| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90577-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-98304-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89232-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99524-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99098-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-99099-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97729-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90080-50ul | |||
![Flow Cytometry: CD48/SLAMF2 Antibody (341) [NBP2-90577] - Flow cytometric analysis of Mouse CD48/SLAMF2 expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse CD48/SLAMF2, 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/CD48-SLAMF2-Antibody-341-Flow-Cytometry-NBP2-90577-img0001.jpg "Flow Cytometry: CD48/SLAMF2 Antibody (341) [NBP2-90577] - Flow cytometric analysis of Mouse CD48/SLAMF2 expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse CD48/SLAMF2, 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.")
![Immunocytochemistry/Immunofluorescence: CD48/SLAMF2 Antibody (341) [NBP2-90577] - Immunofluorescence staining of Mouse CD48/SLAMF2 in Mouse Spleen cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90577 antibody (1:60) at 37C 1 hour. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG Secondary antibody (green). Positive staining was localized to cell membrane.](http://images.novusbio.com/fullsize/nbp2-90577_rabbit-monoclonal-cd48-slamf2-antibody-341-235202514331563.png)
![Western Blot: RIPK3/RIP3 Antibody (PSH04-78) [NBP3-32905] - Western blot analysis of RIPK3/RIP3 on different lysates with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32905) at 1/2,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HT-29 cell lysate Lane 3: SK-Br-3 cell lysate Lane 4: HeLa cell lysate (negative) Lysates/proteins at 30 ug/Lane. Predicted band size: 57 kDa Observed band size: 55 kDa Exposure time: 1 minute; ECL; 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 (NBP3-32905) 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/nbp3-32905_rabbit-ripk3-rip3-mab-psh04-78-288202412461621.jpg "Western Blot: RIPK3/RIP3 Antibody (PSH04-78) [NBP3-32905] - Western blot analysis of RIPK3/RIP3 on different lysates with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32905) at 1/2,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HT-29 cell lysate Lane 3: SK-Br-3 cell lysate Lane 4: HeLa cell lysate (negative) Lysates/proteins at 30 ug/Lane. Predicted band size: 57 kDa Observed band size: 55 kDa Exposure time: 1 minute; ECL; 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 (NBP3-32905) 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.")
![Immunohistochemistry: RIPK3/RIP3 Antibody (PSH04-78) [NBP3-32905] - Immunohistochemical analysis of paraffin-embedded HT-29 (positive) and HeLa (negative) cells with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32905) at 1/5,000 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 (NBP3-32905) at 1/5,000 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/nbp3-32905_rabbit-ripk3-rip3-mab-psh04-78-298202414333611.jpg)
![Immunohistochemistry-Paraffin: Cathepsin E Antibody [NBP2-98304] - Immunochemical staining of mouse Cathepsin E in mouse stomach with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/Cathepsin-E-Antibody-Immunohistochemistry-Paraffin-NBP2-98304-img0002.jpg "Immunohistochemistry-Paraffin: Cathepsin E Antibody [NBP2-98304] - Immunochemical staining of mouse Cathepsin E in mouse stomach with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: Cathepsin E Antibody [NBP2-98304] - Immunochemical staining of mouse Cathepsin E in mouse liver with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/Cathepsin-E-Antibody-Immunohistochemistry-Paraffin-NBP2-98304-img0001.jpg)
![Immunohistochemistry-Paraffin: Cathepsin E Antibody - BSA Free [NBP2-98304] - Immunochemical staining of Cathepsin E in mouse stomach with NBP2-98304 at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp2-98304_rabbit-polyclonal-cathepsin-e-antibody-23520251628181.png)
![Western Blot: ZEB1 Antibody (JE57-64) [NBP3-33111] - Western blot analysis of ZEB1 on different lysates with Rabbit anti-ZEB1 antibody (NBP3-33111) at 1/500 dilution. Lane 1: Hela cell lysate Lane 2: HUVEC cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 124 kDa Observed band size: 200 kDa Exposure time: 3 minutes; 6% 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 (NBP3-33111) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-33111_rabbit-zeb1-mab-je57-64-288202414191510.jpg "Western Blot: ZEB1 Antibody (JE57-64) [NBP3-33111] - Western blot analysis of ZEB1 on different lysates with Rabbit anti-ZEB1 antibody (NBP3-33111) at 1/500 dilution. Lane 1: Hela cell lysate Lane 2: HUVEC cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 124 kDa Observed band size: 200 kDa Exposure time: 3 minutes; 6% 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 (NBP3-33111) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: ZEB1 Antibody (JE57-64) [NBP3-33111] - Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-ZEB1 antibody (NBP3-33111) 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 (NBP3-33111) 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/nbp3-33111_rabbit-zeb1-mab-je57-64-29820241492615.jpg)
![Western Blot: 2B4/CD244/SLAMF4 Antibody (025) [NBP2-89232] - Lane A: Daudi Whole Cell Lysate Lysates/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:42 kDa Observed band size:28 kDa (We are unsure as to the identity of these extra bands.)](http://images.novusbio.com/fullsize/2B4-CD244-SLAMF4-Antibody-025-Western-Blot-NBP2-89232-img0001.jpg "Western Blot: 2B4/CD244/SLAMF4 Antibody (025) [NBP2-89232] - Lane A: Daudi Whole Cell Lysate Lysates/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:42 kDa Observed band size:28 kDa (We are unsure as to the identity of these extra bands.)")
