| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-30989-25ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-98957-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97262-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99325-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99460-50ul | |||
![Western Blot: c-Myc Antibody (33) [NBP3-30989] - Immunohistochemical staining of normal kidney tissue section using c-Myc antibody, clone 33 (Cat. No. NBP3-30989) at 10 ug/ml.](http://images.novusbio.com/fullsize/nbp3-30989_mouse-c-myc-mab-33-811202420592196.jpg "Western Blot: c-Myc Antibody (33) [NBP3-30989] - Immunohistochemical staining of normal kidney tissue section using c-Myc antibody, clone 33 (Cat. No. NBP3-30989) at 10 ug/ml.")
![Flow Cytometry: ErbB2/Her2 Antibody (24D2) [NBP3-09136] - Separation of MCF-7 cells stained using anti-human CD340 (24D2) purified antibody (concentration in sample 5,0 ug/ml, GAM APC, red-filled) from MCF-7 cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (surface staining).](http://images.novusbio.com/fullsize/ErbB2-Her2-Antibody-24D2-Flow-Cytometry-NBP3-09136-img0001.jpg "Flow Cytometry: ErbB2/Her2 Antibody (24D2) [NBP3-09136] - Separation of MCF-7 cells stained using anti-human CD340 (24D2) purified antibody (concentration in sample 5,0 ug/ml, GAM APC, red-filled) from MCF-7 cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (surface staining).")
![Immunohistochemistry: MAGEA1 Antibody (PD00-50) [NBP3-32559] - Immunohistochemical analysis of paraffin-embedded human malignant melanoma tissue with Rabbit anti-MAGEA1 antibody (NBP3-32559) at 1/1,500 dilution.<br/><br/> 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 (NBP3-32559) at 1/1,500 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/nbp3-32559_rabbit-magea1-mab-pd00-50-29820241420971.jpg "Immunohistochemistry: MAGEA1 Antibody (PD00-50) [NBP3-32559] - Immunohistochemical analysis of paraffin-embedded human malignant melanoma tissue with Rabbit anti-MAGEA1 antibody (NBP3-32559) at 1/1,500 dilution.<br/><br/> 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 (NBP3-32559) at 1/1,500 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.")
![Western blot analysis of A431 cell lysates with NBP3-32559 at 1/1,000 dilution. Lysates/proteins at 20 µg/Lane. Predicted band size: 34 kDa Observed band size: 45 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. NBP3-32559 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/nbp3-32559_-western-blot-639204594551210597.jpg)
![Western Blot: Kv10.2 Antibody [NBP2-83132] - WB Suggested Anti-KCNH5 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:312500. Positive Control: HepG2 cell lysate](http://images.novusbio.com/fullsize/Kv10.2-Antibody-Western-Blot-NBP2-83132-img0002.jpg "Western Blot: Kv10.2 Antibody [NBP2-83132] - WB Suggested Anti-KCNH5 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:312500. Positive Control: HepG2 cell lysate")
![Immunohistochemistry: Kv10.2 Antibody [NBP2-83132] - Human Brain](http://images.novusbio.com/fullsize/Kv10.2-Antibody-Immunohistochemistry-NBP2-83132-img0001.jpg)
![Western Blot: XRCC2 Antibody [NBP2-98957] - Anti-XRCC2 rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa 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: 32 kDa. Observed band size: 32 kDa](http://images.novusbio.com/fullsize/XRCC2-Antibody-Western-Blot-NBP2-98957-img0002.jpg "Western Blot: XRCC2 Antibody [NBP2-98957] - Anti-XRCC2 rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa 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: 32 kDa. Observed band size: 32 kDa")
![Immunocytochemistry/Immunofluorescence: XRCC2 Antibody [NBP2-98957] - Immunofluorescence staining of XRCC2 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 NBP2-98957 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/nbp2-98957_rabbit-polyclonal-xrcc2-antibody-235202511494015.png)
![Immunohistochemistry-Paraffin: ATG16L1 Antibody [NBP3-14543] - Human Brain, Cerebellum: Formalin-Fixed, Paraffin-Embedded (FFPE)](http://images.novusbio.com/fullsize/ATG16L1 Antibody-Immunohistochemistry-Paraffin-NBP3-14543-img0002.jpg "Immunohistochemistry-Paraffin: ATG16L1 Antibody [NBP3-14543] - Human Brain, Cerebellum: Formalin-Fixed, Paraffin-Embedded (FFPE)")
![Simple Western: ATG16L1 Antibody [NBP3-14543] - ATG16L1 antibody (LS-A11356, 20 mg/mL) yields a specific band on capillary Western analysis (Protein Simple, WES 12-230 kDa separation module) in 10 ng purified recombinant human ATG16L1 protein.](http://images.novusbio.com/fullsize/ATG16L1-Antibody-Simple-Western-NBP3-14543-img0001.jpg)
![Immunohistochemistry: TRPM8 Antibody (JE32-58) [NBP3-33062] - Immunohistochemical analysis of paraffin-embedded human liver cancer tissue with Rabbit anti-TRPM8 antibody (NBP3-33062) at 1/500 dilution.<br/><br/> 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 (NBP3-33062) at 1/500 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/nbp3-33062_rabbit-trpm8-mab-je32-58-298202414262669.jpg "Immunohistochemistry: TRPM8 Antibody (JE32-58) [NBP3-33062] - Immunohistochemical analysis of paraffin-embedded human liver cancer tissue with Rabbit anti-TRPM8 antibody (NBP3-33062) at 1/500 dilution.<br/><br/> 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 (NBP3-33062) at 1/500 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.")
