| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47884-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47889-0.1mg | |||
| IHC-Prediluted | NBP2-48389 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21168-100ul | |||
| BSA Free | NBP3-21168-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-65366-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-35146-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-11784-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90271-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11978-0.025mg | |||
![Western Blot: MCPIP1/ZC3H12A Antibody (HL1442) - Azide and BSA Free [NBP3-25765] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ZC3H12A antibody [HL1442] (NBP3-25765) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-25765_rabbit-mcpip1-zc3h12a-mab-hl1442-azide-and-bsa-free-2120249413347.jpg "<b>Genetic Strategies Validation. </b>Western Blot: MCPIP1/ZC3H12A Antibody (HL1442) - Azide and BSA Free [NBP3-25765] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ZC3H12A antibody [HL1442] (NBP3-25765) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![<b>Genetic Strategies Validation. </b>Western Blot: MCPIP1/ZC3H12A Antibody (HL1442) - Azide and BSA Free [NBP3-25765] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 | 20 | 20 | 10 | 10 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ZC3H12A antibody [HL1442] (NBP3-25765) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25765_rabbit-mcpip1-zc3h12a-mab-hl1442-azide-and-bsa-free-2120249351328.jpg)
![Western Blot: MCPIP1/ZC3H12A Antibody (HL1442) - Azide and BSA Free [NBP3-25765] - Untreated (-) and treated (+) THP-1 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ZC3H12A antibody [HL1442] (NBP3-25765) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25765_rabbit-mcpip1-zc3h12a-mab-hl1442-azide-and-bsa-free-2120249432887.jpg)
![Western Blot: MCPIP1/ZC3H12A Antibody (HL1442) - Azide and BSA Free [NBP3-25765] - Whole cell extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with ZC3H12A antibody [HL1442] (NBP3-25765) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-25765_rabbit-mcpip1-zc3h12a-mab-hl1442-azide-and-bsa-free-212024939128.jpg)
![Immunohistochemistry-Paraffin: GFAP Antibody [NB120-16997] - Formalin fixed paraffin embedded human brain stained with GFAP antibody.](http://images.novusbio.com/fullsize/GFAP-Antibody-Immunohistochemistry-Paraffin-NB120-16997-img0002.jpg "Immunohistochemistry-Paraffin: GFAP Antibody [NB120-16997] - Formalin fixed paraffin embedded human brain stained with GFAP antibody.")
![Immunohistochemistry-Paraffin: GFAP Antibody [NB120-16997] - Formalin fixed paraffin embedded human astrocytoma stained with GFAP antibody.](http://images.novusbio.com/fullsize/GFAP-Antibody-Immunohistochemistry-Paraffin-NB120-16997-img0001.jpg)
![Immunohistochemistry-Paraffin: MUC1 Antibody (MUC1/955) - IHC-Prediluted [NBP2-48360] - Formalin-fixed, paraffin-embedded human Endometrial Carcinoma stained with MUC-1 / CA15-3 / EMA Mouse Monoclonal Antibody (MUC1/955).](http://images.novusbio.com/fullsize/MUC1-Antibody-MUC1-955-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48360-img0003.jpg "Immunohistochemistry-Paraffin: MUC1 Antibody (MUC1/955) - IHC-Prediluted [NBP2-48360] - Formalin-fixed, paraffin-embedded human Endometrial Carcinoma stained with MUC-1 / CA15-3 / EMA Mouse Monoclonal Antibody (MUC1/955).")
