| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-43666-25ul | |||
| Azide and BSA Free | NBP3-44172 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-61714-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-21805-0.1ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-84588-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-43888 | |||
| BSA Free | NBP2-34476-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-49172-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-35089-20ul | |||
![Western Blot: RAP1A Antibody (1D2-1C64) [NBP2-22526] - Analysis of 25 ug of various whole cell lysates per well.](http://images.novusbio.com/fullsize/RAP1A-Antibody-1D2-1C64-Western-Blot-NBP2-22526-img0001.jpg "Western Blot: RAP1A Antibody (1D2-1C64) [NBP2-22526] - Analysis of 25 ug of various whole cell lysates per well.")
![Immunocytochemistry/Immunofluorescence: RAP1A Antibody (1D2-1C64) [NBP2-22526] - Analysis of Rap1 (green) showing staining in the in the cytoplasm of C2C12 cells (right) compared to a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RAP1A-Antibody-1D2-1C64-Immunocytochemistry-Immunofluorescence-NBP2-22526-img0006.jpg)
![Immunohistochemistry: RAP1A Antibody (1D2-1C64) [NBP2-22526] - Analysis of Rap1 showing staining in the membrane of human kidney tissue (right) compared with a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RAP1A-Antibody-1D2-1C64-Immunohistochemistry-NBP2-22526-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: RAP1A Antibody (1D2-1C64) [NBP2-22526] - Analysis of Rap1 (green) in HeLa cells. Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% BSA/TBST for 15 minutes at room temperature. Cells were probed with a Rap1 monoclonal antibody at a dilution of 1:100 for at least 1 hour at room temperature, washed with PBS, and incubated with DyLight 488-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1:400 for 30 minutes at room temperature. Nuclei (blue) were stained with Hoechst 33342 dye.](http://images.novusbio.com/fullsize/RAP1A-Antibody-1D2-1C64-Immunocytochemistry-Immunofluorescence-NBP2-22526-img0003.jpg)
![Immunoprecipitation: RAP1A Antibody (1D2-1C64) [NBP2-22526] - Analysis of Rap1 was performed on NIH3T3 cells. Antigen-antibody complexes were formed by incubating 750ug of NIH3T3 cell lysate with 2ug of a Rap1 monoclonal antibody overnight on a rocking platform at 4C. The immune complexes were captured on 50ul Protein A/G Plus Agarose, washed extensively, and eluted with 5X Lane Marker Reducing Sample Buffer. Eluted sample (right lane) and 25ug of NIH3T3 control lysate (left lane) were resolved on a 4-20% Tris-HCl polyacrylamide gel, transferred to a PVDF membrane, and blocked with 5% BSA/TBS-0.1%Tween for at least 1 hour. The membrane was probed with a Rap1 monoclonal antibody at a dilution of 1:500 overnight rotating at 4C, washed in TBST, and probed with Clean-blot IP Detection Reagent at a dilution of 1:2500 for at least 1 hour. Chemiluminescent detection was performed using SuperSignal West Dura.](http://images.novusbio.com/fullsize/RAP1A-Antibody-1D2-1C64-Immunoprecipitation-NBP2-22526-img0002.jpg)
![Western Blot: BIN1 Antibody (3B6F10) [NBP2-61714] - Analysis using BIN1 mAb against HEK293 (1) and BIN1 (AA: 189-398)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/BIN1-Antibody-3B6F10-Western-Blot-NBP2-61714-img0005.jpg "Western Blot: BIN1 Antibody (3B6F10) [NBP2-61714] - Analysis using BIN1 mAb against HEK293 (1) and BIN1 (AA: 189-398)-hIgGFc transfected HEK293 (2) cell lysate.")
