| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-91837-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-70448 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89836-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-03603-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-03316-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98294-50ul | |||
![Western Blot: CRABP2 Antibody [NB100-2590] - Whole cell lysate (5, 15 and 50 ug) from MCF7 cells. Antibody used at 0.04 ug/ml.](http://images.novusbio.com/fullsize/CRABP2-Antibody-Western-Blot-NB100-2590-img0007.jpg "Western Blot: CRABP2 Antibody [NB100-2590] - Whole cell lysate (5, 15 and 50 ug) from MCF7 cells. Antibody used at 0.04 ug/ml.")
![Immunohistochemistry-Paraffin: CRABP2 Antibody [NB100-2590] - Section of human prostate carcinoma. Antibody: Affinity purified rabbit anti-CRABP2 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/CRABP2-Antibody-Immunohistochemistry-Paraffin-NB100-2590-img0009.jpg)
![Western Blot: Dlx1 Antibody [NBP1-91837] - Analysis in human cell line HEK 293](http://images.novusbio.com/fullsize/Dlx1-Antibody-Western-Blot-NBP1-91837-img0006.jpg "Western Blot: Dlx1 Antibody [NBP1-91837] - Analysis in human cell line HEK 293")
![Immunohistochemistry-Paraffin: Dlx1 Antibody [NBP1-91837] - Staining of human cerebellum shows strong positivity in nerve fibers.](http://images.novusbio.com/fullsize/Dlx1-Antibody-Immunohistochemistry-Paraffin-NBP1-91837-img0004.jpg)
![Western Blot: Dlx1 Antibody [NBP1-91837] - Analysis in control (vector only transfected HEK293T lysate) and DLX1 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).](http://images.novusbio.com/fullsize/Dlx1-Antibody-Western-Blot-NBP1-91837-img0005.jpg)
![Western Blot: CRABP2 Antibody (10D6) [NBP2-03807] Analysis of extracts (35ug) from 9 different cell lines by usin g anti-CRABP2 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).](http://images.novusbio.com/fullsize/CRABP2-Antibody-10D6-Western-Blot-NBP2-03807-img0004.jpg "Western Blot: CRABP2 Antibody (10D6) [NBP2-03807] Analysis of extracts (35ug) from 9 different cell lines by usin g anti-CRABP2 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).")
![Immunohistochemistry-Paraffin: CRABP2 Antibody (10D6) [NBP2-03807] - Staining of paraffin-embedded Adenocarcinoma of Human ovary tissue using anti-CRABP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/CRABP2-Antibody-10D6-Immunohistochemistry-Paraffin-NBP2-03807-img0003.jpg)
![Flow Cytometry: CRABP2 Antibody (10D6) [NBP2-03807] - HEK293T cells transfected with either overexpression plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-CRABP2 antibody, and then analyzed by flow cytometry.](http://images.novusbio.com/fullsize/CRABP2-Antibody-10D6-Flow-Cytometry-NBP2-03807-img0001.jpg)
![Western Blot: CRABP2 Antibody (10D6) [NBP2-03807] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CRABP2 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-CRABP2.](http://images.novusbio.com/fullsize/CRABP2-Antibody-10D6-Western-Blot-NBP2-03807-img0002.jpg)
![Western Blot: CRABP2 Antibody (004) [NBP2-89836] - Lane A: 293T Whole Cell Lysate Lane B: MCF7 Whole Cell LysateLysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:16 kDa Observed band size:14 kDa](http://images.novusbio.com/fullsize/CRABP2-Antibody-004-Western-Blot-NBP2-89836-img0002.jpg "Western Blot: CRABP2 Antibody (004) [NBP2-89836] - Lane A: 293T Whole Cell Lysate Lane B: MCF7 Whole Cell LysateLysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:16 kDa Observed band size:14 kDa")
![<b>Biological Strategies Validation. </b>Flow Cytometry: CRABP2 Antibody (004) [NBP2-89836] - Analysis of Human CRABP2 expression on MCF-7 cells. The cells were treated , stained with purified anti-Human CRABP2, 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/CRABP2-Antibody-004-Flow-Cytometry-NBP2-89836-img0004.jpg)
