| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-04693-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-35666-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-93503-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-61655-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-06557-50ul | |||
![Western Blot: CSK Antibody [NB100-808] - Staining of Jurkat lysate (35 ug protein in RIPA buffer). Antibody at 0.1 ug/mL. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/CSK-Antibody-Western-Blot-NB100-808-img0001.jpg "Western Blot: CSK Antibody [NB100-808] - Staining of Jurkat lysate (35 ug protein in RIPA buffer). Antibody at 0.1 ug/mL. Detected by chemiluminescence.")
![Western Blot: Jagged 2 Antibody [NBP1-58284] - Jurkat cell lysate, concentration 0.2-1 ug/ml.](http://images.novusbio.com/fullsize/Jagged-2-Antibody-Western-Blot-NBP1-58284-img0002.jpg "Western Blot: Jagged 2 Antibody [NBP1-58284] - Jurkat cell lysate, concentration 0.2-1 ug/ml.")
![Immunohistochemistry: Jagged 2 Antibody [NBP1-58284] - Human Bronchial Epithelial Tissue Observed Staining: Membrane of bronchial epithelial tissue Primary Antibody Concentration: 1 : 100 Secondary Antibody: Donkey anti-Rabbit-Cy3 Secondary Antibody Concentration: 1 : 200 Magnification: 20X Exposure Time: 0.5](http://images.novusbio.com/fullsize/Jagged-2-Antibody-Immunohistochemistry-NBP1-58284-img0003.jpg)
![Western Blot: IL-5 Antibody [NBP1-69163] - Mouse Spleen lysate, concentration 0.2-1 ug/ml.](http://images.novusbio.com/fullsize/IL-5-Antibody-Western-Blot-NBP1-69163-img0003.jpg "Western Blot: IL-5 Antibody [NBP1-69163] - Mouse Spleen lysate, concentration 0.2-1 ug/ml.")
![Western Blot: MAPRE1 Antibody [NBP3-04693] - Analysis of extracts of various cell lines, using MAPRE1 antibody 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](http://images.novusbio.com/fullsize/MAPRE1-Antibody-Western-Blot-NBP3-04693-img0002.jpg "Western Blot: MAPRE1 Antibody [NBP3-04693] - Analysis of extracts of various cell lines, using MAPRE1 antibody 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")
![Immunocytochemistry/ Immunofluorescence: MAPRE1 Antibody - Azide and BSA Free [MAPRE1] - Immunofluorescence analysis of HeLa cells using MAPRE1 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/nbp3-04693_rabbit-polyclonal-mapre1-antibody-5220251636379.jpg)
![Western Blot: NUBP1 Antibody [NBP3-35666] - Western blot analysis of lysates from HepG2 cells, using NUBP1 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: 1s.](http://images.novusbio.com/fullsize/nbp3-35666_rabbit-nubp1-pab-91220241519573.jpg "Western Blot: NUBP1 Antibody [NBP3-35666] - Western blot analysis of lysates from HepG2 cells, using NUBP1 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: 1s.")
![Immunohistochemistry: NUBP1 Antibody [NBP3-35666] - Immunohistochemistry analysis of paraffin-embedded Mouse kidney using NUBP1 Rabbit pAb at dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-35666_rabbit-nubp1-pab-912202414213785.jpg)
![Western Blot: NCK2 Antibody [NBP2-93503] - Analysis of extracts of various cell lines, using NCK2 .Exposure time: 90s.](http://images.novusbio.com/fullsize/NCK2-Antibody-Western-Blot-NBP2-93503-img0002.jpg "Western Blot: NCK2 Antibody [NBP2-93503] - Analysis of extracts of various cell lines, using NCK2 .Exposure time: 90s.")
