| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-93042-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-61887-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98781-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-14796-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26200-50ul | |||
![Western Blot: 14-3-3 zeta/beta Antibody (3J3J9) [NBP3-16769] - Western blot analysis of extracts of various cell lines, using 14-3-3 zeta/beta Rabbit mAb (NBP3-16769) 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: 1s.](http://images.novusbio.com/fullsize/14-3-3-zeta-beta-Antibody-3J3J9-Western-Blot-NBP3-16769-img0002.jpg "Western Blot: 14-3-3 zeta/beta Antibody (3J3J9) [NBP3-16769] - Western blot analysis of extracts of various cell lines, using 14-3-3 zeta/beta Rabbit mAb (NBP3-16769) 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: 1s.")
![Immunocytochemistry/ Immunofluorescence: 14-3-3 zeta/beta Antibody (3J3J9) [NBP3-16769] - Immunofluorescence analysis of NIH-3T3 cells using 14-3-3 zeta/beta Rabbit mAb at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-16769_rabbit-14-3-3-zeta-beta-mab-3j3j9-8220252010488.jpg)
![Western Blot: E2F6 Antibody (9I5M0) [NBP3-15400] - Western blot analysis of extracts of various cell lines, using E2F6 Rabbit mAb (NBP3-15400) 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: 90s.](http://images.novusbio.com/fullsize/E2F6-Antibody-9I5M0-Western-Blot-NBP3-15400-img0001.jpg "Western Blot: E2F6 Antibody (9I5M0) [NBP3-15400] - Western blot analysis of extracts of various cell lines, using E2F6 Rabbit mAb (NBP3-15400) 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: 90s.")
![Chromatin Immunoprecipitation: E2F6 Antibody (9I5M0) [NBP3-15400] - Chromatin immunoprecipitation analysis of extracts of 293T cells, using E2F6 antibody (NBP3-15400) and rabbit IgG.The amount of immunoprecipitated DNA was checked by quantitative PCR. Histogram was constructed by the ratios of the immunoprecipitated DNA to the input.](http://images.novusbio.com/fullsize/E2F6-Antibody-9I5M0-Chromatin-Immunoprecipitation-NBP3-15400-img0003.jpg)
![Immunoprecipitation: E2F6 Antibody (9I5M0) [NBP3-15400] - Immunoprecipitation analysis of 300ug extracts of 293T cells using 3ug E2F6 antibody (NBP3-15400). Western blot was performed from the immunoprecipitate using E2F6 antibody (NBP3-15400) at a dilition of 1:1000.](http://images.novusbio.com/fullsize/E2F6-Antibody-9I5M0-Immunoprecipitation-NBP3-15400-img0002.jpg)
![Western Blot: SETD8 Antibody [NBP2-93042] - Analysis of extracts of various cell lines, using SETD8 . Exposure time: 60s.](http://images.novusbio.com/fullsize/SETD8-Antibody-Western-Blot-NBP2-93042-img0002.jpg "Western Blot: SETD8 Antibody [NBP2-93042] - Analysis of extracts of various cell lines, using SETD8 . Exposure time: 60s.")