![Immunohistochemistry: BIN1 Antibody (3B6F10) [NBP2-61714] - Analysis of paraffin-embedded cervical cancer tissues using BIN1 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/BIN1-Antibody-3B6F10-Immunohistochemistry-NBP2-61714-img0003.jpg)
![Flow Cytometry: BIN1 Antibody (3B6F10) [NBP2-61714] - Analysis of Hela cells using BIN1 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/BIN1-Antibody-3B6F10-Flow-Cytometry-NBP2-61714-img0002.jpg)
![Western Blot: BIN1 Antibody (3B6F10) [NBP2-61714] - Analysis using BIN1 mAb against human BIN1 (AA: 189-398) recombinant protein. (Expected MW is 47.1 kDa)](http://images.novusbio.com/fullsize/BIN1-Antibody-3B6F10-Western-Blot-NBP2-61714-img0004.jpg)
![Western Blot: BIN1 Antibody (3B6F10) [NBP2-61714] - Analysis using BIN1 mouse mAb against C2C12 (1), A431 (2), HEK293 (3), and MCF-7 (4) cell lysate.](http://images.novusbio.com/fullsize/BIN1-Antibody-3B6F10-Western-Blot-NBP2-61714-img0006.jpg)
![ELISA: BIN1 Antibody (3B6F10) [NBP2-61714] - 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/BIN1-Antibody-3B6F10-ELISA-NBP2-61714-img0001.jpg)
![Western Blot: E-Cadherin [p Ser838, p Ser840] Antibody [NBP3-12922] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with E-Cadherin (phospho Ser838/840) antibody (NBP3-12922) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/E-Cadherin-[p-Ser838--p-Ser840]-Antibody-Western-Blot-NBP3-12922-img0004.jpg "Western Blot: E-Cadherin [p Ser838, p Ser840] Antibody [NBP3-12922] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with E-Cadherin (phospho Ser838/840) antibody (NBP3-12922) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: E-Cadherin [p Ser838, p Ser840] Antibody [NBP3-12922] - E-Cadherin (phospho Ser838/840) antibody detects E-Cadherin (phospho Ser838/840) protein by western blot analysis. MCF-7 whole cell extract (30 ug) with the indicated treatments were separated by 5% SDS-PAGE, and the membrane was blotted with E-Cadherin (phospho Ser838/840) antibody (NBP3-12922) at a dilution of 1:10000.](http://images.novusbio.com/fullsize/E-Cadherin-[p-Ser838--p-Ser840]-Antibody-Western-Blot-NBP3-12922-img0001.jpg)
![Western Blot: E-Cadherin [p Ser838, p Ser840] Antibody [NBP3-12922] - E-Cadherin (phospho Ser838/840) antibody detects E-Cadherin (phospho Ser838/840) protein by western blot analysis. Rat tissue extracts (50 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with E-Cadherin (phospho Ser838/840) antibody (NBP3-12922) diluted at 1:10000.](http://images.novusbio.com/fullsize/E-Cadherin-[p-Ser838--p-Ser840]-Antibody-Western-Blot-NBP3-12922-img0002.jpg)
![Immunoprecipitation: E-Cadherin [p Ser838, p Ser840] Antibody [NBP3-12922] - Immunoprecipitation of E-Cadherin (phospho Ser838/840) protein from MCF-7 whole cell extracts using 5 ug of E-Cadherin (phospho Ser838/840) antibody (NBP3-12922). Western blot analysis was performed using E-Cadherin (phospho Ser838/840) antibody (NBP3-12922). EasyBlot anti-Rabbit IgG was used as a secondary reagent.](http://images.novusbio.com/fullsize/E-Cadherin-[p-Ser838--p-Ser840]-Antibody-Immunoprecipitation-NBP3-12922-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: N-Cadherin Antibody (GC-4) [NBP2-21805] - HeLa cells were fixed and permeabilized with methanol followed by methanol:acetone. Fixed cells were stained with Monoclonal Anti-N-Cadherin, Clone: GC-4. The antibody was developed using Goat Anti-Mouse IgG, Cy3 conjugate. Cells were counterstained with DAPI (blue) to stain nuclei.](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-GC-4-Immunofluorescence-NBP2-21805-img0002.jpg "Immunocytochemistry/Immunofluorescence: N-Cadherin Antibody (GC-4) [NBP2-21805] - HeLa cells were fixed and permeabilized with methanol followed by methanol:acetone. Fixed cells were stained with Monoclonal Anti-N-Cadherin, Clone: GC-4. The antibody was developed using Goat Anti-Mouse IgG, Cy3 conjugate. Cells were counterstained with DAPI (blue) to stain nuclei.")
