| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-99339-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90461-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26589-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26349-50ul | |||
![Immunohistochemistry-Paraffin: ACSL1 Antibody [NBP2-99339] - Immunochemical staining of human ACSL1 in human kidney with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/ACSL1-Antibody-Immunohistochemistry-Paraffin-NBP2-99339-img0002.jpg "Immunohistochemistry-Paraffin: ACSL1 Antibody [NBP2-99339] - Immunochemical staining of human ACSL1 in human kidney with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: ACSL1 Antibody [NBP2-99339] - Immunochemical staining of human ACSL1 in human hepatoma with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/ACSL1-Antibody-Immunohistochemistry-Paraffin-NBP2-99339-img0001.jpg)
![Immunohistochemistry: Monoglyceride Lipase Antibody [NBP3-30968] - Immunohistochemical staining of human adipose tissue using MGL antibody (Cat. No. NBP3-30968). Antibody used at 2 ug/ml. 40x magnification.](http://images.novusbio.com/fullsize/nbp3-30968_rabbit-monoglyceride-lipase-pab-811202420592166.jpg "Immunohistochemistry: Monoglyceride Lipase Antibody [NBP3-30968] - Immunohistochemical staining of human adipose tissue using MGL antibody (Cat. No. NBP3-30968). Antibody used at 2 ug/ml. 40x magnification.")
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody (JE63-95) [NBP3-33135] - Western blot analysis of Acetyl-CoA Carboxylase alpha/ACACA on different lysates with Rabbit anti-Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-33135) at 1/2,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes cell lysate Lane 3: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes then treated with pp for 1 hour cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 265 kDa Observed band size: 265 kDa Exposure time: 1 minutes 14 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 (NBP3-33135) at 1/2,000 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/nbp3-33135_rabbit-acetyl-coa-carboxylase-alpha-acaca-p-ser79-mab-28820241423319.jpg "Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody (JE63-95) [NBP3-33135] - Western blot analysis of Acetyl-CoA Carboxylase alpha/ACACA on different lysates with Rabbit anti-Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-33135) at 1/2,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes cell lysate Lane 3: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes then treated with pp for 1 hour cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 265 kDa Observed band size: 265 kDa Exposure time: 1 minutes 14 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 (NBP3-33135) at 1/2,000 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.")
![Flow Cytometry: RBP4/Retinol-Binding Protein 4 Antibody (008) [NBP2-90461] - Flow cytometric analysis of Rat CD59 expression on SD rat bone marrow cells. Cells were stained with purified anti-Rat CD59, 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/RBP4-Retinol-Binding-Protein-4-Antibody-008-Flow-Cytometry-NBP2-90461-img0001.jpg "Flow Cytometry: RBP4/Retinol-Binding Protein 4 Antibody (008) [NBP2-90461] - Flow cytometric analysis of Rat CD59 expression on SD rat bone marrow cells. Cells were stained with purified anti-Rat CD59, 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.")
![Immunocytochemistry/ Immunofluorescence: RBP4/Retinol-Binding Protein 4 Antibody (008) [NBP2-90461] - Immunofluorescence staining of RBP4/Retinol-Binding Protein 4 in mouse splenocytes. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90461 (1:60) at 37 1 hour. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green).](http://images.novusbio.com/fullsize/nbp2-90461_rabbit-monoclonal-rbp4-retinol-binding-protein-4-antibody-008-235202512205528.png)
![Western Blot: Aldo-keto Reductase 1C3/AKR1C3 Antibody (JE36-28) [NBP3-32015] - Western blot analysis of Aldo-keto Reductase 1C3/AKR1C3 on different lysates with Rabbit anti-Aldo-keto Reductase 1C3/AKR1C3 antibody (NBP3-32015) at 1/1,000 dilution. Lane 1: A549 cell lysate (20 ug/Lane) Lane 2: HepG2 cell lysate (20 ug/Lane) Lane 3: K-562 cell lysate (20 ug/Lane) Lane 4: Human kidney tissue lysate (40 ug/Lane) Lane 5: Mouse kidney tissue lysate (40 ug/Lane) Lane 6: Rat kidney tissue lysate (40 ug/Lane) Predicted band size: 37 kDa Observed band size: 35 kDa Exposure time: 20 seconds; 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 (NBP3-32015) 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/nbp3-32015_rabbit-aldo-keto-reductase-1c3-akr1c3-mab-je36-28-27820241514172.jpg "Western Blot: Aldo-keto Reductase 1C3/AKR1C3 Antibody (JE36-28) [NBP3-32015] - Western blot analysis of Aldo-keto Reductase 1C3/AKR1C3 on different lysates with Rabbit anti-Aldo-keto Reductase 1C3/AKR1C3 antibody (NBP3-32015) at 1/1,000 dilution. Lane 1: A549 cell lysate (20 ug/Lane) Lane 2: HepG2 cell lysate (20 ug/Lane) Lane 3: K-562 cell lysate (20 ug/Lane) Lane 4: Human kidney tissue lysate (40 ug/Lane) Lane 5: Mouse kidney tissue lysate (40 ug/Lane) Lane 6: Rat kidney tissue lysate (40 ug/Lane) Predicted band size: 37 kDa Observed band size: 35 kDa Exposure time: 20 seconds; 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 (NBP3-32015) 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.")