![Immunocytochemistry/Immunofluorescence: SETD8 Antibody [NBP2-93042] - Analysis of MCF-7 cells using SETD8 .](http://images.novusbio.com/fullsize/SETD8-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-93042-img0001.jpg)
![Western Blot: Apc1 Antibody (7G9C7) [NBP2-61887] - Analysis using ANAPC1 mAb against human ANAPC1 (AA: 12-155) recombinant protein. (Expected MW is 41.9 kDa)](http://images.novusbio.com/fullsize/Apc1-Antibody-7G9C7-Western-Blot-NBP2-61887-img0003.jpg "Western Blot: Apc1 Antibody (7G9C7) [NBP2-61887] - Analysis using ANAPC1 mAb against human ANAPC1 (AA: 12-155) recombinant protein. (Expected MW is 41.9 kDa)")
![Flow Cytometry: Apc1 Antibody (7G9C7) [NBP2-61887] - Analysis of MCF-7 cells using ANAPC1 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/Apc1-Antibody-7G9C7-Flow-Cytometry-NBP2-61887-img0002.jpg)
![Western Blot: Apc1 Antibody (7G9C7) [NBP2-61887] - Analysis using ANAPC1 mAb against HEK293 (1) and ANAPC1 (AA: 12-155)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/Apc1-Antibody-7G9C7-Western-Blot-NBP2-61887-img0004.jpg)
![ELISA: Apc1 Antibody (7G9C7) [NBP2-61887] - Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)](http://images.novusbio.com/fullsize/Apc1-Antibody-7G9C7-ELISA-NBP2-61887-img0001.jpg)
![Western Blot: HDAC7 Antibody [NB100-2146] - Cell line lysates were separated on SDS-PAGE and probed with 1:500 Rabbit Anti-Histone Deacetylase 7 (HDAC7) (KG-17). The antibody was developed using Goat Anti-Rabbit IgG-Peroxidase ) and a chemiluminescent substrate.Lanes:1. HeLa nuclear2. NIH-3T3](http://images.novusbio.com/fullsize/HDAC7-Antibody-Western-Blot-NB100-2146-img0002.jpg "Western Blot: HDAC7 Antibody [NB100-2146] - Cell line lysates were separated on SDS-PAGE and probed with 1:500 Rabbit Anti-Histone Deacetylase 7 (HDAC7) (KG-17). The antibody was developed using Goat Anti-Rabbit IgG-Peroxidase ) and a chemiluminescent substrate.Lanes:1. HeLa nuclear2. NIH-3T3")
![Immunoprecipitation: HDAC7 Antibody [NB100-2146] - Immunoprecipitation HDAC7 was immunoprecipitated from whole cell extract of human HEK 293T cells expressing HDAC7-FLAG using Rabbit Anti-HDAC7 (KG-17) antibody (NB100-2146). The IP samples were separated on SDS-PAGE and blotted with Rabbit Anti-FLAG antibody. The antibody was developed with Goat anti-Rabbit IgG, Peroxidase conjugate and chemiluminescent substrate. Lane 1: 1.8 ug Antibody immunoprecipitates HDAC7 from a RIPA extract of 180 ug of 293T cells expressing HDAC7-FLAG. Lane 2: negative control (extract without antibody).](http://images.novusbio.com/fullsize/HDAC7-Antibody-Immunoprecipitation-NB100-2146-img0001.jpg)
![Western Blot: NCAPH Antibody [NBP2-98781] - Lane A: K562 Whole Cell LysateLane B: HepG2 Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti- Rabbit IgG H&L (Dylight 800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:82 kDaObserved band size:110 kDa](http://images.novusbio.com/fullsize/NCAPH-Antibody-Western-Blot-NBP2-98781-img0001.jpg "Western Blot: NCAPH Antibody [NBP2-98781] - Lane A: K562 Whole Cell LysateLane B: HepG2 Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti- Rabbit IgG H&L (Dylight 800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:82 kDaObserved band size:110 kDa")
![Immunoprecipitation: NCAPH Antibody [NBP2-98781] - Lane A:0.5 mg K562 Whole Cell LysateLane B:0.5 mg HepG2 Whole Cell Lysate4 uL anti-NCAPH rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose.Primary antibody:Anti-NCAPH rabbit polyclonal antibody,at 1:100 dilution Secondary antibody:Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution Developed using the odssey technique.Performed under reducing conditions.Predicted band size: 83 kDaObserved band size: 110 kDa](http://images.novusbio.com/fullsize/NCAPH-Antibody-Immunoprecipitation-NBP2-98781-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: NCAPH Antibody [NBP2-98781] - Staining of NCAPH in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP2-98781 antibody (1:1000) at 4? overnight. Then cells were stained with the Alexa Fluor488-conjugated Goat Anti-rabbit IgG secondary antibody (green).Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-98781_rabbit-polyclonal-ncaph-antibody-23520251135415.png)