![Western blot analysis on different lysates with NBP3-33062 at 1/1,000 dilution. Lane 1: LNCaP cell lysate Lane 2: MCF7 cell lysate Lane 3: HCT 116 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 128 kDa Observed band size: 110 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. NBP3-33062 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/nbp3-33062_-western-blot-639204597145868024.jpg)
![Western Blot: NF2/Merlin Antibody (JE31-02) [NBP3-32589] - Western blot analysis of NF2/Merlin on different lysates with Rabbit anti-NF2/Merlin antibody (NBP3-32589) at 1/500 dilution.<br/><br/> Lane 1: Hela cell lysate (10 ug/Lane)<br/> Lane 2: Mouse brain tissue lysate (20 ug/Lane)<br/> Lane 3: Rat brain tissue lysate (20 ug/Lane)<br/><br/> Predicted band size: 70 kDa<br/> Observed band size: 70 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 8% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32589) 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/nbp3-32589_rabbit-nf2-merlin-mab-je31-02-27820241631649.jpg "Western Blot: NF2/Merlin Antibody (JE31-02) [NBP3-32589] - Western blot analysis of NF2/Merlin on different lysates with Rabbit anti-NF2/Merlin antibody (NBP3-32589) at 1/500 dilution.<br/><br/> Lane 1: Hela cell lysate (10 ug/Lane)<br/> Lane 2: Mouse brain tissue lysate (20 ug/Lane)<br/> Lane 3: Rat brain tissue lysate (20 ug/Lane)<br/><br/> Predicted band size: 70 kDa<br/> Observed band size: 70 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 8% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32589) 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.")
![Western blot analysis on different lysates with NBP3-32589 at 1/5,000 dilution. Lane 1: HeLa (Human cervical adenocarcinoma cell) cell lysate Lane 2: Mouse brain tissue lysate Lysates/proteins at 25 µg/Lane. Exposure time: 59 Seconds Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: NBP3-32589, 1/5,000 in primary antibody dilution buffer, overnight at 4 ℃ Secondary antibody: Goat Anti-Rabbit IgG [HRP] Secondary Antibody, 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 70 kDa Observed band size: 70 kDa](http://images.novusbio.com/fullsize/nbp3-32589_-western-blot-639204597795357878.jpg)
![Western Blot: MTA2 Antibody [NBP2-87852] - WB Suggested Anti-MTA2 Antibody Titration: 1.25ug/ml. Positive Control: Jurkat cell lysateMTA2 is supported by BioGPS gene expression data to be expressed in Jurkat](http://images.novusbio.com/fullsize/MTA2-Antibody-Western-Blot-NBP2-87852-img0002.jpg "Western Blot: MTA2 Antibody [NBP2-87852] - WB Suggested Anti-MTA2 Antibody Titration: 1.25ug/ml. Positive Control: Jurkat cell lysateMTA2 is supported by BioGPS gene expression data to be expressed in Jurkat")
![Immunohistochemistry: MTA2 Antibody [NBP2-87852] - Human kidney](http://images.novusbio.com/fullsize/MTA2-Antibody-Immunohistochemistry-NBP2-87852-img0001.jpg)
![Immunohistochemistry-Paraffin: Bmf Antibody [NBP2-97262] - Immunochemical staining of human Bmf in human brain with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/Bmf-Antibody-Immunohistochemistry-Paraffin-NBP2-97262-img0002.jpg "Immunohistochemistry-Paraffin: Bmf Antibody [NBP2-97262] - Immunochemical staining of human Bmf in human brain with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.")
![Immunocytochemistry/Immunofluorescence: Bmf Antibody [NBP2-97262] - Immunofluorescence staining of Bmf 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 NBP2-97262 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 and Cytoplasm.](http://images.novusbio.com/fullsize/nbp2-97262_rabbit-polyclonal-bmf-antibody-23520251135416.png)
![Western Blot: Profilin 1 Antibody [NBP2-99325] - Lane A: HeLa Whole Cell LysateLane B: HepG2 Whole Cell LysateLane C: MCF7 Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:15 kDaObserved band size:15 kDa](http://images.novusbio.com/fullsize/Profilin-1-Antibody-Western-Blot-NBP2-99325-img0002.jpg "Western Blot: Profilin 1 Antibody [NBP2-99325] - Lane A: HeLa Whole Cell LysateLane B: HepG2 Whole Cell LysateLane C: MCF7 Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:15 kDaObserved band size:15 kDa")
![Immunocytochemistry/Immunofluorescence: Profilin 1 Antibody [NBP2-99325] - Immunofluorescence staining of Profilin 1 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 NBP2-99325 antibody (dilution ratio 1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor$488-conjugated Goat Anti-rabbit IgG Secondary antibody (green). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-99325_rabbit-polyclonal-profilin-1-antibody-235202511545629.png)
![Western Blot: Bmf Antibody [NBP2-99460] - Anti-Bmf rabbit polyclonal antibody at 1:500 dilution. Lane A: Hela 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: 20 kDa. Observed band size: 20 kDa](http://images.novusbio.com/fullsize/Bmf-Antibody-Western-Blot-NBP2-99460-img0003.jpg "Western Blot: Bmf Antibody [NBP2-99460] - Anti-Bmf rabbit polyclonal antibody at 1:500 dilution. Lane A: Hela 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: 20 kDa. Observed band size: 20 kDa")
![Immunocytochemistry/Immunofluorescence: Bmf Antibody [NBP2-99460] - Immunofluorescence staining of Bmf 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 NBP2-99460 antibody (dilution ratio 1:5000) 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 cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-99460_rabbit-polyclonal-bmf-antibody-235202511545650.png)