| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26422-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26542-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21576-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-76621-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-74485 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-02995-20ul | |||
![Immunohistochemistry-Paraffin: TDO2 Antibody (C2) [NBP3-41854] - DAB staining on IHC-P; Sample: Human Liver Tissue; Primary Ab: 10ug/ml NBP3-41854; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41854_mouse-tdo2-mab-c2-61220242126297.jpg "Immunohistochemistry-Paraffin: TDO2 Antibody (C2) [NBP3-41854] - DAB staining on IHC-P; Sample: Human Liver Tissue; Primary Ab: 10ug/ml NBP3-41854; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: TDO2 Antibody (C2) [NBP3-41854] - Sample: Lane1: Porcine Liver lysate; Lane2: Rat Liver lysate Primary Ab: 2ug/ml NBP3-41854; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41854_mouse-tdo2-mab-c2-612202421243225.jpg)
![Immunohistochemistry-Paraffin: TDO2 Antibody (C2) [NBP3-41854] - DAB staining on IHC-P; Sample: Human Skeletal muscle Tissue; Primary Ab: 10ug/ml NBP3-41854; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41854_mouse-tdo2-mab-c2-612202421121318.jpg)
![Immunohistochemistry: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Image of GSK-3 beta [p Ser9] Antibody (3A6) diluted at 1:100 and staining in paraffin-embedded human kidney tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26422_rabbit-gsk-3-beta-p-ser-9-mab-3a6-26220241525330.jpg "Immunohistochemistry: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Image of GSK-3 beta [p Ser9] Antibody (3A6) diluted at 1:100 and staining in paraffin-embedded human kidney tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Western Blot: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Positive Western Blot detected in Hela whole cell lysate, 293 whole cell lysate, A549 whole cell lysate (treated with Calyculin A or not). All lanes: GSK-3 beta [p Ser9] Antibody at 0.77ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 46 KDa Observed band size: 46 KDa](http://images.novusbio.com/fullsize/nbp3-26422_rabbit-gsk-3-beta-p-ser-9-mab-3a6-28220241136300.jpg)
![Immunocytochemistry/Immunofluorescence: GSK-3 beta [p Ser9] Antibody (3A6) [NBP3-26422] - Staining of Hela cells(treated with 50mM Calyculin A for 30min) with GSK-3 beta [p Ser9] Antibody (3A6) at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26422_rabbit-gsk-3-beta-p-ser-9-mab-3a6-28220241312216.jpg)
![Western Blot: PPME1 Antibody [NBP2-19903] - Sample (30 ug of whole cell lysate) A: NIH-3T3 B: JC 10% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/PPME1-Antibody-Western-Blot-NBP2-19903-img0002.jpg "Western Blot: PPME1 Antibody [NBP2-19903] - Sample (30 ug of whole cell lysate) A: NIH-3T3 B: JC 10% SDS PAGE gel, diluted at 1:1000.")
![Immunohistochemistry-Paraffin: PPME1 Antibody [NBP2-19903] - Immunohistochemical analysis of paraffin-embedded Hepatoma, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/PPME1-Antibody-Immunohistochemistry-Paraffin-NBP2-19903-img0003.jpg)
![Western Blot: PPME1 Antibody [NBP2-19903] - Sample (30 ug of whole cell lysate) A: 293T B: A431 C: HeLa D: HepG2 10% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/PPME1-Antibody-Western-Blot-NBP2-19903-img0001.jpg)
![Immunohistochemistry: GSK-3 beta Antibody (9G11) [NBP3-26542] - Image of GSK-3 beta Antibody (9G11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-262202414471519.jpg "Immunohistochemistry: GSK-3 beta Antibody (9G11) [NBP3-26542] - Image of GSK-3 beta Antibody (9G11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Western Blot: GSK-3 beta Antibody (9G11) [NBP3-26542] - Positive Western Blot detected in: Hela whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate, 293 whole cell lysate. All lanes: GSK3 beta Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 47, 49 kDa Observed band size: 47 kDa](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-28220241140910.jpg)
![Immunocytochemistry/Immunofluorescence: GSK-3 beta Antibody (9G11) [NBP3-26542] - Staining of Hela Cells with GSK-3 beta Antibody (9G11) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-282202412475130.jpg)
![Immunohistochemistry: GSK-3 beta [p Ser 9] Antibody (SR1801) [NBP3-21576] - Immunohistochemical analysis of paraffin-embedded human kidney, using NBP3-21576.](http://images.novusbio.com/fullsize/nbp3-21576_rabbit-gsk-3-beta-p-ser-9-mab-sr1801-5720231526118.jpg "Immunohistochemistry: GSK-3 beta [p Ser 9] Antibody (SR1801) [NBP3-21576] - Immunohistochemical analysis of paraffin-embedded human kidney, using NBP3-21576.")
