| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35252-1mg | |||
| Carrier-Free | NBP2-35252-100ug | |||
| Carrier-Free | NBP2-35252-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-37417-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35076-1mg | |||
| Carrier-Free | NBP2-35076-100ug | |||
| Carrier-Free | NBP2-35076-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-13078-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-05122-0.025mg | |||
![Western Blot: MIF Antibody (4E4) [NBP1-04319] - The cell lysates of HL-60 was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human MIF antibody (1:1,000). Protein was visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.](http://images.novusbio.com/fullsize/MIF-Antibody-4E4-Western-Blot-NBP1-04319-img0002.jpg "Western Blot: MIF Antibody (4E4) [NBP1-04319] - The cell lysates of HL-60 was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human MIF antibody (1:1,000). Protein was visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.")
![Immunocytochemistry/Immunofluorescence: MIF Antibody (4E4) [NBP1-04319] - Analysis of MIF in HeLa cells. The cell was stained at (1:100). The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue).](http://images.novusbio.com/fullsize/MIF-Antibody-4E4-Immunocytochemistry-Immunofluorescence-NBP1-04319-img0004.jpg)
![Western Blot: MIF Antibody (4E4) [NBP1-04319] - The cell lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human MIF antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.Lane 1.: Jurkat cell lysateLane 2.: THP-1 cell lysateLane 3.: HeLa cell lysateLane 4.: U937 cell lysate](http://images.novusbio.com/fullsize/MIF-Antibody-4E4-Western-Blot-NBP1-04319-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: MIF Antibody (4E4) [NBP1-04319] - Analysis of MIF in Balb/3T3 cells. The cell was stained at (1:100). The secondary antibody (green) was used Alexa Fluor 488. DAPI was stained the cell nucleus (blue).](http://images.novusbio.com/fullsize/MIF-Antibody-4E4-Immunocytochemistry-Immunofluorescence-NBP1-04319-img0003.jpg)
![Western Blot: Ets-1 Antibody (8A8) [NBP2-22169] - Western blot analysis using ETS1 mouse mAb against Jurkat (1), HepG2 (2) and ETS1-hIgGFc transfected HEK293 (3) cell lysate.](http://images.novusbio.com/fullsize/Ets-1-Antibody-8A8-Western-Blot-NBP2-22169-img0004.jpg "Western Blot: Ets-1 Antibody (8A8) [NBP2-22169] - Western blot analysis using ETS1 mouse mAb against Jurkat (1), HepG2 (2) and ETS1-hIgGFc transfected HEK293 (3) cell lysate.")
![Immunocytochemistry/Immunofluorescence: Ets-1 Antibody (8A8) [NBP2-22169] - Immunofluorescence analysis of NIH/3T3 cells using anti-ETS1 mAb (green). Blue: DRAQ5 fluorescent DNA dye.](http://images.novusbio.com/fullsize/Ets-1-Antibody-8A8-Immunocytochemistry-Immunofluorescence-NBP2-22169-img0002.jpg)
![Immunohistochemistry-Paraffin: Ets-1 Antibody (8A8) [NBP2-22169] - Immunohistochemical analysis of paraffin-embedded human Colon, Adipocytes tissues using anti-ETS1 mouse mAb](http://images.novusbio.com/fullsize/Ets-1-Antibody-8A8-Immunohistochemistry-Paraffin-NBP2-22169-img0003.jpg)
![Flow Cytometry: Ets-1 Antibody (8A8) [NBP2-22169] - Flow cytometric analysis of Jurkat cells using anti-ETS1 mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/Ets-1-Antibody-8A8-Flow-Cytometry-NBP2-22169-img0001.jpg)
![SDS-Page: Rat IL-4 Protein [NBP2-35252]](http://images.novusbio.com/fullsize/Rat-IL-4-Protein-SDS-Page-NBP2-35252-img0001.jpg "SDS-Page: Rat IL-4 Protein [NBP2-35252]")
![Bioactivity: Recombinant Rat IL-4 Protein [NBP2-35252] - Gene expression of macrophages. Culturing with IL-4 increased Arg1 without affecting iNOS or IL-6. Rat macrophages were cultured with M-CSF. After maturation (7 days) in vitro, macrophages were cultured with with IL-4 + M-CSF or M-CSF alone. Changes in gene expression were assayed using RT-PCR using Image from verified customer review.](http://images.novusbio.com/fullsize/Recombinant-Rat-IL-4-Protein-Bioactivity-NBP2-35252-img0002.jpg)
![Western Blot: ID2 Antibody (4E12G5) [NBP2-37417] - Analysis using ID2 mAb against human ID2 recombinant protein. (Expected MW is 17.3 kDa).](http://images.novusbio.com/fullsize/ID2-Antibody-4E12G5-Western-Blot-NBP2-37417-img0002.jpg "Western Blot: ID2 Antibody (4E12G5) [NBP2-37417] - Analysis using ID2 mAb against human ID2 recombinant protein. (Expected MW is 17.3 kDa).")