![Immunohistochemistry: N-Cadherin Antibody (GC-4) [NBP2-21805] - Frozen acetone fixed chicken cardiac sections stained with Monoclonal Anti-N-Cadherin antibody produced in Mouse clone GC-4: followed by Anti-Mouse IgG (Fab specific)-FITC antibody produced in Goat.](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-GC-4-Immunohistochemistry-NBP2-21805-img0001.jpg)
![Immunohistochemistry: E-Cadherin Antibody (SY0287) [NBP3-32290] - Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-E-Cadherin antibody (NBP3-32290) at 1/200 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 (NBP3-32290) at 1/200 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/nbp3-32290_rabbit-e-cadherin-mab-sy0287-29820241435227.jpg "Immunohistochemistry: E-Cadherin Antibody (SY0287) [NBP3-32290] - Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-E-Cadherin antibody (NBP3-32290) at 1/200 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 (NBP3-32290) at 1/200 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.")
![Immunohistochemistry: E-Cadherin Antibody (SY0287) [NBP3-32290] - Immunofluorescence analysis of paraffin-embedded human colon tissue labeling E-Cadherin with Rabbit anti-E-Cadherin antibody (NBP3-32290) at 1/50 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32290, green) at 1/50 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with 33258 (blue).](http://images.novusbio.com/fullsize/nbp3-32290_rabbit-e-cadherin-mab-sy0287-29820241435238.jpg)
![Immunocytochemistry/ Immunofluorescence: E-Cadherin Antibody (SY0287) [NBP3-32290] - Immunocytochemistry analysis of HT-29 (positive) and MDA-MB-231 (negative) cells labeling E-Cadherin with Rabbit anti-E-Cadherin antibody (NBP3-32290) at 1/2,000 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-E-Cadherin antibody (NBP3-32290) at 1/2,000 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/nbp3-32290_rabbit-e-cadherin-mab-sy0287-29202410484863.jpg)
![Flow Cytometry: E-Cadherin Antibody (SY0287) [NBP3-32290] - Flow cytometric analysis of HT-29 (positive, red) and MDA-MB-231 (negative, green) cells labeling E-Cadherin. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32290, red) at 1/1,000 dilution, compared with Rabbit IgG Isotype Control (HT-29 black, MDA-MB-231 light green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with an iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃.](http://images.novusbio.com/fullsize/nbp3-32290_rabbit-e-cadherin-mab-sy0287-29202416453231.jpg)
![Western Blot: E-Cadherin Antibody (SY0287) [NBP3-32290] - Western blot analysis of E-Cadherin on different lysates with Rabbit anti-E-Cadherin antibody (NBP3-32290) at 1/5,000 dilution. Lane 1: MCF7 cell lysate Lane 2: MDA-MB-231 cell lysate (negative) Lane 3: HT-29 cell lysate Lane 4: HCT 116 cell lysate Lane 5: A431 cell lysate Lane 6: Caco-2 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 97 kDa Observed band size: 80~120 kDa Exposure time: 43 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 at 1/5,000 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/nbp3-32290_rabbit-e-cadherin-mab-sy0287-3920248453539.jpg)
![Immunocytochemistry/Immunofluorescence: BIN1 Antibody [NBP2-15587] - BIN1 antibody detects BIN1 protein at cytoplasm by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: BIN1 stained by BIN1 antibody diluted at 1:500. Blue: Fluoroshield with DAPI. Scale bar= 10 um.](http://images.novusbio.com/fullsize/BIN1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-15587-img0008.jpg "Immunocytochemistry/Immunofluorescence: BIN1 Antibody [NBP2-15587] - BIN1 antibody detects BIN1 protein at cytoplasm by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: BIN1 stained by BIN1 antibody diluted at 1:500. Blue: Fluoroshield with DAPI. Scale bar= 10 um.")