![Western Blot: Pit1 Antibody [NBP2-85477] - WB Suggested Anti-POU1F1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:12500. Positive Control: HepG2 cell lysate](http://images.novusbio.com/fullsize/Pit1-Antibody-Western-Blot-NBP2-85477-img0002.jpg "Western Blot: Pit1 Antibody [NBP2-85477] - WB Suggested Anti-POU1F1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:12500. Positive Control: HepG2 cell lysate")
![Immunohistochemistry-Paraffin: Pit1 Antibody [NBP2-85477] - Rabbit Anti-POU1F1 Antibody. Paraffin Embedded Tissue: Human pituitary. Observed staining: Nuclear. Primary Antibody Dilution: 1:600. Conditions: Primary antibody incubation at RT for 1 hour. Detection was done using HRP -polymer conjugated anti-rabbit secondary antibody by incubating for 30 minutes at RT. Chromogen: DAB. Counterstaining: Hematoxylin.](http://images.novusbio.com/fullsize/Pit1-Antibody-Immunohistochemistry-Paraffin-NBP2-85477-img0001.jpg)
![Western Blot: Pit1 Antibody [NBP2-85477] - Host: Rabbit. Target Name: POU1F1. Sample Tissue: Human HT1080 Whole Cell. Antibody Dilution: 1ug/ml](http://images.novusbio.com/fullsize/Pit1-Antibody-Western-Blot-NBP2-85477-img0003.jpg)
![Immunocytochemistry/ Immunofluorescence: SON Antibody - BSA Free [NBP3-30739] - Immunofluorescence staining of SON in U251MG cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP3-30739 (dilution ratio 1:100) at 4 overnight. Then cells were stained with the Alexa Fluor488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus.](http://images.novusbio.com/fullsize/nbp3-30739_rabbit-son-pab-235202511545686.png "Immunocytochemistry/ Immunofluorescence: SON Antibody - BSA Free [NBP3-30739] - Immunofluorescence staining of SON in U251MG cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP3-30739 (dilution ratio 1:100) at 4 overnight. Then cells were stained with the Alexa Fluor488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus.")
![Immunohistochemistry-Paraffin: SON Antibody - BSA Free [NBP3-30739] - Immunochemical staining of human SON in human prostate with NBP3-30739 at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp3-30739_rabbit-son-pab-235202514492369.png)
![Immunohistochemistry-Paraffin: SON Antibody - BSA Free [NBP3-30739] - Immunochemical staining of human SON in human small intestine with NBP3-30739 at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp3-30739_rabbit-son-pab-235202514371322.png)
![Immunohistochemistry: RBM14 Antibody [NBP3-14796] - Immunochemical staining of human RBM14 in human brain with rabbit polyclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/RBM14-Antibody-Immunohistochemistry-NBP3-14796-img0003.jpg "Immunohistochemistry: RBM14 Antibody [NBP3-14796] - Immunochemical staining of human RBM14 in human brain with rabbit polyclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry: RBM14 Antibody [NBP3-14796] - Immunochemical staining of human RBM14 in human placenta with rabbit polyclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/RBM14-Antibody-Immunohistochemistry-NBP3-14796-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: RBM14 Antibody [NBP3-14796] - Immunofluorescence staining of RBM14 in A431 cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP3-14796 antibody (dilution ratio 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 Nucleus.](http://images.novusbio.com/fullsize/nbp3-14796_rabbit-rbm14-pab-235202521451788.png)
![Western Blot: NIPBL Antibody [NBP1-77974] - Detection of a band ~300 kDa corresponding to IDN3 (arrowhead) in human kidney (lane 1) and human heart (lane 2) whole cell tissue extracts. Approximately 20ug of each lysate was separated by SDS-PAGE and transferred onto nitrocellulose. After blocking the membrane was probed with the primary antibody diluted to 1:500. Use HRP conjugated Rb-a-Goat IgG [H&L] MXHu for detection.](http://images.novusbio.com/fullsize/NIPBL-Antibody-Western-Blot-NBP1-77974-img0002.jpg "Western Blot: NIPBL Antibody [NBP1-77974] - Detection of a band ~300 kDa corresponding to IDN3 (arrowhead) in human kidney (lane 1) and human heart (lane 2) whole cell tissue extracts. Approximately 20ug of each lysate was separated by SDS-PAGE and transferred onto nitrocellulose. After blocking the membrane was probed with the primary antibody diluted to 1:500. Use HRP conjugated Rb-a-Goat IgG [H&L] MXHu for detection.")