![Immunohistochemistry-Paraffin: ID2 Antibody (4E12G5) [NBP2-37417] - Analysis of rectum cancer tissues using ID2 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/ID2-Antibody-4E12G5-Immunohistochemistry-NBP2-37417-img0005.jpg)
![Flow Cytometry: ID2 Antibody (4E12G5) [NBP2-37417] - Analysis of SK-N-SH cells using ID2 mouse mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/ID2-Antibody-4E12G5-Flow-Cytometry-NBP2-37417-img0003.jpg)
![Immunohistochemistry-Paraffin: ID2 Antibody (4E12G5) [NBP2-37417] - Analysis of breast cancer tissues using ID2 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/ID2-Antibody-4E12G5-Immunohistochemistry-NBP2-37417-img0004.jpg)
![ELISA: ID2 Antibody (4E12G5) [NBP2-37417] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/ID2-Antibody-4E12G5-ELISA-NBP2-37417-img0001.jpg)
![SDS-Page: Human TNF-alpha Protein [NBP2-35076]](http://images.novusbio.com/fullsize/Human-TNF-alpha-Protein-SDS-Page-NBP2-35076-img0001.jpg "SDS-Page: Human TNF-alpha Protein [NBP2-35076]")
![Western Blot: Fas/TNFRSF6/CD95 Antibody (4F8D6) - BSA Free [NBP2-13078] - Figure 3: Western blot analysis using Fas/TNFRSF6/CD95 mouse monoclonal antibody against Hela (1), Jurkat (2) cell lysate.](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-4F8D6-Western-Blot-NBP2-13078-img0003.jpg "Western Blot: Fas/TNFRSF6/CD95 Antibody (4F8D6) - BSA Free [NBP2-13078] - Figure 3: Western blot analysis using Fas/TNFRSF6/CD95 mouse monoclonal antibody against Hela (1), Jurkat (2) cell lysate.")
![Flow Cytometry: Fas/TNFRSF6/CD95 Antibody (4F8D6) - BSA Free [NBP2-13078] - Figure 4: Flow cytometric analysis of Hela cells using Fas/TNFRSF6/CD95 mouse monoclonal antibody (green) and negative control (red).](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-4F8D6-Flow-Cytometry-NBP2-13078-img0004.jpg)
![Western Blot: Fas/TNFRSF6/CD95 Antibody (4F8D6) - BSA Free [NBP2-13078] - Figure 2: Western blot analysis using Fas/TNFRSF6/CD95 monoclonal antibody against human Fas/TNFRSF6/CD95 (AA: 87-278) recombinant protein. (Expected MW is 47.2 kDa)](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-4F8D6-Western-Blot-NBP2-13078-img0002.jpg)
![ELISA: Fas Receptor/TNFRSF6/CD95 Antibody (4F8D6) [NBP2-13078] - Fas/TNFRSF6/CD95 Antibody (4F8D6) [NBP2-13078] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-4F8D6-ELISA-NBP2-13078-img0001.jpg)
![Western Blot: CD3 zeta Antibody (4B10) [NBP1-42561] - Analysis using CD247 mAb against CD247(AA: 52-164)-hIgGFc transfected HEK293 cell lysate.](http://images.novusbio.com/fullsize/CD3-zeta-Antibody-4B10-Western-Blot-NBP1-42561-img0011.jpg "Western Blot: CD3 zeta Antibody (4B10) [NBP1-42561] - Analysis using CD247 mAb against CD247(AA: 52-164)-hIgGFc transfected HEK293 cell lysate.")
![Immunocytochemistry/Immunofluorescence: CD3 zeta Antibody (4B10) [NBP1-42561] - Analysis of K562 cells using anti-CD247 mAb (green). Blue: DRAQ5 fluorescent DNA dye.](http://images.novusbio.com/fullsize/CD3-zeta-Antibody-4B10-Immunocytochemistry-Immunofluorescence-NBP1-42561-img0009.jpg)
![Immunohistochemistry-Paraffin: CD3 zeta Antibody (4B10) [NBP1-42561] - Analysis of human Thymus tissues using anti-CD247 mouse mAb](http://images.novusbio.com/fullsize/CD3-zeta-Antibody-4B10-Immunohistochemistry-Paraffin-NBP1-42561-img0010.jpg)
![Flow Cytometry: CD3 zeta Antibody (4B10) [NBP1-42561] - Analysis of Jurkat cells using anti-CD247 mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/CD3-zeta-Antibody-4B10-Flow-Cytometry-NBP1-42561-img0012.jpg)
![Immunohistochemistry: Complement C3a Antibody (K13/16-5.7) - BSA Free [NBP1-05122] - Staining in human kidney. Strong staining of plasma of nephritis kidney was seen. Dilution: 1:75.](http://images.novusbio.com/fullsize/Complement-C3a-Antibody-K13-16-5-7-BSA-Free-Immunocytochemistry-Immunofluorescence-NBP1-05122-img0011.jpg "Immunohistochemistry: Complement C3a Antibody (K13/16-5.7) - BSA Free [NBP1-05122] - Staining in human kidney. Strong staining of plasma of nephritis kidney was seen. Dilution: 1:75.")