![Immunocytochemistry/Immunofluorescence: GSK-3 beta [p Ser 9] Antibody (SR1801) [NBP3-21576] - Immunofluorescent analysis of HeLa cells treated with Calyculin A, using NBP3-21576.](http://images.novusbio.com/fullsize/nbp3-21576_rabbit-gsk-3-beta-p-ser-9-mab-sr1801-57202316494217.jpg)
![Western Blot: GSK-3 beta [p Ser 9] Antibody (SR1801) [NBP3-21576] - Western blot analysis using NBP3-21576 in 293T cell lysates, treated with Calyculin A.](http://images.novusbio.com/fullsize/nbp3-21576_rabbit-gsk-3-beta-p-ser-9-mab-sr1801-5720231754890.jpg)
![Western Blot: 4EBP1 Antibody [NBP1-76621] - eIF [NBP1-76621] - Analysis of eIF4EBP1 in human brain cell lysate with eIF4EBP1 antibody using NBP1-76621 at (A) 2.5, (B) 5 and (C) 10 ug/ml.](http://images.novusbio.com/fullsize/4EBP1-Antibody-Western-Blot-NBP1-76621-img0004.jpg "Western Blot: 4EBP1 Antibody [NBP1-76621] - eIF [NBP1-76621] - Analysis of eIF4EBP1 in human brain cell lysate with eIF4EBP1 antibody using NBP1-76621 at (A) 2.5, (B) 5 and (C) 10 ug/ml.")
![Immunocytochemistry/Immunofluorescence: 4EBP1 Antibody [NBP1-76621] - 3T3 cells with eIF4EBP1 antibody at 2 ug/ml.](http://images.novusbio.com/fullsize/4EBP1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-76621-img0002.jpg)
![Immunocytochemistry/ Immunofluorescence: 4EBP1 Antibody - BSA Free [NBP1-76621] - Immunofluorescence of 4EBP1 in 3T3 cells with 4EBP1 antibody at 20 ug/ml.Green: 4EBP1 Antibody Blue: DAPI staining](http://images.novusbio.com/fullsize/nbp1-76621_rabbit-polyclonal-4ebp1-antibody-2711202420285820.gif)
![Western Blot: IRS1 [p Ser307] Antibody [NBP1-78078] - Band at ~180 kDa believed to represent phosphorylated IRS1 (arrowhead). Lane 1 shows staining of human 293 cell lysate. Lane 2 shows staining of 293 cell lysate. The pronounced staining of the band at 180 kDa is not seen when the antibody was pre-incubated with immunizing peptide prior to reaction. The identity of the intensely reactive bands at ~70 kD in both lane 1 and 2 is unknown, although these bands were also competed out by pre-incubation with the immunizing peptide. (800 nm channel, green). Molecular weight estimation was made by comparison to prestained MW markers in lane M (700 nm channel, red).](http://images.novusbio.com/fullsize/IRS1-[p-Ser307]-Antibody-Western-Blot-NBP1-78078-img0001.jpg "Western Blot: IRS1 [p Ser307] Antibody [NBP1-78078] - Band at ~180 kDa believed to represent phosphorylated IRS1 (arrowhead). Lane 1 shows staining of human 293 cell lysate. Lane 2 shows staining of 293 cell lysate. The pronounced staining of the band at 180 kDa is not seen when the antibody was pre-incubated with immunizing peptide prior to reaction. The identity of the intensely reactive bands at ~70 kD in both lane 1 and 2 is unknown, although these bands were also competed out by pre-incubation with the immunizing peptide. (800 nm channel, green). Molecular weight estimation was made by comparison to prestained MW markers in lane M (700 nm channel, red).")