![Immunoprecipitation: CRABP2 Antibody (004) [NBP2-89836] - Lane A:0.5 mg 293T Whole Cell Lysate Lane B:0.5 mg Raji Whole Cell Lysate0.5 uL anti-CRABP2 rabbit monoclonal antibody and 60 ug of Immunomagnetic beads Protein G. Primary antibody: Anti-CRABP2 rabbit monoclonal antibody,at 1:500 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: 16 kDa Observed band size: 16 kDa](http://images.novusbio.com/fullsize/CRABP2-Antibody-004-Immunoprecipitation-NBP2-89836-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: CRABP2 Antibody (004) [NBP2-89836] - Staining of Human CRABP2 in MCF7 cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89836 antibody (1:300) 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 cytoplasm.](http://images.novusbio.com/fullsize/nbp2-89836_rabbit-monoclonal-crabp2-antibody-004-235202514331567.png)
![Western Blot: Endothelin-3 Antibody (2A6-2A4) [H00001908-M01] - Analysis of EDN3 expression in transfected 293T cell line by EDN3 monoclonal antibody (M01), clone 2A6-2A4.Lane 1: EDN3 transfected lysate(25.5 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/Endothelin-3-Antibody-2A6-2A4-Western-Blot-H00001908-M01-img0006.jpg "Western Blot: Endothelin-3 Antibody (2A6-2A4) [H00001908-M01] - Analysis of EDN3 expression in transfected 293T cell line by EDN3 monoclonal antibody (M01), clone 2A6-2A4.Lane 1: EDN3 transfected lysate(25.5 KDa).Lane 2: Non-transfected lysate.")
![Western Blot: Endothelin-3 Antibody (2A6-2A4) [H00001908-M01] - EDN3 monoclonal antibody (M01), clone 2A6-2A4 Analysis of EDN3 expression in LNCaP.](http://images.novusbio.com/fullsize/Endothelin-3-Antibody-2A6-2A4-Western-Blot-H00001908-M01-img0005.jpg)
![Immunoprecipitation: Endothelin-3 Antibody (2A6-2A4) [H00001908-M01] - Analysis of EDN3 transfected lysate using anti-EDN3 monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with EDN3 MaxPab rabbit polyclonal antibody.](http://images.novusbio.com/fullsize/Endothelin-3-Antibody-2A6-2A4-Immunoprecipitation-H00001908-M01-img0003.jpg)
![ELISA: Endothelin-3 Antibody (2A6-2A4) [H00001908-M01] - Detection limit for recombinant GST tagged EDN3 is approximately 0.3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/Endothelin-3-Antibody-2A6-2A4-ELISA-H00001908-M01-img0004.jpg)
![Western Blot: Dlx1 Antibody [NBP2-16178] - Various tissue extracts (50 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with Dlx1 antibody [N1C3-2] 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/Dlx1-Antibody-Western-Blot-NBP2-16178-img0003.jpg "Western Blot: Dlx1 Antibody [NBP2-16178] - Various tissue extracts (50 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with Dlx1 antibody [N1C3-2] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: Dlx1 Antibody [NBP2-16178] - Sample (30 ug of whole cell lysate) A: U87-MG 12% SDS PAGE gel, diluted at 1:3000.](http://images.novusbio.com/fullsize/Dlx1-Antibody-Western-Blot-NBP2-16178-img0001.jpg)
![Western Blot: SELENBP1 Antibody [NBP3-03603] - Analysis of extracts of various cell lines, using SELENBP1 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/SELENBP1-Antibody-Western-Blot-NBP3-03603-img0004.jpg "Western Blot: SELENBP1 Antibody [NBP3-03603] - Analysis of extracts of various cell lines, using SELENBP1 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: SELENBP1 Antibody [NBP3-03603] - Analysis of HeLa cells using SELENBP1 antibody . Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/SELENBP1-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-03603-img0001.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: SELENBP1 Antibody [NBP3-03603] - Analysis of extracts from normal (control) and SELENBP1 knockout (KO) HeLa cells, using SELENBP1 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. BBlocking buffer: 3% nonfat dry milk in TBST.](http://images.novusbio.com/fullsize/SELENBP1-Antibody-Knockout-Validated-NBP3-03603-img0003.jpg)