![Immunocytochemistry/Immunofluorescence: Aldo-keto Reductase 1C3/AKR1C3 Antibody (4D12) [NBP3-15212] - Immunofluorescence staining of Hela Cells with at Aldo-keto Reductase 1C3/AKR1C3 antibody 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/Aldo-keto-Reductase-1C3-AKR1C3-Antibody-4D12-Immunocytochemistry-Immunofluorescence-NBP3-15212-img0002.jpg "Immunocytochemistry/Immunofluorescence: Aldo-keto Reductase 1C3/AKR1C3 Antibody (4D12) [NBP3-15212] - Immunofluorescence staining of Hela Cells with at Aldo-keto Reductase 1C3/AKR1C3 antibody 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: Aldo-keto Reductase 1C3/AKR1C3 Antibody (4D12) [NBP3-15212] - Overlay histogram showing A549 cells stained with Aldo-keto Reductase 1C3/AKR1C3 antibody (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followedby the antibody (1ug/1*106cells) for 1 h at 4C.The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min at 4C. Control antibody (green line) was Rabbit IgG (1ug/1*106cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/Aldo-keto-Reductase-1C3-AKR1C3-Antibody-4D12-Flow-Cytometry-NBP3-15212-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: Fatty Acid Synthase/FASN Antibody (2A5) [NBP3-26589] - Staining of Hela Cells with Fatty Acid Synthase/FASN Antibody (2A5) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26589_rabbit-fatty-acid-synthase-fasn-mab-2a5-282202412493622.jpg "Immunocytochemistry/Immunofluorescence: Fatty Acid Synthase/FASN Antibody (2A5) [NBP3-26589] - Staining of Hela Cells with Fatty Acid Synthase/FASN Antibody (2A5) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: Fatty Acid Synthase/FASN Antibody (2A5) [NBP3-26589] - Overlay histogram showing A549 cells stained with Fatty Acid Synthase/FASN Antibody (2A5) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min at 4C. Control antibody (green line) was Rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26589_rabbit-fatty-acid-synthase-fasn-mab-2a5-282202414183634.jpg)
![Immunohistochemistry: RBP4/Retinol-Binding Protein 4 Antibody (9G7) [NBP3-26349] - Image of RBP4/Retinol-Binding Protein 4 Antibody (9G7) diluted at 1:100 and staining in paraffin-embedded human liver tissue performed. 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 30min 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/nbp3-26349_rabbit-rbp4-retinol-binding-protein-4-mab-9g7-26220241522410.jpg "Immunohistochemistry: RBP4/Retinol-Binding Protein 4 Antibody (9G7) [NBP3-26349] - Image of RBP4/Retinol-Binding Protein 4 Antibody (9G7) diluted at 1:100 and staining in paraffin-embedded human liver tissue performed. 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 30min 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.")
![Immunohistochemistry: RBP4/Retinol-Binding Protein 4 Antibody (9G7) [NBP3-26349] - Image of RBP4/Retinol-Binding Protein 4 Antibody (9G7) diluted at 1:100 and staining in paraffin-embedded human liver tissue performed. 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 30min 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/nbp3-26349_rabbit-rbp4-retinol-binding-protein-4-mab-9g7-27220248504611.jpg)