| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54319-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB110-55293SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26636-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-31909-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-25266 | |||
| Azide and BSA Free | NBP2-25266SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26590-50ul | |||
![Western Blot: PGC-1 beta Antibody [NBP1-28722] - Samples: Whole cell lysate (5, 15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-PGC-1beta antibody NBP1-28722 used for WB at 0.4 ug/ml (A) and 1 ug/ml (B) and used for IP at 10 ug/mg lysate. PGC-1beta was also immunoprecipitated by rabbit anti-PGC-1beta antibody NBP1-28721, which recognizes an upstream epitope. Detection: Chemiluminescence with exposure times of 30 seconds (A and B).](http://images.novusbio.com/fullsize/PGC-1-beta-Antibody-Western-Blot-NBP1-28722-img0001.jpg "<b>Independent Antibodies Validation and Biological Strategies Validation.</b>Western Blot: PGC-1 beta Antibody [NBP1-28722] - Samples: Whole cell lysate (5, 15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-PGC-1beta antibody NBP1-28722 used for WB at 0.4 ug/ml (A) and 1 ug/ml (B) and used for IP at 10 ug/mg lysate. PGC-1beta was also immunoprecipitated by rabbit anti-PGC-1beta antibody NBP1-28721, which recognizes an upstream epitope. Detection: Chemiluminescence with exposure times of 30 seconds (A and B).")
![<b>Independent Antibodies Validation and Biological Strategies Validation.</b>Western Blot: PGC-1 beta Antibody [NBP1-28722] - Whole cell lysate (50 ug) from HeLa, HEK293T, and MCF-7 cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-PGC-1beta antibody used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/antibody/nbp1-28722_rabbit-polyclonal-pgc-1-beta-antibody-western-blot-286202382436.jpg)
![Western Blot: Adiponectin/Acrp30 Antibody (ADPN/1370) [NBP2-47652] - Western blot Analysis of human Kidney lysate using Adiponectin/Acrp30 Antibody (ADPN/1370).](http://images.novusbio.com/fullsize/Adiponectin-Acrp30-Antibody-ADPN-1370-Western-Blot-NBP2-47652-img0004.jpg "Western Blot: Adiponectin/Acrp30 Antibody (ADPN/1370) [NBP2-47652] - Western blot Analysis of human Kidney lysate using Adiponectin/Acrp30 Antibody (ADPN/1370).")
![Immunohistochemistry-Paraffin: Adiponectin/Acrp30 Antibody (ADPN/1370) [NBP2-47652] - Formalin-fixed, paraffin-embedded human Kidney stained with Adiponectin Monoclonal Antibody (ADPN/1370).](http://images.novusbio.com/fullsize/Adiponectin-Acrp30-Antibody-ADPN-1370-Immunohistochemistry-Paraffin-NBP2-47652-img0001.jpg)
![Protein Array: Adiponectin/Acrp30 Antibody (ADPN/1370) [NBP2-47652] - Analysis of Protein Array containing more than 19,000 full-length human proteins using Adiponectin/Acrp30 Antibody (ADPN/1370). Z- and S- Score: The Z-score represents the strength of a signal that a monoclonal antibody (MAb) (in combination with a fluorescently-tagged anti-IgG secondary antibody) produces when binding to a particular protein on the HuProt(TM) array. Z-scores are described in units of standard deviations (SD's) above the mean value of all signals generated on that array. If targets on HuProt(TM) are arranged in descending order of the Z-score, the S-score is the difference (also in units of SD's) between the Z-score. S-score therefore represents the relative target specificity of a MAb to its intended target. A MAb is considered to specific to its intended target, if the MAb has an S-score of at least 2.5.](http://images.novusbio.com/fullsize/Adiponectin-Acrp30-Antibody-ADPN-1370-Protein-Array-NBP2-47652-img0003.jpg)