![Immunohistochemistry-Paraffin: BIN1 Antibody [NBP2-15587] - BIN1 antibody detects BIN1 protein at cytoplasm in human papillary adenocarcinoma by immunohistochemical analysis. Sample: Paraffin-embedded human papillary adenocarcinoma. BIN1 antibody diluted at 1:500.](http://images.novusbio.com/fullsize/BIN1-Antibody-Immunohistochemistry-Paraffin-NBP2-15587-img0005.jpg)
![Western Blot: BIN1 Antibody [NBP2-15587] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with BIN1 antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/BIN1-Antibody-Western-Blot-NBP2-15587-img0006.jpg)
![Western Blot: BIN1 Antibody [NBP2-15587] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with BIN1 antibody diluted at 1:2000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/BIN1-Antibody-Western-Blot-NBP2-15587-img0007.jpg)
![Immunohistochemistry-Paraffin: BIN1 Antibody [NBP2-15587] - Immunohistochemical analysis of paraffin-embedded U87 xenograft, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/BIN1-Antibody-Immunohistochemistry-Paraffin-NBP2-15587-img0003.jpg)
![Immunohistochemistry-Paraffin: E-Cadherin Antibody [NBP1-84588] - Staining of human testis shows no positivity in cells in seminiferous ducts as expected.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-Immunohistochemistry-Paraffin-NBP1-84588-img0005.jpg "Immunohistochemistry-Paraffin: E-Cadherin Antibody [NBP1-84588] - Staining of human testis shows no positivity in cells in seminiferous ducts as expected.")
![Immunohistochemistry-Paraffin: E-Cadherin Antibody [NBP1-84588] - Staining of human colon shows moderate positivity in plasma membrane in glandular cells.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-Immunohistochemistry-Paraffin-NBP1-84588-img0002.jpg)
![Immunohistochemistry-Paraffin: E-Cadherin Antibody [NBP1-84588] - Staining of human fallopian tube shows moderate positivity in plasma membrane of glandular cells.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-Immunohistochemistry-Paraffin-NBP1-84588-img0003.jpg)
![Immunohistochemistry-Paraffin: E-Cadherin Antibody [NBP1-84588] - Staining of human prostate shows moderate positivity in plasma membrane in glandular cells.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-Immunohistochemistry-Paraffin-NBP1-84588-img0004.jpg)
![Western Blot: E-Cadherin Antibody (CL1172) [NBP2-34476] - Lane 1: Marker [kDa,Lane 2: Human cell line MCF-7, Lane 3: Human cell line SK-BR-3, Lane 4: Human cell line HeLa](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-CL1172-Western-Blot-NBP2-34476-img0009.jpg "Western Blot: E-Cadherin Antibody (CL1172) [NBP2-34476] - Lane 1: Marker [kDa,Lane 2: Human cell line MCF-7, Lane 3: Human cell line SK-BR-3, Lane 4: Human cell line HeLa")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: E-Cadherin Antibody (CL1172) [NBP2-34476] - Staining in human duodenum and cerebral cortex tissues. Corresponding CDH1 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-CL1172-Immunohistochemistry-Paraffin-NBP2-34476-img0014.jpg)
![Immunohistochemistry-Paraffin: E-Cadherin Antibody (CL1172) [NBP2-34476] - Staining of human prostate shows strong membranous positivity in glandular cells.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-CL1172-Immunohistochemistry-Paraffin-NBP2-34476-img0011.jpg)
![Immunohistochemistry-Paraffin: E-Cadherin Antibody (CL1172) [NBP2-34476] - Staining of human colorectal cancer shows strong membranous positivity in tumor cells.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-CL1172-Immunohistochemistry-Paraffin-NBP2-34476-img0012.jpg)
![Immunohistochemistry-Paraffin: E-Cadherin Antibody (CL1172) [NBP2-34476] - Staining of human cerebral cortex shows no positivity in neuronal cells as expected.](http://images.novusbio.com/fullsize/E-Cadherin-Antibody-CL1172-Immunohistochemistry-Paraffin-NBP2-34476-img0013.jpg)
![Western Blot: p190RhoGAP Antibody [NBP2-49172] - Analysis in human cell line WM-115.](http://images.novusbio.com/fullsize/p190RhoGAP-Antibody-Western-Blot-NBP2-49172-img0006.jpg "Western Blot: p190RhoGAP Antibody [NBP2-49172] - Analysis in human cell line WM-115.")