![Western Blot: Complement C3a Antibody (K13/16-5.7) - BSA Free [NBP1-05122] - Lane 1: purified C3, lane 2: purifed C3 reduced/DTT, lane 3: purified C3a , lane 4: EDTA-plasma. Lane 5: zymosan-activated serum](http://images.novusbio.com/fullsize/Complement-C3a-Antibody-K13-16-5-7-BSA-Free-Western-Blot-NBP1-05122-img0004.jpg)
![Immunohistochemistry-Paraffin: Complement C3a Antibody (K13/16-5.7) - BSA Free [NBP1-05122] - Staining of human kidney. Strong staining of veins of nephritis kidney was seen. Dilution: 1:150.](http://images.novusbio.com/fullsize/Complement-C3a-Antibody-K13-16-5-7-BSA-Free-Immunohistochemistry-Paraffin-NBP1-05122-img0007.jpg)
![Sandwich ELISA Capture: Complement C3a Antibody (K13/16-5.7) - BSA Free [NBP1-05122] - The calibration curve of a sandwich assay for Complement C3a using NBP1-05122 as the capture antibody and NBP2-23496 as the biotinylated detection antibody.](http://images.novusbio.com/fullsize/Complement-C3a-Antibody-K13-16-5-7-BSA-Free-Sandwich-ELISA-Capture-NBP1-05122-img0005.jpg)
![Immunohistochemistry-Paraffin: CXCR3 Antibody [NBP2-77442] - Staining (8ug/ml) of paraffin embedded Human Spleen. Heat induced antigen retrieval with citrate buffer pH 6, HRP-Staining.](http://images.novusbio.com/fullsize/CXCR3-Antibody-Immunohistochemistry-Paraffin-NBP2-77442-img0004.jpg "Immunohistochemistry-Paraffin: CXCR3 Antibody [NBP2-77442] - Staining (8ug/ml) of paraffin embedded Human Spleen. Heat induced antigen retrieval with citrate buffer pH 6, HRP-Staining.")
![Flow Cytometry: CXCR3 Antibody [NBP2-77442] - Analysis of paraformaldehyde fixed HepG2 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (1 ug/mL). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/CXCR3-Antibody-Flow-Cytometry-NBP2-77442-img0003.jpg)
![Immunohistochemistry-Paraffin: CXCR3 Antibody [NBP2-77442] - Negative Control showing staining of paraffin embedded Human Spleen, with no primary antibody.](http://images.novusbio.com/fullsize/CXCR3-Antibody-Immunohistochemistry-Paraffin-NBP2-77442-img0005.jpg)
![Immunofluorescence: CXCR3 Antibody [NBP2-77442] - Analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing membrane staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/CXCR3-Antibody-Immunofluorescence-NBP2-77442-img0001.jpg)
![Immunofluorescence: CXCR3 Antibody [NBP2-77442] - Analysis of paraformaldehyde fixed HepG2 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing membrane staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/CXCR3-Antibody-Immunofluorescence-NBP2-77442-img0002.jpg)
![Western Blot: IKK beta Antibody (SN63-02) [NBP2-67659] - Western blot analysis of IKK beta on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-](http://images.novusbio.com/fullsize/IKK-beta-Antibody-SN63-02-Western-Blot-NBP2-67659-img0005.jpg "Western Blot: IKK beta Antibody (SN63-02) [NBP2-67659] - Western blot analysis of IKK beta on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-")
![Immunocytochemistry/Immunofluorescence: IKK beta Antibody (SN63-02) [NBP2-67659] - Staining IKK alpha+IKK beta in B-6F1 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/IKK-beta-Antibody-SN63-02-Immunocytochemistry-Immunofluorescence-NBP2-67659-img0004.jpg)
![Western Blot: IKK beta Antibody (SN63-02) [NBP2-67659] - Analysis of IKK alpha+IKK beta on different lysates using anti-IKK alpha+IKK beta antibody at 1/1,000 dilution. Positive control: Lane 1: Hela Lane 2: Daudi Lane 3: A431](http://images.novusbio.com/fullsize/IKK-beta-Antibody-SN63-02-Western-Blot-NBP2-67659-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: IKK beta Antibody (SN63-02) [NBP2-67659] - Staining IKK alpha+IKK beta in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/IKK-beta-Antibody-SN63-02-Immunocytochemistry-Immunofluorescence-NBP2-67659-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: IKK beta Antibody (SN63-02) [NBP2-67659] - Staining IKK alpha+IKK beta in C2C12 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/IKK-beta-Antibody-SN63-02-Immunocytochemistry-Immunofluorescence-NBP2-67659-img0002.jpg)
