteroid (17-beta) dehydrogenase 11 Antibody [NBP1-57081] - Monkey vagina.](http://images.novusbio.com/fullsize/hydroxysteroid-17-beta-dehydrogenase-11-Antibody-Immunohistochemistry-Paraffin-NBP1-57081-img0003.jpg)
![Western Blot: MRP2 Antibody [NBP3-38537] - Western blot analysis of various lysates using MRP2 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: 90s.](http://images.novusbio.com/fullsize/nbp3-38537_rabbit-mrp2-pab-101220241136085.jpg "Western Blot: MRP2 Antibody [NBP3-38537] - Western blot analysis of various lysates using MRP2 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: 90s.")
![Western Blot: MRP2 Antibody [NBP3-38537] - Western blot analysis of various lysates using MRP2 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: 30s.](http://images.novusbio.com/fullsize/nbp3-38537_rabbit-mrp2-pab-1012202411381275.jpg)
![Western Blot: GCLC Antibody (0X1H3) [NBP3-16422] - Analysis of extracts of Rat kidney, using GCLC Rabbit mAb (NBP3-16422) 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: 3min.](http://images.novusbio.com/fullsize/GCLC-Antibody-0X1H3-Western-Blot-NBP3-16422-img0002.jpg "Western Blot: GCLC Antibody (0X1H3) [NBP3-16422] - Analysis of extracts of Rat kidney, using GCLC Rabbit mAb (NBP3-16422) 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: 3min.")
![Immunohistochemistry-Paraffin: GCLC Antibody (0X1H3) [NBP3-16422] - Rat kidney using GCLC Rabbit mAb (NBP3-16422) 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/GCLC-Antibody-0X1H3-Immunohistochemistry-Paraffin-NBP3-16422-img0001.jpg)
![Western Blot: GCLC Antibody (0X1H3) [NBP3-16422] - Analysis of extracts of various cell lines, using GCLC Rabbit mAb (NBP3-16422) 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 Enhanced Kit. Exposure time: 3min.](http://images.novusbio.com/fullsize/GCLC-Antibody-0X1H3-Western-Blot-NBP3-16422-img0003.jpg)
![Western Blot: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Western blot analysis of Cytochrome P450 1A2 on HepG2 cell lysates with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 58 kDa Observed band size: 50 kDa Exposure time: 2 minutes; 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 (NBP3-32241) 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/nbp3-32241_rabbit-cytochrome-p450-1a2-mab-je39-22-278202415295537.jpg "Western Blot: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Western blot analysis of Cytochrome P450 1A2 on HepG2 cell lysates with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 58 kDa Observed band size: 50 kDa Exposure time: 2 minutes; 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 (NBP3-32241) 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.")
![Immunocytochemistry/ Immunofluorescence: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Immunocytochemistry analysis of HepG2 cells labeling Cytochrome P450 1A2 with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/250 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-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/250 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/nbp3-32241_rabbit-cytochrome-p450-1a2-mab-je39-22-2920241192349.jpg)
![Flow Cytometry: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Flow cytometric analysis of HepG2 cells labeling Cytochrome P450 1A2. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32241, 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/nbp3-32241_rabbit-cytochrome-p450-1a2-mab-je39-22-39202488467.jpg)
![Western Blot: Pyruvate Carboxylase Antibody (JE40-24) [NBP3-32721] - Western blot analysis of Pyruvate Carboxylase on different lysates with Rabbit anti-Pyruvate Carboxylase antibody (NBP3-32721) at 1/1,000 dilution. Lane 1: Mouse liver tissue lysate Lane 2: Rat liver tissue lysate Lysates/proteins at 40 ug/Lane. Predicted band size: 130 kDa Observed band size: 130 kDa Exposure time: 1 minutes; 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 (NBP3-32721) 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/nbp3-32721_rabbit-pyruvate-carboxylase-mab-je40-24-278202416331212.jpg "Western Blot: Pyruvate Carboxylase Antibody (JE40-24) [NBP3-32721] - Western blot analysis of Pyruvate Carboxylase on different lysates with Rabbit anti-Pyruvate Carboxylase antibody (NBP3-32721) at 1/1,000 dilution. Lane 1: Mouse liver tissue lysate Lane 2: Rat liver tissue lysate Lysates/proteins at 40 ug/Lane. Predicted band size: 130 kDa Observed band size: 130 kDa Exposure time: 1 minutes; 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 (NBP3-32721) 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: Pyruvate Carboxylase Antibody (JE40-24) [NBP3-32721] - Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-Pyruvate Carboxylase antibody (NBP3-32721) 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 (NBP3-32721) 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/nbp3-32721_rabbit-pyruvate-carboxylase-mab-je40-24-2982024142096.jpg)