Note: Mouseover a species abbreviation on the product page to display the fullname.
How can we help you?
![Western Blot: HAND1 Antibody (8E7A11) [NBP1-51547] - Western blot analysis using HAND1 mouse mAb against truncated Trx-HAND1 recombinant protein (1).](http://images.novusbio.com/fullsize/HAND1-Antibody-8E7A11-Western-Blot-NBP1-51547-img0001.jpg "Western Blot: HAND1 Antibody (8E7A11) [NBP1-51547] - Western blot analysis using HAND1 mouse mAb against truncated Trx-HAND1 recombinant protein (1).")
![Flow Cytometry: CD45 Antibody (F10-89-4) [NBP1-28509] -Human peripheral blood lymphocytes were stained with mouse anti- human.](http://images.novusbio.com/fullsize/antibody/nbp1-28509_mouse-monoclonal-cd45-antibody-f10-89-4-flow-cytometry-1322024115231..jpg "Flow Cytometry: CD45 Antibody (F10-89-4) [NBP1-28509] -Human peripheral blood lymphocytes were stained with mouse anti- human.")
![Western Blot: Dynamin [p Ser774] Antibody [NB300-209] - Rat hippocampal lysate stimulated with forskolin showing specific immunolabeling of the ~95k dynamin phosphorylated at Ser774 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambda-Ptase). The blot is identical to the control except that it was incubated in lambda-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser774 dynamin. The immunolabeling is completely eliminated by treatment with lambda-Ptase.](http://images.novusbio.com/fullsize/Dynamin-[p-Ser774]-Antibody-Western-Blot-NB300-209-img0002.jpg "Western Blot: Dynamin [p Ser774] Antibody [NB300-209] - Rat hippocampal lysate stimulated with forskolin showing specific immunolabeling of the ~95k dynamin phosphorylated at Ser774 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambda-Ptase). The blot is identical to the control except that it was incubated in lambda-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser774 dynamin. The immunolabeling is completely eliminated by treatment with lambda-Ptase.")
![Western Blot: Josephin1 Antibody (OTI3B11) - Azide and BSA Free [NBP2-71506] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Josephin1 (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-Josephin1.](http://images.novusbio.com/fullsize/Josephin1-Antibody-OTI3B11-Azide-and-BSA-Free-Western-Blot-NBP2-71506-img0001.jpg "Western Blot: Josephin1 Antibody (OTI3B11) - Azide and BSA Free [NBP2-71506] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Josephin1 (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-Josephin1.")
![Immunohistochemistry: Josephin1 Antibody (OTI3B11) - Azide and BSA Free [NBP2-71506] - Staining of paraffin-embedded Human prostate tissue using anti-Josephin1 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/Josephin1-Antibody-OTI3B11-Azide-and-BSA-Free-Immunohistochemistry-NBP2-71506-img0002.jpg)
![Western Blot: FUNDC1 Antibody (PSH0-92) [NBP3-32353] - Western blot analysis of FUNDC1 on different lysates with Rabbit anti-FUNDC1 antibody (NBP3-32353) at 1/1,000 dilution. Lane 1: 293T over-expressed FUNDC1 cell lysate Lane 2: 293T control cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 17 kDa Observed band size: 17 kDa Exposure time: 2 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 (NBP3-32353) 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 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32353_rabbit-fundc1-mab-psh0-92-278202415212473.jpg "Western Blot: FUNDC1 Antibody (PSH0-92) [NBP3-32353] - Western blot analysis of FUNDC1 on different lysates with Rabbit anti-FUNDC1 antibody (NBP3-32353) at 1/1,000 dilution. Lane 1: 293T over-expressed FUNDC1 cell lysate Lane 2: 293T control cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 17 kDa Observed band size: 17 kDa Exposure time: 2 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 (NBP3-32353) 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 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: FUNDC1 Antibody (PSH0-92) [NBP3-32353] - Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-FUNDC1 antibody (NBP3-32353) at 1/50 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 (NBP3-32353) at 1/50 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/nbp3-32353_rabbit-fundc1-mab-psh0-92-298202414304167.jpg)