![Immunohistochemistry-Paraffin: NCK2 Antibody [NBP2-93503] - Paraffin-embedded human prostate using NCK2 .](http://images.novusbio.com/fullsize/NCK2-Antibody-Immunohistochemistry-Paraffin-NBP2-93503-img0001.jpg)
![Flow Cytometry: CD81 Antibody (2F7) [NBP1-28136] - Chinese hamster ovary cell line CHO-K1 and BALB/cAnN mouse B lymphocyte cell line A20 were stained with Hamster Anti-Mouse CD81-APC.](http://images.novusbio.com/fullsize/CD81-Antibody-2F7-Flow-Cytometry-NBP1-28136-img0004.jpg "Flow Cytometry: CD81 Antibody (2F7) [NBP1-28136] - Chinese hamster ovary cell line CHO-K1 and BALB/cAnN mouse B lymphocyte cell line A20 were stained with Hamster Anti-Mouse CD81-APC.")
![Flow Cytometry: CD81 Antibody (2F7) [NBP1-28136] - 0.1 ug/1^6 The A20 cell line, a murine B cell lymphoma, was stained with hamster anti-mouse CD81-R: PE or hamster IgG-R: PE isotype control, following which the cells were analyzed for the expression of CD81 on a flow cytometer.](http://images.novusbio.com/fullsize/CD81-Antibody-2F7-Flow-Cytometry-NBP1-28136-img0001.jpg)
![Flow Cytometry: CD81 Antibody (2F7) [NBP1-28136] - Analysis using the FITC conjugate of NBP1-28136. Staining of CHO-K1 cell line (Gray) and BALB/CAnN B lymphocyte cell line A20 (Purple).](http://images.novusbio.com/fullsize/CD81-Antibody-2F7-Flow-Cytometry-NBP1-28136-img0003.jpg)
![Western Blot: Apc11 Antibody (6F1H6) [NBP2-61655] - Analysis using ANAPC11 mAb against HEK293 (1) and ANAPC11 (AA: 1-196)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/Apc11-Antibody-6F1H6-Western-Blot-NBP2-61655-img0005.jpg "Western Blot: Apc11 Antibody (6F1H6) [NBP2-61655] - Analysis using ANAPC11 mAb against HEK293 (1) and ANAPC11 (AA: 1-196)-hIgGFc transfected HEK293 (2) cell lysate.")
![Flow Cytometry: Apc11 Antibody (6F1H6) [NBP2-61655] - Analysis of Hela cells using ANAPC11 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/Apc11-Antibody-6F1H6-Flow-Cytometry-NBP2-61655-img0002.jpg)
![Western Blot: Apc11 Antibody (6F1H6) [NBP2-61655] - Analysis using ANAPC11 mAb against human ANAPC11 (AA: 1-196) recombinant protein. (Expected MW is 46.6 kDa)](http://images.novusbio.com/fullsize/Apc11-Antibody-6F1H6-Western-Blot-NBP2-61655-img0003.jpg)
![ELISA: Apc11 Antibody (6F1H6) [NBP2-61655] - 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/Apc11-Antibody-6F1H6-ELISA-NBP2-61655-img0001.jpg)
![Western Blot: p18INK4c/CDKN2C Antibody (JE36-09) [NBP3-32690] - Western blot analysis of p18INK4c/CDKN2C on different lysates with Rabbit anti-p18INK4c/CDKN2C antibody (NBP3-32690) at 1/1,000 dilution. Lane 1: HeLa cell lysate (20 ug/Lane) Lane 2: 293T cell lysate (20 ug/Lane) Lane 3: MCF7 cell lysate (20 ug/Lane) Lane 4: A549 cell lysate (20 ug/Lane) Lane 5: Mouse skeletal muscle tissue lysate (40 ug/Lane) Lane 6: Rat skeletal muscle tissue lysate (40 ug/Lane) Predicted band size: 18 kDa Observed band size: 18 kDa Exposure time: 3 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 (NBP3-32690) 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/nbp3-32690_rabbit-p18ink4c-cdkn2c-mab-je36-09-27820241631632.jpg "Western Blot: p18INK4c/CDKN2C Antibody (JE36-09) [NBP3-32690] - Western blot analysis of p18INK4c/CDKN2C on different lysates with Rabbit anti-p18INK4c/CDKN2C antibody (NBP3-32690) at 1/1,000 dilution. Lane 1: HeLa cell lysate (20 ug/Lane) Lane 2: 293T cell lysate (20 ug/Lane) Lane 3: MCF7 cell lysate (20 ug/Lane) Lane 4: A549 cell lysate (20 ug/Lane) Lane 5: Mouse skeletal muscle tissue lysate (40 ug/Lane) Lane 6: Rat skeletal muscle tissue lysate (40 ug/Lane) Predicted band size: 18 kDa Observed band size: 18 kDa Exposure time: 3 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 (NBP3-32690) 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.")