![Immunoprecipitation: 2B4/CD244/SLAMF4 Antibody (025) [NBP2-89232] - Lane A:0.5 mg Daudi Whole Cell Lysate 2 uL anti-2B4 rabbit monoclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-2B4 rabbit monoclonal antibody,at 1:200 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: 42 kDa Observed band size: 28 kDa](http://images.novusbio.com/fullsize/2B4-CD244-SLAMF4-Antibody-025-Immunoprecipitation-NBP2-89232-img0002.jpg)
![Western Blot: FAT10 Antibody [NBP2-99524] - Anti-FAT10 rabbit polyclonal antibody at 1:500 dilution. Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 25 kDa](http://images.novusbio.com/fullsize/FAT10-Antibody-Western-Blot-NBP2-99524-img0003.jpg "Western Blot: FAT10 Antibody [NBP2-99524] - Anti-FAT10 rabbit polyclonal antibody at 1:500 dilution. Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 25 kDa")
![Immunocytochemistry/Immunofluorescence: FAT10 Antibody [NBP2-99524] - Immunofluorescence staining of FAT10 in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-99524 antibody (dilution ratio 1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus .](http://images.novusbio.com/fullsize/nbp2-99524_rabbit-polyclonal-fat10-antibody-23520251628192.png)
![Western Blot: RIPK3/RIP3 Antibody (PSH04-79) [NBP3-32906] - Western blot analysis of RIPK3/RIP3 on different lysates with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32906) at 1/2,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HT-29 cell lysate Lane 3: SK-Br-3 cell lysate Lane 4: HeLa cell lysate (negative) Lysates/proteins at 30 ug/Lane. Predicted band size: 57 kDa Observed band size: 55 kDa Exposure time: 1 minute; ECL; 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 (NBP3-32906) 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/nbp3-32906_rabbit-ripk3-rip3-mab-psh04-79-288202412461630.jpg "Western Blot: RIPK3/RIP3 Antibody (PSH04-79) [NBP3-32906] - Western blot analysis of RIPK3/RIP3 on different lysates with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32906) at 1/2,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HT-29 cell lysate Lane 3: SK-Br-3 cell lysate Lane 4: HeLa cell lysate (negative) Lysates/proteins at 30 ug/Lane. Predicted band size: 57 kDa Observed band size: 55 kDa Exposure time: 1 minute; ECL; 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 (NBP3-32906) 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.")
![Immunohistochemistry: RIPK3/RIP3 Antibody (PSH04-79) [NBP3-32906] - Immunohistochemical analysis of paraffin-embedded HT-29 (positive) and HeLa (negative) cells with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32906) at 1/1,000 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 (NBP3-32906) at 1/1,000 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/nbp3-32906_rabbit-ripk3-rip3-mab-psh04-79-298202413585590.jpg)
![Immunohistochemistry-Paraffin: CHD4 Antibody [NBP2-99098] - Immunochemical staining of human CHD4 in human breast carcinoma with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/CHD4-Antibody-Immunohistochemistry-Paraffin-NBP2-99098-img0002.jpg "Immunohistochemistry-Paraffin: CHD4 Antibody [NBP2-99098] - Immunochemical staining of human CHD4 in human breast carcinoma with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).")
