| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97580-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-11923-25ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98731-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99542-50ul | |||
![Western Blot: Glut4 [p Ser488] Antibody (JE43-23) [NBP3-32766] - Western blot analysis of Glut4 on mouse heart tissue lysates (no heat) with Rabbit anti-Glut4 antibody (NBP3-32766) at 1/1,000 dilution. Lysates/proteins at 30 ug/Lane. Predicted band size: 55 kDa Observed band size: 50 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 (NBP3-32766) at 1/1,000 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/nbp3-32766_rabbit-glut4-p-ser488-mab-je43-23-288202412442949.jpg "Western Blot: Glut4 [p Ser488] Antibody (JE43-23) [NBP3-32766] - Western blot analysis of Glut4 on mouse heart tissue lysates (no heat) with Rabbit anti-Glut4 antibody (NBP3-32766) at 1/1,000 dilution. Lysates/proteins at 30 ug/Lane. Predicted band size: 55 kDa Observed band size: 50 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 (NBP3-32766) at 1/1,000 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-Paraffin: alpha-1D Adrenergic R/ADRA1D Antibody [NBP2-97580] - Immunochemical staining of human alpha-1D Adrenergic R/ADRA1D in human kidney with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/alpha-1D-Adrenergic-R-ADRA1D-Antibody-Immunohistochemistry-Paraffin-NBP2-97580-img0001.jpg "Immunohistochemistry-Paraffin: alpha-1D Adrenergic R/ADRA1D Antibody [NBP2-97580] - Immunochemical staining of human alpha-1D Adrenergic R/ADRA1D in human kidney with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: alpha-1D Adrenergic R/alpha-1D Adrenergic R/ADRA1D Antibody - BSA Free [NBP2-97580] - Immunochemical staining of human alpha-1D Adrenergic R/ADRA1D in human kidney with NBP2-97580 at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp2-97580_rabbit-polyclonal-alpha-1d-adrenergic-r-adra1d-antibody-23520252135141.png)
![Immunohistochemistry: CACNA1G Antibody [NBP3-11923] - Immunohistochemical staining of human melanoma tumor tissue using CACNA1G antibody at 15 ug/ml.](http://images.novusbio.com/fullsize/CACNA1G-Antibody-Immunohistochemistry-NBP3-11923-img0001.jpg "Immunohistochemistry: CACNA1G Antibody [NBP3-11923] - Immunohistochemical staining of human melanoma tumor tissue using CACNA1G antibody at 15 ug/ml.")
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody (JE63-95) [NBP3-33135] - Western blot analysis of Acetyl-CoA Carboxylase alpha/ACACA on different lysates with Rabbit anti-Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-33135) at 1/2,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes cell lysate Lane 3: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes then treated with pp for 1 hour cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 265 kDa Observed band size: 265 kDa Exposure time: 1 minutes 14 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 (NBP3-33135) 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/nbp3-33135_rabbit-acetyl-coa-carboxylase-alpha-acaca-p-ser79-mab-28820241423319.jpg "Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody (JE63-95) [NBP3-33135] - Western blot analysis of Acetyl-CoA Carboxylase alpha/ACACA on different lysates with Rabbit anti-Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-33135) at 1/2,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes cell lysate Lane 3: NIH/3T3 treated with 0.5uM Oligomycin for 30 minutes then treated with pp for 1 hour cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 265 kDa Observed band size: 265 kDa Exposure time: 1 minutes 14 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 (NBP3-33135) 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-Paraffin: Caveolin-2 Antibody [NBP2-98731] - Staining of human Caveolin-2 in human corpus uteri with rabbit polyclonal antibody (1:1000).](http://images.novusbio.com/fullsize/Caveolin-2-Antibody-Immunohistochemistry-Paraffin-NBP2-98731-img0002.jpg "Immunohistochemistry-Paraffin: Caveolin-2 Antibody [NBP2-98731] - Staining of human Caveolin-2 in human corpus uteri with rabbit polyclonal antibody (1:1000).")