![Immunohistochemistry: p18INK4c/CDKN2C Antibody (JE36-09) [NBP3-32690] - Immunohistochemical analysis of paraffin-embedded human skeletal muscle tissue with Rabbit anti-p18INK4c/CDKN2C antibody (NBP3-32690) at 1/500 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 (NBP3-32690) at 1/500 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/nbp3-32690_rabbit-p18ink4c-cdkn2c-mab-je36-09-298202414115420.jpg)
![Western Blot: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Western blot analysis of VE-Cadherin on different lysates with Rabbit anti-VE-Cadherin antibody (NBP3-33088) at 1/2,000 dilution. Lane 1: EA.hy926-si NT cell lysate Lane 2: EA.hy926-si VE Cadherin cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 88 kDa Observed band size: 140 kDa Exposure time: 1 minute 2 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 (NBP3-33088) 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/nbp3-33088_rabbit-ve-cadherin-mab-psh03-15-288202414191513.jpg "Western Blot: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Western blot analysis of VE-Cadherin on different lysates with Rabbit anti-VE-Cadherin antibody (NBP3-33088) at 1/2,000 dilution. Lane 1: EA.hy926-si NT cell lysate Lane 2: EA.hy926-si VE Cadherin cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 88 kDa Observed band size: 140 kDa Exposure time: 1 minute 2 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 (NBP3-33088) 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.")
![Immunocytochemistry/ Immunofluorescence: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Immunocytochemistry analysis of HeLa cells labeling VE-Cadherin with Rabbit anti-VE-Cadherin antibody (NBP3-33088) 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 Rabbit anti-VE-Cadherin antibody (NBP3-33088) at 1/100 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/nbp3-33088_rabbit-ve-cadherin-mab-psh03-15-29202410234272.jpg)
![Flow Cytometry: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Flow cytometric analysis of EA.hy926 cells labeling VE-Cadherin. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (NBP3-33088, 1μg/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/nbp3-33088_rabbit-ve-cadherin-mab-psh03-15-2920241645321.jpg)
![Immunohistochemistry-Paraffin: Cyclin T1 Antibody [NBP3-06557] - Staining of human CCNT1 in human lymph node with rabbit polyclonal antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/Cyclin-T1-Antibody-Immunohistochemistry-Paraffin-NBP3-06557-img0002.jpg "Immunohistochemistry-Paraffin: Cyclin T1 Antibody [NBP3-06557] - Staining of human CCNT1 in human lymph node with rabbit polyclonal antibody at 1:500 dilution.")
![Immunohistochemistry-Paraffin: Cyclin T1 Antibody [NBP3-06557] - Staining of human CCNT1 in human adrenal gland with rabbit polyclonal antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/Cyclin-T1-Antibody-Immunohistochemistry-Paraffin-NBP3-06557-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: Cyclin T1 Antibody [NBP3-06557] - Staining of CCNT1 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 NBP3-06557 antibody (dilution ratio 1:200) 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/nbp3-06557_rabbit-polyclonal-cyclin-t1-antibody-23520252135186.png)