![Western Blot: GPIHBP1 Antibody [NB110-55293] - Detection of HDLBP in CHO transfected lysate using NB110-55293. Lane 1: empty vector Lane 2: HDLBP transfected lysate](http://images.novusbio.com/fullsize/GPIHBP1-Antibody-Western-Blot-NB110-55293-img0002.jpg "Western Blot: GPIHBP1 Antibody [NB110-55293] - Detection of HDLBP in CHO transfected lysate using NB110-55293. Lane 1: empty vector Lane 2: HDLBP transfected lysate")
![Immunohistochemistry: Aromatase Antibody (1H1) [NBP3-26636] - NBP3-26636 diluted at 1:300 and staining in paraffin-embedded human placenta tissue performed on a Leica BondTM system. 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.Secondary antibody only control: uses 1% BSA instead of primary antibody](http://images.novusbio.com/fullsize/nbp3-26636_rabbit-aromatase-mab-1h1-2612025101148.jpg "Immunohistochemistry: Aromatase Antibody (1H1) [NBP3-26636] - NBP3-26636 diluted at 1:300 and staining in paraffin-embedded human placenta tissue performed on a Leica BondTM system. 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.Secondary antibody only control: uses 1% BSA instead of primary antibody")
![Immunocytochemistry/Immunofluorescence: Aromatase Antibody (1H1) [NBP3-26636] - Staining of Hela cell with NBP3-26636 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26636_rabbit-aromatase-mab-1h1-2612025101147.jpg)
![Western Blot: Aromatase Antibody (1H1) [NBP3-26636] - Positive WB detected in: 293 whole cell lysate (20µg), K562 whole cell lysate (20µg), Hela whole cell lysate (20µg), MCF-7 whole cell lysate (20µg), PC-3 whole cell lysate (20µg)All lanes: CYP19A1 antibody at 1:1000SecondaryGoat polyclonal to rabbit IgG at 1/50000 dilutionPredicted band size: 58 kDaObserved band size: 58 kDaExposure time：120s](http://images.novusbio.com/fullsize/nbp3-26636_rabbit-aromatase-mab-1h1-2612025101143.jpg)
![Immunocytochemistry/Immunofluorescence: Aromatase Antibody (1H1) [NBP3-26636] - Staining of Hela cell with 5% goat serum, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26636_rabbit-aromatase-mab-1h1-26120251011416.jpg)
![Western Blot: PKLR Antibody [NBP2-20027] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PKLR Antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/PKLR-Antibody-Western-Blot-NBP2-20027-img0004.jpg "Western Blot: PKLR Antibody [NBP2-20027] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PKLR Antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: PKLR Antibody [NBP2-20027] - Human breast cancer, using Pyruvate Kinase (liver/RBC) antibody at 1:250 dilution.Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/PKLR-Antibody-Immunohistochemistry-Paraffin-NBP2-20027-img0001.jpg)
![Western Blot: PKLR Antibody [NBP2-20027] - A. 20 ug Rat liver lysate/extract 7.5% SDS-PAGE Pyruvate Kinase (liver/RBC) antibody dilution: 1:10000](http://images.novusbio.com/fullsize/PKLR-Antibody-Western-Blot-NBP2-20027-img0003.jpg)
![Western Blot: dUTPase Antibody [NB100-56624] - Detection of DUT-N in HeLa cell lysate using this antibody at a dilution of 1:1000.](http://images.novusbio.com/fullsize/dUTPase-Antibody-Western-Blot-NB100-56624-img0002.jpg "Western Blot: dUTPase Antibody [NB100-56624] - Detection of DUT-N in HeLa cell lysate using this antibody at a dilution of 1:1000.")
![Immunohistochemistry-Paraffin: SRD5A1 Antibody [NBP2-31909] - Staining of human prostate shows strong cytoplasmic positivity in glandular cells.](http://images.novusbio.com/fullsize/SRD5A1-Antibody-Immunohistochemistry-Paraffin-NBP2-31909-img0005.jpg "Immunohistochemistry-Paraffin: SRD5A1 Antibody [NBP2-31909] - Staining of human prostate shows strong cytoplasmic positivity in glandular cells.")