![Western Blot: CPN1 Antibody [NBP3-32212] - Western blot analysis of CPN1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32212, 1/500) 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. Positive control: Lane 1: Hela cell lysate Lane 2: Raji cell lysate Lane 3: Mouse pancreas tissue lysate Predicted band size: 52 kDa Observed band size: 55 kDa](http://images.novusbio.com/fullsize/nbp3-32212_rabbit-cpn1-pab-27820241631630.jpg "Western Blot: CPN1 Antibody [NBP3-32212] - Western blot analysis of CPN1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32212, 1/500) 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. Positive control: Lane 1: Hela cell lysate Lane 2: Raji cell lysate Lane 3: Mouse pancreas tissue lysate Predicted band size: 52 kDa Observed band size: 55 kDa")
![Immunocytochemistry/ Immunofluorescence: CPN1 Antibody [NBP3-32212] - ICC staining of CPN1 in LOVO cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP3-32212, 1/100) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32212_rabbit-cpn1-pab-29202410334058.jpg)
![Immunocytochemistry/Immunofluorescence: Integrin alpha 2b/CD41 Antibody (IVA30) [NB500-496] - Immunocytochemistry staining of acetone/methanol fixed bovine peripheral blood (thrombocyte-enriched suspension) using anti-bovine CD41/CD61 (IVA30); secondary antibody conjugated to FITC (green signal at thrombocytes), DNA stained with DAPI (blue signal).](http://images.novusbio.com/fullsize/Integrin-alpha-2b-CD41-Antibody-IVA30-Immunocytochemistry-Immunofluorescence-NB500-496-img0001.jpg "Immunocytochemistry/Immunofluorescence: Integrin alpha 2b/CD41 Antibody (IVA30) [NB500-496] - Immunocytochemistry staining of acetone/methanol fixed bovine peripheral blood (thrombocyte-enriched suspension) using anti-bovine CD41/CD61 (IVA30); secondary antibody conjugated to FITC (green signal at thrombocytes), DNA stained with DAPI (blue signal).")
![Western Blot: RIPK3/RIP3 [p Ser232] Antibody (JE44-62) [NBP3-32795] - Western blot analysis of RIPK3/RIP3 on different lysates with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32795) at 1/1,000 dilution. Lane 1: L-929 whole cell lysate Lane 2: L-929 treated with 20uM Z-VAD for 3.5 hours, add 100nM SM-164 and 20ng/ml TNF-a for 3 hours whole cell lysate Lane 3: L-929 treated with pp for 1 hour whole cell lysate Lane 4: L-929 treated with 20uM Z-VAD for 3.5 hours, add 100nM SM-164 and 20ng/ml TNF-a for 3 hours, treated with pp for 1 hour whole cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 53 kDa Observed band size: 53 kDa Exposure time: 20 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 (NBP3-32795) 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 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32795_rabbit-ripk3-rip3-p-ser232-mab-je44-62-288202412442911.jpg "Western Blot: RIPK3/RIP3 [p Ser232] Antibody (JE44-62) [NBP3-32795] - Western blot analysis of RIPK3/RIP3 on different lysates with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32795) at 1/1,000 dilution. Lane 1: L-929 whole cell lysate Lane 2: L-929 treated with 20uM Z-VAD for 3.5 hours, add 100nM SM-164 and 20ng/ml TNF-a for 3 hours whole cell lysate Lane 3: L-929 treated with pp for 1 hour whole cell lysate Lane 4: L-929 treated with 20uM Z-VAD for 3.5 hours, add 100nM SM-164 and 20ng/ml TNF-a for 3 hours, treated with pp for 1 hour whole cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 53 kDa Observed band size: 53 kDa Exposure time: 20 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 (NBP3-32795) 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 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: RIPK3/RIP3 [p Ser232] Antibody (JE44-62) [NBP3-32795] - Immunocytochemistry analysis of L-929 cells treated with or without 20μM Z-VAD for 2.75 hours, add 100nM SM-164 and 20ng/ml TNF-alpha for 2.25 hours, then treated with lambda pp for 1 hour labeling RIPK3/RIP3 with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32795) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-RIPK3/RIP3 antibody (NBP3-32795) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. 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/nbp3-32795_rabbit-ripk3-rip3-p-ser232-mab-je44-62-29202410234210.jpg)