![Immunohistochemistry-Paraffin: p190RhoGAP Antibody [NBP2-49172] - Staining of human fallopian tube shows strong membranous positivity in glandular cells.](http://images.novusbio.com/fullsize/p190RhoGAP-Antibody-Immunohistochemistry-Paraffin-NBP2-49172-img0005.jpg)
![Immunohistochemistry-Paraffin: p190RhoGAP Antibody [NBP2-49172] - Staining of human breast shows strong cytoplasmic positivity in glandular cells.](http://images.novusbio.com/fullsize/p190RhoGAP-Antibody-Immunohistochemistry-NBP2-49172-img0001.jpg)
![Immunohistochemistry-Paraffin: p190RhoGAP Antibody [NBP2-49172] - Staining of human testis shows moderate membranous and cytoplasmic positivity in cells in seminiferous ducts.](http://images.novusbio.com/fullsize/p190RhoGAP-Antibody-Immunohistochemistry-Paraffin-NBP2-49172-img0002.jpg)
![Immunohistochemistry-Paraffin: p190RhoGAP Antibody [NBP2-49172] - Staining of human cerebral cortex shows strong cytoplasmic positivity in neuronal cells.](http://images.novusbio.com/fullsize/p190RhoGAP-Antibody-Immunohistochemistry-Paraffin-NBP2-49172-img0003.jpg)
![Immunohistochemistry-Paraffin: p190RhoGAP Antibody [NBP2-49172] - Staining of human heart muscle shows strong cytoplasmic positivity in cardiomyocytes.](http://images.novusbio.com/fullsize/p190RhoGAP-Antibody-Immunohistochemistry-Paraffin-NBP2-49172-img0004.jpg)
![Western Blot: LIS1 Antibody [NB100-1040] - Staining of Rat Ovary lysate with antibody at 0.3 ug/mL (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/LIS1-Antibody-Western-Blot-NB100-1040-img0006.jpg "Western Blot: LIS1 Antibody [NB100-1040] - Staining of Rat Ovary lysate with antibody at 0.3 ug/mL (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: LIS1 Antibody [NB100-1040] - Staining of paraffin embedded Human Cortex. Antibody at 3.75 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](http://images.novusbio.com/fullsize/LIS1-Antibody-Immunohistochemistry-Paraffin-NB100-1040-img0005.jpg)
![Immunohistochemistry-Paraffin: LIS1 Antibody [NB100-1040] - Staining of paraffin embedded Human Pancreas. Antibody at 3.75 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](http://images.novusbio.com/fullsize/LIS1-Antibody-Immunohistochemistry-Paraffin-NB100-1040-img0003.jpg)
![Immunohistochemistry-Paraffin: LIS1 Antibody [NB100-1040] - Staining of paraffin embedded Human Thyroid. Antibody at 3.75 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](http://images.novusbio.com/fullsize/LIS1-Antibody-Immunohistochemistry-Paraffin-NB100-1040-img0004.jpg)
![Immunohistochemistry: RAP1A Antibody [NBP3-35089] - Immunohistochemistry analysis of paraffin-embedded Human liver cancer using [KO Validated] RAP1A Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-35089_rabbit-rap1a-pab-10122024121014.jpg "Immunohistochemistry: RAP1A Antibody [NBP3-35089] - Immunohistochemistry analysis of paraffin-embedded Human liver cancer using [KO Validated] RAP1A Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.")
![Immunohistochemistry: RAP1A Antibody [NBP3-35089] - Immunohistochemistry analysis of paraffin-embedded Mouse spleen using [KO Validated] RAP1A Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-35089_rabbit-rap1a-pab-101220241224118.jpg)
![Western Blot: RAP1A Antibody [NBP3-35089] - Western blot analysis of lysates from wild type(WT) and RAP1A knockdown (KD) 293T cells, using [KO Validated] RAP1A 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: 90s.](http://images.novusbio.com/fullsize/nbp3-35089_rabbit-rap1a-pab-1012202411552841.jpg)
![Immunohistochemistry: RAP1A Antibody [NBP3-35089] - Immunohistochemistry analysis of paraffin-embedded Human colon carcinoma using [KO Validated] RAP1A Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-35089_rabbit-rap1a-pab-1012202411592829.jpg)
![Western Blot: RAP1A Antibody [NBP3-35089] - Western blot analysis of various lysates using [KO Validated] RAP1A 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: 90s.](http://images.novusbio.com/fullsize/nbp3-35089_rabbit-rap1a-pab-1012202411535893.jpg)