| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-05407-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-38617-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-38479-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-92133-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21934-50ul | |||
![Western Blot: SUR1 Antibody [NBP1-59778] - 293T cell lysate, Antibody Titration: 0.2-1 ug/ml](http://images.novusbio.com/fullsize/SUR1-Antibody-Western-Blot-NBP1-59778-img0005.jpg "Western Blot: SUR1 Antibody [NBP1-59778] - 293T cell lysate, Antibody Titration: 0.2-1 ug/ml")
![Immunohistochemistry-Paraffin: SUR1 Antibody [NBP1-59778] - Human small intestine tissue at an antibody concentration of 4-8ug/ml.](http://images.novusbio.com/fullsize/SUR1-Antibody-Immunohistochemistry-Paraffin-NBP1-59778-img0004.jpg)
![Western Blot: Kir6.2 Antibody [NB100-93410] - Analysis of Kir6.2 in Human Muscle lysate (35ug protein in RIPA buffer) using NB100-93410 at 0.1ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Kir6.2-Antibody-Western-Blot-NB100-93410-img0002.jpg "Western Blot: Kir6.2 Antibody [NB100-93410] - Analysis of Kir6.2 in Human Muscle lysate (35ug protein in RIPA buffer) using NB100-93410 at 0.1ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: Kir6.2 Antibody [NB100-93410] - (3.8ug/ml) staining of paraffin embedded Human Pancreas. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](http://images.novusbio.com/fullsize/Kir6.2-Antibody-Immunohistochemistry-Paraffin-NB100-93410-img0001.jpg)
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [ac Ser79] Antibody [NBP3-05407] - Western blot analysis of extracts of 293T cells, using Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-05407) at 1:1000 dilution.293T cells were treated by CIP(20uL/400ul) at 37C for 1 hour. 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/Acetyl-CoA-Carboxylase-alpha-ACACA-[ac-Ser79]-Antibody-Western-Blot-NBP3-05407-img0001.jpg "Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [ac Ser79] Antibody [NBP3-05407] - Western blot analysis of extracts of 293T cells, using Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-05407) at 1:1000 dilution.293T cells were treated by CIP(20uL/400ul) at 37C for 1 hour. 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.")
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody - Azide and BSA Free [Acetyl-CoA Carboxylase alpha/ACACA] - Western blot analysis of lysates from RAW264.7 cells, using Acetyl-CoA Carboxylase alpha/ACACA Rabbit pAb at 1:700 dilution. RAW264. 7 cells were treated by lambda-PP mixed solution (1ul) at 30C for 30 minutes.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 Enhanced Kit .Exposure time: 90s.](http://images.novusbio.com/fullsize/nbp3-05407_rabbit-polyclonal-acetyl-coa-carboxylase-alpha-acaca-p-ser79-antibody-5220251639637.jpg)
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody - Azide and BSA Free [Acetyl-CoA Carboxylase alpha/ACACA] - Western blot analysis of lysates from A-431 cells, using Acetyl-CoA Carboxylase alpha/ACACA Rabbit pAb at 1:700 dilution. A-431 cells were treated by lambda-PP mixed solution (1ul) at 30C for 30 minutes.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 Enhanced Kit .Exposure time: 90s.](http://images.novusbio.com/fullsize/nbp3-05407_rabbit-polyclonal-acetyl-coa-carboxylase-alpha-acaca-p-ser79-antibody-5220251626462.jpg)
![Western Blot: TIMM8A Antibody [NBP3-38617] - Western blot analysis of lysates from U-87MG cells, using TIMM8A Rabbit pAb at 1:600 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 Enhanced Kit.Exposure time: 90s.](http://images.novusbio.com/fullsize/nbp3-38617_rabbit-timm8a-pab-1012202411433451.jpg "Western Blot: TIMM8A Antibody [NBP3-38617] - Western blot analysis of lysates from U-87MG cells, using TIMM8A Rabbit pAb at 1:600 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 Enhanced Kit.Exposure time: 90s.")
![Immunocytochemistry/ Immunofluorescence: TIMM8A Antibody [NBP3-38617] - Immunofluorescence analysis of C6 cells using TIMM8A Rabbit pAb at dilution of 1:100 (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/nbp3-38617_rabbit-timm8a-pab-1012202411364676.jpg)
![Western Blot: ALDH9A1 Antibody [NBP3-38479] - Western blot analysis of various lysates, using ALDH9A1 Rabbit pAb at 1:1500 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: 60s.](http://images.novusbio.com/fullsize/nbp3-38479_rabbit-aldh9a1-pab-10122024120638.jpg "Western Blot: ALDH9A1 Antibody [NBP3-38479] - Western blot analysis of various lysates, using ALDH9A1 Rabbit pAb at 1:1500 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: 60s.")