![Immunocytochemistry/Immunofluorescence: CHD4 Antibody [NBP2-99098] - Immunofluorescence staining of CHD4 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 NBP2-99098 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green).Positive staining was localized to nucleus.](http://images.novusbio.com/fullsize/nbp2-99098_rabbit-polyclonal-chd4-antibody-235202511444452.png)
![Western Blot: CHD4 Antibody [NBP2-99099] - Anti-CHD4 rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate Lane B: 293T Whole Cell Lysate Lane C: NIH3T3 Whole Cell Lysate Lane D: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 218 kDa](http://images.novusbio.com/fullsize/CHD4-Antibody-Western-Blot-NBP2-99099-img0002.jpg "Western Blot: CHD4 Antibody [NBP2-99099] - Anti-CHD4 rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate Lane B: 293T Whole Cell Lysate Lane C: NIH3T3 Whole Cell Lysate Lane D: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 218 kDa")
![Immunocytochemistry/Immunofluorescence: CHD4 Antibody [NBP2-99099] - Immunofluorescence staining of CHD4 in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-99099 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). Positive staining was localized to Nucleus.](http://images.novusbio.com/fullsize/nbp2-99099_rabbit-polyclonal-chd4-antibody-235202514371324.png)
![Immunohistochemistry-Paraffin: FKBP6 Antibody [NBP2-97729] - Immunochemical staining of human FKBP6 in human testis with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/FKBP6-Antibody-Immunohistochemistry-Paraffin-NBP2-97729-img0002.jpg "Immunohistochemistry-Paraffin: FKBP6 Antibody [NBP2-97729] - Immunochemical staining of human FKBP6 in human testis with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.")
![Immunocytochemistry/Immunofluorescence: FKBP6 Antibody [NBP2-97729] - Immunofluorescence staining of FKBP6 in A431 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-97729 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/nbp2-97729_rabbit-polyclonal-fkbp6-antibody-23520251628187.png)
![Immunohistochemistry-Paraffin: CD46 Antibody (001) [NBP2-90080] - Staining of human CD46 in human placenta with rabbit monoclonal antibody (1:200). Positive staining was localized to membrane of trophoblast.](http://images.novusbio.com/fullsize/CD46-Antibody-001-Immunohistochemistry-Paraffin-NBP2-90080-img0001.jpg "Immunohistochemistry-Paraffin: CD46 Antibody (001) [NBP2-90080] - Staining of human CD46 in human placenta with rabbit monoclonal antibody (1:200). Positive staining was localized to membrane of trophoblast.")
![Immunocytochemistry/Immunofluorescence: CD46 Antibody (001) [NBP2-90080] - Staining of CD46 in HepG2 cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-90080 antibody (1:60) at 4? overnight. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp2-90080_rabbit-monoclonal-cd46-antibody-001-235202514492342.png)
![Western Blot: LAMP-2/CD107b Antibody (D3-D8-D3-R) [NBP3-32523] - Western blot analysis of LAMP-2/CD107b on different lysates with Mouse anti-LAMP-2/CD107b antibody (NBP3-32523) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: Jurkat cell lysate Lane 3: HepG2 cell lysate Lane 4: HUVEC cell lysate Lane 5: JAR cell lysate Lane 6: HEK-293 cell lysate Lane 7: THP-1 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 45 kDa Observed band size: 110 kDa Exposure time: 3 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 (NBP3-32523) 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/nbp3-32523_mouse-lamp-2-cd107b-mab-d3-d8-d3-r-278202416331251.jpg "Western Blot: LAMP-2/CD107b Antibody (D3-D8-D3-R) [NBP3-32523] - Western blot analysis of LAMP-2/CD107b on different lysates with Mouse anti-LAMP-2/CD107b antibody (NBP3-32523) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: Jurkat cell lysate Lane 3: HepG2 cell lysate Lane 4: HUVEC cell lysate Lane 5: JAR cell lysate Lane 6: HEK-293 cell lysate Lane 7: THP-1 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 45 kDa Observed band size: 110 kDa Exposure time: 3 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 (NBP3-32523) 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: LAMP-2/CD107b Antibody (D3-D8-D3-R) [NBP3-32523] - Immunohistochemical analysis of paraffin-embedded human kidney tissue with Mouse anti-LAMP-2/CD107b antibody (NBP3-32523) at 1/5,000 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 (NBP3-32523) at 1/5,000 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/nbp3-32523_mouse-lamp-2-cd107b-mab-d3-d8-d3-r-298202414304116.jpg)