![Western Blot: Frequenin Antibody [NBP3-03316] - Analysis of extracts of various cell lines, using Frequenin 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/Frequenin-Antibody-Western-Blot-NBP3-03316-img0002.jpg "Western Blot: Frequenin Antibody [NBP3-03316] - Analysis of extracts of various cell lines, using Frequenin 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: Frequenin Antibody - BSA Free [NBP3-03316] - Immunofluorescence analysis of A549 cells using Frequenin antibody (A13586). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-03316_rabbit-polyclonal-frequenin-antibody-52202519313430.jpg)
![Immunohistochemistry-Paraffin: CRABP2 Antibody [NBP2-98294] - Immunochemical staining of mouse CRABP2 in mouse liver with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/CRABP2-Antibody-Immunohistochemistry-Paraffin-NBP2-98294-img0003.jpg "Immunohistochemistry-Paraffin: CRABP2 Antibody [NBP2-98294] - Immunochemical staining of mouse CRABP2 in mouse liver with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: CRABP2 Antibody [NBP2-98294] - Immunochemical staining of mouse CRABP2 in mouse kidney with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/CRABP2-Antibody-Immunohistochemistry-Paraffin-NBP2-98294-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CRABP2 Antibody [NBP2-98294] - Immunofluorescence staining of mCRABP2 in NIH-3T3 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98294 antibody (dilution ratio 1:200) 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 Cytoplasm.](http://images.novusbio.com/fullsize/nbp2-98294_rabbit-polyclonal-crabp2-antibody-23520251129330.png)
![Western Blot: CRABP2 Antibody (S01-4C4) [NBP3-19505] - Western blot detection of CRABP2 in Hela cell lysates using NBP3-19505 (1:1000 diluted). Predicted band size: 16kDa. Observed band size: 14kDa.](http://images.novusbio.com/fullsize/CRABP2-Antibody-S01-4C4-Western-Blot-NBP3-19505-img0002.jpg "Western Blot: CRABP2 Antibody (S01-4C4) [NBP3-19505] - Western blot detection of CRABP2 in Hela cell lysates using NBP3-19505 (1:1000 diluted). Predicted band size: 16kDa. Observed band size: 14kDa.")
![Immunocytochemistry/Immunofluorescence: CRABP2 Antibody (S01-4C4) [NBP3-19505] - Immunofluorescence of CRABP2 (green) in MCF-7 using NBP3-19505 at dilution 1/20, and DAPI (blue)](http://images.novusbio.com/fullsize/nbp3-19505_rabbit-crabp2-mab-s01-4c4-11320251514545.jpg)
![Western Blot: CRABP2 Antibody (JE65-66) [NBP3-32214] - Western blot analysis of CRABP2 on MCF-7 cell lysates with Rabbit anti-CRABP2 antibody (NBP3-32214) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 16 kDa Observed band size: 14 kDa Exposure time: 2 minutes; 15% 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 (NBP3-32214) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32214_rabbit-crabp2-mab-je65-66-278202415242666.jpg "Western Blot: CRABP2 Antibody (JE65-66) [NBP3-32214] - Western blot analysis of CRABP2 on MCF-7 cell lysates with Rabbit anti-CRABP2 antibody (NBP3-32214) at 1/1,000 dilution. Lysates/proteins at 10 ug/Lane. Predicted band size: 16 kDa Observed band size: 14 kDa Exposure time: 2 minutes; 15% 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 (NBP3-32214) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CRABP2 Antibody (JE65-66) [NBP3-32214] - Immunohistochemical analysis of paraffin-embedded human esophagus tissue with Rabbit anti-CRABP2 antibody (NBP3-32214) at 1/400 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 (NBP3-32214) at 1/400 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/nbp3-32214_rabbit-crabp2-mab-je65-66-298202414161824.jpg)