![Western Blot: ALDH9A1 Antibody [NBP3-38479] - Western Blot analysis of lysates from U-251 MG cells using ALDH9A1 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 60s.](http://images.novusbio.com/fullsize/nbp3-38479_rabbit-aldh9a1-pab-3112025177030.jpg)
![Immunocytochemistry/Immunofluorescence: CPT1C Antibody [NBP2-92133] - Immunofluorescence analysis of L929 cells using CPT1C antibody (NBP2-92133) at dilution of 1:100. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/CPT1C-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-92133-img0002.jpg "Immunocytochemistry/Immunofluorescence: CPT1C Antibody [NBP2-92133] - Immunofluorescence analysis of L929 cells using CPT1C antibody (NBP2-92133) at dilution of 1:100. Blue: DAPI for nuclear staining.")
![Western Blot: CPT1C Antibody [NBP2-92133] - analysis of various lysates, using CPT1C Rabbit pAb at 1:7000 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: 180s.](http://images.novusbio.com/fullsize/nbp2-92133_rabbit-polyclonal-cpt1c-antibody-western-blot-222202413728..jpg)
![Western Blot: PGC1 alpha Antibody (1G8) [NBP2-37562] - Analysis using PGC1 alpha Antibody (1G8) against HEK293 (1) and PGC-1alpha-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/PGC1-alpha-Antibody-1G8-Western-Blot-NBP2-37562-img0003.jpg "Western Blot: PGC1 alpha Antibody (1G8) [NBP2-37562] - Analysis using PGC1 alpha Antibody (1G8) against HEK293 (1) and PGC-1alpha-hIgGFc transfected HEK293 (2) cell lysate.")
![Western Blot: PGC1 alpha Antibody (1G8) [NBP2-37562] - Analysis using PGC1 alpha Antibody (1G8) against human PGC-1alpha (AA: 570-798) recombinant protein. Expected molecular weight is 70 KDa.](http://images.novusbio.com/fullsize/PGC1-alpha-Antibody-1G8-Western-Blot-NBP2-37562-img0002.jpg)
![ELISA: PGC1 alpha Antibody (1G8) [NBP2-37562] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/PGC1-alpha-Antibody-1G8-ELISA-NBP2-37562-img0001.jpg)
![Western Blot: Aldehyde Dehydrogenase 1-A1/ALDH1A1 Antibody (8F1-R) [NBP3-32019] - Western blot analysis of Aldehyde Dehydrogenase 1-A1/ALDH1A1 on different lysates with Mouse anti-Aldehyde Dehydrogenase 1-A1/ALDH1A1 antibody (NBP3-32019) at 1/1,000 dilution. Lane 1: A549 cell lysate (20 ug/Lane) Lane 2: HT-29 cell lysate (20 ug/Lane) Lane 3: HepG2 cell lysate (20 ug/Lane) Lane 4: K-562 cell lysate (20 ug/Lane) Lane 5: Human liver tissue lysate (40 ug/Lane) Lane 6: Human lung tissue lysate (40 ug/Lane) Predicted band size: 55 kDa Observed band size: 50 kDa Exposure time: 1 minute; 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 (NBP3-32019) 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 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32019_mouse-aldehyde-dehydrogenase-1-a1-aldh1a1-mab-8f1-r-278202415141717.jpg "Western Blot: Aldehyde Dehydrogenase 1-A1/ALDH1A1 Antibody (8F1-R) [NBP3-32019] - Western blot analysis of Aldehyde Dehydrogenase 1-A1/ALDH1A1 on different lysates with Mouse anti-Aldehyde Dehydrogenase 1-A1/ALDH1A1 antibody (NBP3-32019) at 1/1,000 dilution. Lane 1: A549 cell lysate (20 ug/Lane) Lane 2: HT-29 cell lysate (20 ug/Lane) Lane 3: HepG2 cell lysate (20 ug/Lane) Lane 4: K-562 cell lysate (20 ug/Lane) Lane 5: Human liver tissue lysate (40 ug/Lane) Lane 6: Human lung tissue lysate (40 ug/Lane) Predicted band size: 55 kDa Observed band size: 50 kDa Exposure time: 1 minute; 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 (NBP3-32019) 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 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: Aldehyde Dehydrogenase 1-A1/ALDH1A1 Antibody (8F1-R) [NBP3-32019] - Immunocytochemistry analysis of A549 cells labeling Aldehyde Dehydrogenase 1-A1/ALDH1A1 with Mouse anti-Aldehyde Dehydrogenase 1-A1/ALDH1A1 antibody (NBP3-32019) 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-Aldehyde Dehydrogenase 1-A1/ALDH1A1 antibody (NBP3-32019) 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/nbp3-32019_mouse-aldehyde-dehydrogenase-1-a1-aldh1a1-mab-8f1-r-29202410234298.jpg)