![Western Blot: Cofilin Antibody (PSH0-34) [NBP3-32205] - Western blot analysis of Cofilin on different lysates with Rabbit anti-Cofilin antibody (NBP3-32205) at 1/1,000 dilution. Lane 1: Hela cell lysate (30 ug/Lane) Lane 2: HEK-293 cell lysate (30 ug/Lane) Lane 3: MCF-7 cell lysate (30 ug/Lane) Lane 4: MDA-MB-468 cell lysate (24 ug/Lane) Lane 5: K-562 cell lysate (16 ug/Lane) Lane 6: SH-SY5Y cell lysate (22 ug/Lane) Lane 7: HUVEC cell lysate (30 ug/Lane) Lane 8: Jurkat cell lysate (30 ug/Lane) Lane 9: COS-1 cell lysate (30 ug/Lane) Lane 10: VERO cell lysate (30 ug/Lane) Lane 11: NIH/3T3 cell lysate (22 ug/Lane) Lane 12: PC-12 cell lysate (19 ug/Lane) Lane 13: Neuro-2a cell lysate (19 ug/Lane) Predicted band size: 19 kDa Observed band size: 19 kDa Exposure time: 3 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 (NBP3-32205) 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 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32205_rabbit-cofilin-mab-psh0-34-278202415295596.jpg "Western Blot: Cofilin Antibody (PSH0-34) [NBP3-32205] - Western blot analysis of Cofilin on different lysates with Rabbit anti-Cofilin antibody (NBP3-32205) at 1/1,000 dilution. Lane 1: Hela cell lysate (30 ug/Lane) Lane 2: HEK-293 cell lysate (30 ug/Lane) Lane 3: MCF-7 cell lysate (30 ug/Lane) Lane 4: MDA-MB-468 cell lysate (24 ug/Lane) Lane 5: K-562 cell lysate (16 ug/Lane) Lane 6: SH-SY5Y cell lysate (22 ug/Lane) Lane 7: HUVEC cell lysate (30 ug/Lane) Lane 8: Jurkat cell lysate (30 ug/Lane) Lane 9: COS-1 cell lysate (30 ug/Lane) Lane 10: VERO cell lysate (30 ug/Lane) Lane 11: NIH/3T3 cell lysate (22 ug/Lane) Lane 12: PC-12 cell lysate (19 ug/Lane) Lane 13: Neuro-2a cell lysate (19 ug/Lane) Predicted band size: 19 kDa Observed band size: 19 kDa Exposure time: 3 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 (NBP3-32205) 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 1:200,000 dilution was used for 1 hour at room temperature.")
![Flow Cytometry: Cofilin Antibody (PSH0-34) [NBP3-32205] - Flow cytometric analysis of Hela cells labeling Cofilin. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32205, 1ug/ml) (red) compared with Rabbit IgG 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-Rabbit 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/nbp3-32205_rabbit-cofilin-mab-psh0-34-29202416453265.jpg)
![Western Blot: CD14 Antibody (PD01-63) [NBP3-32125] - Western blot analysis of CD14 on different lysates with Rabbit anti-CD14 antibody (NBP3-32125) at 1/1,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: SiHa cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 40 kDa Observed band size: 60 kDa Exposure time: 2 minutes; 8% 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 (NBP3-32125) 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 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32125_rabbit-cd14-mab-pd01-63-278202416285230.jpg "Western Blot: CD14 Antibody (PD01-63) [NBP3-32125] - Western blot analysis of CD14 on different lysates with Rabbit anti-CD14 antibody (NBP3-32125) at 1/1,000 dilution. Lane 1: NIH/3T3 cell lysate Lane 2: SiHa cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 40 kDa Observed band size: 60 kDa Exposure time: 2 minutes; 8% 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 (NBP3-32125) 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 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CD14 Antibody (PD01-63) [NBP3-32125] - Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue with Rabbit anti-CD14 antibody (NBP3-32125) 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 (NBP3-32125) 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/nbp3-32125_rabbit-cd14-mab-pd01-63-29820241492696.jpg)