![Immunohistochemistry-Paraffin: Caveolin-2 Antibody [NBP2-98731] - Staining of human Caveolin-2 in human cervix uteri with rabbit polyclonal antibody (1:1000).](http://images.novusbio.com/fullsize/Caveolin-2-Antibody-Immunohistochemistry-Paraffin-NBP2-98731-img0001.jpg)
![Western Blot: Caveolin-2 Antibody [NBP2-99542] - Anti-Caveolin-2 rabbit polyclonal antibody at 1:1000 dilution. Lane A: Mouse lung tissue 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: 24 kDa (We are unsure as to the identity of these extra bands).x](http://images.novusbio.com/fullsize/Caveolin-2-Antibody-Western-Blot-NBP2-99542-img0004.jpg "Western Blot: Caveolin-2 Antibody [NBP2-99542] - Anti-Caveolin-2 rabbit polyclonal antibody at 1:1000 dilution. Lane A: Mouse lung tissue 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: 24 kDa (We are unsure as to the identity of these extra bands).x")
![Immunoprecipitation: Caveolin-2 Antibody [NBP2-99542] - Caveolin-2 was immunoprecipitated using: Lane A: 0.5 mg Mouse lung tissue Lysate 4 ul anti-Caveolin-2 rabbit polyclonal antibody and 60 ug of Immunomagnetic beads. Protein A/G. Primary antibody: Anti-Caveolin-2 rabbit polyclonal antibody, at 1:100 dilution. Secondary antibody: 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: 22 kDa](http://images.novusbio.com/fullsize/Caveolin-2-Antibody-Immunoprecipitation-NBP2-99542-img0003.jpg)
![Western Blot: KCNK4 Antibody (13E9) - Chimeric - BSA Free [NBP3-43571] - Kelly cells lysate (35ug protein in RIPA buffer) was resolved via SDS-PAGE, and the subsequent blot was probed with NBP3-43571 at 1ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and proteins were detected by chemiluminescence.](http://images.novusbio.com/fullsize/nbp3-43571_rabbit-kcnk4-mab-13e9-chimeric-azide-and-bsa-free-7420252226521.png "Western Blot: KCNK4 Antibody (13E9) - Chimeric - BSA Free [NBP3-43571] - Kelly cells lysate (35ug protein in RIPA buffer) was resolved via SDS-PAGE, and the subsequent blot was probed with NBP3-43571 at 1ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and proteins were detected by chemiluminescence.")
![Immunocytochemistry /Immunofluorescence: KCNK4 Antibody (13E9) - Chimeric - BSA Free [NBP3-43571] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on Shi-fix coverslips stained with NBP3-43571 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43571, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43571_rabbit-kcnk4-mab-13e9-chimeric-azide-and-bsa-free-7420252211309.png)
![Immunocytochemistry/ Immunofluorescence: KCNK4 Antibody (13E9) - BSA Free [NBP3-43541] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on coverslips stained with NBP3-43541 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43541, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43541_mouse-kcnk4-mab-13e9-azide-and-bsa-free-immunocytochemistry-immunofluorescence-2220260333119.png "Immunocytochemistry/ Immunofluorescence: KCNK4 Antibody (13E9) - BSA Free [NBP3-43541] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on coverslips stained with NBP3-43541 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43541, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.")
![Western Blot: KCNK4 Antibody (13E9) - BSA Free [NBP3-43541] - Kelly cells lysate (35µg protein in RIPA buffer) was resolved via SDS-PAGE, and the subsequent blot was probed with NBP3-43541 at 1µg/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and proteins were detected by chemiluminescence.](http://images.novusbio.com/fullsize/nbp3-43541_mouse-kcnk4-mab-13e9-azide-and-bsa-free-western-blot-222026033318.png)
![Western Blot: S100A/B Antibody (C10) [NBP3-41554] - Sample: Lane1: HT1080 cell lysate; Lane2: HepG2 cell lysate Primary Ab: 0.2ug/ml NBP3-41554; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41554_mouse-s100a-b-mab-c10-612202421304347.jpg "Western Blot: S100A/B Antibody (C10) [NBP3-41554] - Sample: Lane1: HT1080 cell lysate; Lane2: HepG2 cell lysate Primary Ab: 0.2ug/ml NBP3-41554; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: S100A/B Antibody (C5) [NBP3-41222] - Sample: Lane1: HT1080 cell lysate; Lane2: HepG2 cell lysate Primary Ab: 0.2ug/ml NBP3-41222; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41222_mouse-s100a-b-mab-c5-61220242116271.jpg "Western Blot: S100A/B Antibody (C5) [NBP3-41222] - Sample: Lane1: HT1080 cell lysate; Lane2: HepG2 cell lysate Primary Ab: 0.2ug/ml NBP3-41222; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: S100A/B Antibody (C5) [NBP3-41222] - Sample: Lane1: HT1080 cell lysate; Lane2: HepG2 cell lysate Primary Ab: 0.2ug/ml NBP3-41222; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41222_mouse-s100a-b-mab-c5-612202421243244.jpg)