![Flow Cytometry: Aldehyde Dehydrogenase 1-A1/ALDH1A1 Antibody (8F1-R) [NBP3-32019] - Flow cytometric analysis of A549 cells labeling Aldehyde Dehydrogenase 1-A1/ALDH1A1. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32019, 1μg/mL) (red) compared with Mouse IgG1 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-Mouse 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/nbp3-32019_mouse-aldehyde-dehydrogenase-1-a1-aldh1a1-mab-8f1-r-29202416453266.jpg)
![Western Blot: PMP70 Antibody (JE39-00) [NBP3-32833] - Western blot analysis of PMP70 on different lysates with Rabbit anti-PMP70 antibody (NBP3-32833) at 1/1,000 dilution. Lane 1: Mouse liver tissue lysate Lane 2: Mouse kidney tissue lysate Lane 3: Rat liver tissue lysate Lysates/proteins at 40 ug/Lane. Predicted band size: 76 kDa Observed band size: 70 kDa Exposure time: 3 minutes 10 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 (NBP3-32833) 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/nbp3-32833_rabbit-pmp70-mab-je39-00-288202412461622.jpg "Western Blot: PMP70 Antibody (JE39-00) [NBP3-32833] - Western blot analysis of PMP70 on different lysates with Rabbit anti-PMP70 antibody (NBP3-32833) at 1/1,000 dilution. Lane 1: Mouse liver tissue lysate Lane 2: Mouse kidney tissue lysate Lane 3: Rat liver tissue lysate Lysates/proteins at 40 ug/Lane. Predicted band size: 76 kDa Observed band size: 70 kDa Exposure time: 3 minutes 10 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 (NBP3-32833) 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: PMP70 Antibody (JE39-00) [NBP3-32833] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-PMP70 antibody (NBP3-32833) 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 (NBP3-32833) 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/nbp3-32833_rabbit-pmp70-mab-je39-00-298202414304140.jpg)
![Western Blot: FDFT1 Antibody (10H12) [NBP3-15199] - Positive WB detected in: THP-1 whole cell lysate, K562 whole cell lysate. All lanes: FDFT1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49, 41, 39, 36, 44 KDa. Observed band size: 50 KDa.](http://images.novusbio.com/fullsize/FDFT1-Antibody-10H12-Western-Blot-NBP3-15199-img0003.jpg "Western Blot: FDFT1 Antibody (10H12) [NBP3-15199] - Positive WB detected in: THP-1 whole cell lysate, K562 whole cell lysate. All lanes: FDFT1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49, 41, 39, 36, 44 KDa. Observed band size: 50 KDa.")
![Immunohistochemistry: FDFT1 Antibody (10H12) [NBP3-15199] - IHC image of FDFT1 antibody diluted at 1:100 and staining in paraffin-embedded human lung cancer. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/FDFT1-Antibody-10H12-Immunohistochemistry-NBP3-15199-img0002.jpg)
![Immunohistochemistry: FDFT1 Antibody (10H12) [NBP3-15199] - IHC image of FDFT1 antibody diluted at 1:100 and staining in paraffin-embedded human testis tissue. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/FDFT1-Antibody-10H12-Immunohistochemistry-NBP3-15199-img0001.jpg)
![Western Blot: FDFT1 Antibody (SR1832) [NBP3-21934] - Western blot analysis using NBP3-21934 in (1) HepG2 cell lysate; (2) RAW264.7 cell lysate.](http://images.novusbio.com/fullsize/nbp3-21934_rabbit-fdft1-mab-sr1832-5720231754815.jpg "Western Blot: FDFT1 Antibody (SR1832) [NBP3-21934] - Western blot analysis using NBP3-21934 in (1) HepG2 cell lysate; (2) RAW264.7 cell lysate.")