![Western Blot: GATA-3 Antibody (A3G3-R) [NBP3-32375] - Western blot analysis of GATA-3 on different lysates with Mouse anti-GATA-3 antibody (NBP3-32375) at 1/1,000 dilution. Lane 1: SH-SY5Y cell lysate Lane 2: MCF7 cell lysate Lane 3: Jurkat cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 48 kDa Observed band size: 48/37/25 kDa Exposure time: 1 minute; 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 (NBP3-32375) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32375_mouse-gata-3-mab-a3g3-r-27820241631676.jpg "Western Blot: GATA-3 Antibody (A3G3-R) [NBP3-32375] - Western blot analysis of GATA-3 on different lysates with Mouse anti-GATA-3 antibody (NBP3-32375) at 1/1,000 dilution. Lane 1: SH-SY5Y cell lysate Lane 2: MCF7 cell lysate Lane 3: Jurkat cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 48 kDa Observed band size: 48/37/25 kDa Exposure time: 1 minute; 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 (NBP3-32375) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: GATA-3 Antibody (A3G3-R) [NBP3-32375] - Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue with Mouse anti-GATA-3 antibody (NBP3-32375) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (NBP3-32375) 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/nbp3-32375_mouse-gata-3-mab-a3g3-r-298202414161838.jpg)
![Immunocytochemistry/ Immunofluorescence: GATA-3 Antibody (A3G3-R) [NBP3-32375] - Immunocytochemistry analysis of SH-SY5Y cells labeling GATA-3 with Mouse anti-GATA-3 antibody (NBP3-32375) 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 Mouse anti-GATA-3 antibody (NBP3-32375) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse 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-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32375_mouse-gata-3-mab-a3g3-r-29202410234242.jpg)
![Flow Cytometry: GATA-3 Antibody (A3G3-R) [NBP3-32375] - Flow cytometric analysis of SH-SY5Y cells labeling GATA-3. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32375, 1μg/mL) (red) compared with Mouse IgG1 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-Mouse 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/nbp3-32375_mouse-gata-3-mab-a3g3-r-29202416372173.jpg)
![Immunocytochemistry/Immunofluorescence: CXCL10/IP-10/CRG-2 Antibody (JA10-82) [NBP2-67004] - Staining IP10 in N2A cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CXCL10-IP-10-CRG-2-Antibody-JA10-82-Immunocytochemistry-Immunofluorescence-NBP2-67004-img0004.jpg "Immunocytochemistry/Immunofluorescence: CXCL10/IP-10/CRG-2 Antibody (JA10-82) [NBP2-67004] - Staining IP10 in N2A cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.")
![Immunohistochemistry-Paraffin: CXCL10/IP-10/CRG-2 Antibody (JA10-82) [NBP2-67004] - Human tonsil tissue using anti-IP10 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/400) for 30 minutes 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/CXCL10-IP-10-CRG-2-Antibody-JA10-82-Immunohistochemistry-Paraffin-NBP2-67004-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: CXCL10/IP-10/CRG-2 Antibody (JA10-82) [NBP2-67004] - Staining IP10 in HepG2 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CXCL10-IP-10-CRG-2-Antibody-JA10-82-Immunocytochemistry-Immunofluorescence-NBP2-67004-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: CXCL10/IP-10/CRG-2 Antibody (JA10-82) [NBP2-67004] - Staining IP10 in SH-SY5Y cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CXCL10-IP-10-CRG-2-Antibody-JA10-82-Immunocytochemistry-Immunofluorescence-NBP2-67004-img0003.jpg)
![Immunohistochemistry-Paraffin: CXCL10/IP-10/CRG-2 Antibody (JA10-82) [NBP2-67004] - Analysis of paraffin-embedded human skin tissue using anti-IP10 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CXCL10-IP-10-CRG-2-Antibody-JA10-82-Immunohistochemistry-Paraffin-NBP2-67004-img0002.jpg)