![Western Blot: Noxa Antibody (69N15C9) [NBP2-25251] - Western blot analysis of mouse A) Noxa recombinant protein, B) thymus and C) ovary using Noxa antibody at 1 ug/mL, 5 ug/mL and 5 ug/mL, respectively.](http://images.novusbio.com/fullsize/Noxa-Antibody-69N15C9-Western-Blot-NBP2-25251-img0001.jpg "Western Blot: Noxa Antibody (69N15C9) [NBP2-25251] - Western blot analysis of mouse A) Noxa recombinant protein, B) thymus and C) ovary using Noxa antibody at 1 ug/mL, 5 ug/mL and 5 ug/mL, respectively.")
![Western Blot: PON1 Antibody [NBP2-19893] - . Human tissue extracts (30 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with PON1 antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/PON1-Antibody-Western-Blot-NBP2-19893-img0002.jpg "Western Blot: PON1 Antibody [NBP2-19893] - . Human tissue extracts (30 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with PON1 antibody diluted at 1:1000.")
![Immunohistochemistry-Paraffin: PON1 Antibody [NBP2-19893] - Analysis of mouse liver. PON1 antibody diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/PON1-Antibody-Immunohistochemistry-Paraffin-NBP2-19893-img0001.jpg)
![Immunohistochemistry: FADS1 Antibody (7A10) [NBP3-26590] - Image of FADS1 Antibody (7A10) diluted at 1:100 and staining in paraffin-embedded human endometrial cancer 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-262202414471574.jpg "Immunohistochemistry: FADS1 Antibody (7A10) [NBP3-26590] - Image of FADS1 Antibody (7A10) diluted at 1:100 and staining in paraffin-embedded human endometrial cancer 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Western Blot: FADS1 Antibody (7A10) [NBP3-26590] - Positive Western Blot detected in: MCF-7 whole cell lysate, A549 whole cell lysate, Hela whole cell lysate. All lanes: FADS1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 52, 43 kDa Observed band size: 55 kDa](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-28220241152510.jpg)
![Immunocytochemistry/Immunofluorescence: FADS1 Antibody (7A10) [NBP3-26590] - Staining of HepG2 cell with FADS1 Antibody (7A10) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 565-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26590_rabbit-fads1-mab-7a10-282202412475112.jpg)
![Flow Cytometry: FADS1 Antibody (7A10) [NBP3-26590] - Overlay Peak curve showing HepG2 cells stained with FADS1 Antibody (7A10) (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min 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/nbp3-26590_rabbit-fads1-mab-7a10-282202414183689.jpg)
![Western Blot: BMAL1 Antibody [NBP2-15599] - Analysis of ARNTL expression in transfected 293T cell line by ARNTL polyclonal antibody. A: Non-transfected lysate. B: ARNTL transfected lysate. 7. 5% SDS PAGE gel, diluted at 1:500.](http://images.novusbio.com/fullsize/BMAL1-Antibody-Western-Blot-NBP2-15599-img0005.jpg "Western Blot: BMAL1 Antibody [NBP2-15599] - Analysis of ARNTL expression in transfected 293T cell line by ARNTL polyclonal antibody. A: Non-transfected lysate. B: ARNTL transfected lysate. 7. 5% SDS PAGE gel, diluted at 1:500.")
![Immunocytochemistry/Immunofluorescence: BMAL1 Antibody [NBP2-15599] - A375 cells. Green: MOP3 protein stained by MOP3 antibody [N1N3] Blue: Hoechst 33342 staining.](http://images.novusbio.com/fullsize/BMAL1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-15599-img0003.jpg)
![Western Blot: BMAL1 Antibody [NBP2-15599] - Sample (50 ug of whole cell lysate) A: Mouse Brain, 7. 5% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/BMAL1-Antibody-Western-Blot-NBP2-15599-img0004.jpg)
![<b>Biological Strategies Validation. </b>Western Blot: BMAL1 Antibody [NBP2-15599] - Treated 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membranes were blotted with BMAL1 antibody [N1N3] and PER2 antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-15599_rabbit-polyclonal-bmal1-antibody-1610202419405778.jpg)