![Immunocytochemistry/Immunofluorescence: SHP-2/PTPN11 Antibody [NBP2-42920] - Analysis of Denque virus 2-infected BHK-21, using NS1 (Dengue virus) antibody at 1:2000 dilution.](http://images.novusbio.com/fullsize/SHP-2-PTPN11-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-42920-img0001.jpg "Immunocytochemistry/Immunofluorescence: SHP-2/PTPN11 Antibody [NBP2-42920] - Analysis of Denque virus 2-infected BHK-21, using NS1 (Dengue virus) antibody at 1:2000 dilution.")
![Immunohistochemistry-Paraffin: IRS1 Antibody [NBP2-16992] - Paraffin-embedded lung carcinoma. IRS1 antibody [C2C3], C-term dilution: 1:500.](http://images.novusbio.com/fullsize/IRS1-Antibody-Immunohistochemistry-Paraffin-NBP2-16992-img0004.jpg "Immunohistochemistry-Paraffin: IRS1 Antibody [NBP2-16992] - Paraffin-embedded lung carcinoma. IRS1 antibody [C2C3], C-term dilution: 1:500.")
![Western Blot: IRS1 Antibody [NBP2-16992] - Sample (30 ug of whole cell lysate) A: A431 5% SDS PAGE gel, diluted at 1:10000.](http://images.novusbio.com/fullsize/IRS1-Antibody-Western-Blot-NBP2-16992-img0001.jpg)
![Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with IRS1 antibody [C2C3], C-term (NBP2-16992) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-16992_rabbit-polyclonal-irs1-antibody-western-blot-2611202518375022.jpg)
![Western Blot: TDO2 Antibody (1D1) [NBP2-02002] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY TDO2 (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-TDO2.](http://images.novusbio.com/fullsize/TDO2-Antibody-1D1-Western-Blot-NBP2-02002-img0001.jpg "Western Blot: TDO2 Antibody (1D1) [NBP2-02002] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY TDO2 (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-TDO2.")
![Western Blot: 4EBP1 Antibody [NBP3-02995] - Analysis of extracts of various cell lines, using eIF4EBP1 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 Enhanced Kit. Exposure time: 300s.](http://images.novusbio.com/fullsize/4EBP1-Antibody-Western-Blot-NBP3-02995-img0004.jpg "Western Blot: 4EBP1 Antibody [NBP3-02995] - Analysis of extracts of various cell lines, using eIF4EBP1 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 Enhanced Kit. Exposure time: 300s.")
![Western Blot: TBC1D4 [p Thr642] Antibody (JE60-97) [NBP3-32749] - Western blot analysis of TBC1D4 on different lysates with Rabbit anti-TBC1D4 antibody (NBP3-32749) at 1/1,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: NIH/3T3 starve overnight then treated with 100nM Calyculin A for 50 minutes add 100ng/mL insulin for 20 minutes cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 147 kDa Observed band size: 160 kDa Exposure time: 25 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 (NBP3-32749) at 1/1,000 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/nbp3-32749_rabbit-tbc1d4-p-thr642-mab-je60-97-278202415212425.jpg "Western Blot: TBC1D4 [p Thr642] Antibody (JE60-97) [NBP3-32749] - Western blot analysis of TBC1D4 on different lysates with Rabbit anti-TBC1D4 antibody (NBP3-32749) at 1/1,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: NIH/3T3 starve overnight then treated with 100nM Calyculin A for 50 minutes add 100ng/mL insulin for 20 minutes cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 147 kDa Observed band size: 160 kDa Exposure time: 25 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 (NBP3-32749) at 1/1,000 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.")
![Immunocytochemistry/ Immunofluorescence: TBC1D4 [p Thr642] Antibody (JE60-97) [NBP3-32749] - Immunocytochemistry analysis of NIH/3T3 cells starved overnight then treated with or without 100nM Calyculin A for 50 minutes add 100ng/mL insulin for 20 minutes labeling TBC1D4 with Rabbit anti-TBC1D4 antibody (NBP3-32749) 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 Rabbit anti-TBC1D4 antibody (NBP3-32749) at 1/100 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/nbp3-32749_rabbit-tbc1d4-p-thr642-mab-je60-97-29202410484887.jpg)