![Western Blot: NIPBL Antibody [NBP1-77974] - Shows detection of bands at ~315 kDa and ~125 kDa corresponding to isoforms of IDN3 (arrow-heads) in mouse heart whole cell tissue extract. Approximately 35 ug of lysate was separated on a 4-8% gel by SDS-PAGE and transferred onto nitrocellulose. After blocking the membrane was probed with the primary antibody diluted to 1:1,500. Reaction occurred overnight at 4h followed by washes and reaction with a 1:20,000 dilution of IRDye (TM) 800 conjugated Rb-a-Goat IgG [H&L] MXHu for 45 min at room temperature.](http://images.novusbio.com/fullsize/NIPBL-Antibody-Western-Blot-NBP1-77974-img0001.jpg)
![Western Blot: PCAF Antibody [NBP1-31192] - A. 30 ug 293T whole cell lysate/extract B. 30 ug A431 whole cell lysate/extract C. 30 ug A375 whole cell lysate/extract 7.5 % SDS-PAGE PCAF antibody [C3], C-term dilution: 1:1000](http://images.novusbio.com/fullsize/PCAF-Antibody-Western-Blot-NBP1-31192-img0005.jpg "Western Blot: PCAF Antibody [NBP1-31192] - A. 30 ug 293T whole cell lysate/extract B. 30 ug A431 whole cell lysate/extract C. 30 ug A375 whole cell lysate/extract 7.5 % SDS-PAGE PCAF antibody [C3], C-term dilution: 1:1000")
![Western Blot: PCAF Antibody [NBP1-31192] - Sample (50 ug of whole cell lysate) A: Mouse brain 7. 5% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/PCAF-Antibody-Western-Blot-NBP1-31192-img0003.jpg)
![Western Blot: PCAF Antibody [NBP1-31192] - HeLa whole cell and nuclear extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PCAF antibody [C3], C-term diluted at 1:1000.](http://images.novusbio.com/fullsize/PCAF-Antibody-Western-Blot-NBP1-31192-img0004.jpg)
![Immunohistochemistry: ILF3 Antibody (7H8) [NBP3-26200] - Image of ILF3 Antibody (7H8) diluted at 1:100 and staining in paraffin-embedded human ovarian 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 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/nbp3-26200_rabbit-ilf3-mab-7h8-26220241522420.jpg "Immunohistochemistry: ILF3 Antibody (7H8) [NBP3-26200] - Image of ILF3 Antibody (7H8) diluted at 1:100 and staining in paraffin-embedded human ovarian 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 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: ILF3 Antibody (7H8) [NBP3-26200] - Image of ILF3 Antibody (7H8) diluted at 1:100 and staining in paraffin-embedded human ovarian 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 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/nbp3-26200_rabbit-ilf3-mab-7h8-2722024847197.jpg)
![Immunocytochemistry/Immunofluorescence: ILF3 Antibody (7H8) [NBP3-26200] - Staining of Hela Cells with ILF3 Antibody (7H8) 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/nbp3-26200_rabbit-ilf3-mab-7h8-282202412493614.jpg)