![Immunohistochemistry-Paraffin: MUC1 Antibody (MUC1/955) - IHC-Prediluted [NBP2-48360] - Formalin-fixed, paraffin-embedded human Ovarian Carcinoma stained with MUC-1 / CA15-3 / EMA Mouse Monoclonal Antibody (MUC1/955).](http://images.novusbio.com/fullsize/MUC1-Antibody-MUC1-955-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48360-img0001.jpg)
![Immunohistochemistry-Paraffin: MUC1 Antibody (MUC1/955) - IHC-Prediluted [NBP2-48360] - Formalin-fixed, paraffin-embedded human Breast Carcinoma stained with MUC-1 / CA15-3 / EMA Mouse Monoclonal Antibody (MUC1/955).](http://images.novusbio.com/fullsize/MUC1-Antibody-MUC1-955-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48360-img0002.jpg)
![Immunohistochemistry-Paraffin: MUC1 Antibody (SPM492) [NBP2-44667] - Human Endometrial Carcinoma stained with EMA Monoclonal Antibody (SPM492).](http://images.novusbio.com/fullsize/MUC1-Antibody-SPM492-Immunohistochemistry-Paraffin-NBP2-44667-img0001.jpg "Immunohistochemistry-Paraffin: MUC1 Antibody (SPM492) [NBP2-44667] - Human Endometrial Carcinoma stained with EMA Monoclonal Antibody (SPM492).")
![Flow Cytometry: CD45 Antibody (YW62.3) [NB100-65366] - Analysis using the FITC conjugate of CD45 antibody (YW62.3) [NB100-65366]. Staining of Mouse splenocytes.](http://images.novusbio.com/fullsize/CD45-Antibody-YW62-3-Flow-Cytometry-NB100-65366-img0006.jpg "Flow Cytometry: CD45 Antibody (YW62.3) [NB100-65366] - Analysis using the FITC conjugate of CD45 antibody (YW62.3) [NB100-65366]. Staining of Mouse splenocytes.")
![Flow Cytometry: CD45 Antibody (YW62.3) [NB100-65366] - Staining of mouse spleen cells with CD45 antibody (YW62.3) [NB100-65366].](http://images.novusbio.com/fullsize/CD45-Antibody-YW62-3-Flow-Cytometry-NB100-65366-img0003.jpg)
![Flow Cytometry: CD45 Antibody (YW62.3) [NB100-65366] - Staining of mouse spleen cells with the PE-conjugated version of CD45 antibody (YW62.3) [NB100-65366].](http://images.novusbio.com/fullsize/CD45-Antibody-YW62-3-Flow-Cytometry-NB100-65366-img0005.jpg)
![Immunocytochemistry/ Immunofluorescence: TREM2 Antibody [NBP3-35146] - Immunofluorescence analysis of PC-12 cells using TREM2 Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-35146_rabbit-trem2-pab-1012202411343353.jpg "Immunocytochemistry/ Immunofluorescence: TREM2 Antibody [NBP3-35146] - Immunofluorescence analysis of PC-12 cells using TREM2 Rabbit pAb at dilution of 1:50 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.")
![Western Blot: TREM2 Antibody [NBP3-35146] - Western Blot analysis of lysates from Rat lung using TREM2 Rabbit pAb at 1:2000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 30s.](http://images.novusbio.com/fullsize/nbp3-35146_rabbit-trem2-pab-311202517313.jpg)
![Immunohistochemistry-Paraffin: Ly-6G Antibody (RM0064-6D17) [NBP2-11784] - Staining of paraffin sections of mouse kidney and spleen tissues from LPS exposed animals.](http://images.novusbio.com/fullsize/Ly-6G-Antibody-RM0064-6D17-Immunohistochemistry-Paraffin-NBP2-11784-img0001.jpg "Immunohistochemistry-Paraffin: Ly-6G Antibody (RM0064-6D17) [NBP2-11784] - Staining of paraffin sections of mouse kidney and spleen tissues from LPS exposed animals.")
![Western Blot: LYVE-1 Antibody (JF0979) [NBP2-66940] - Western blot analysis of LYVE-1 on different lysates with Rabbit anti-LYVE1 antibody at 1/500 dilution.Lane 1: MCF-7 cell lysateLane 2: SW480 cell lysateLane 3: A431 cell lysateLane 4: HUVEC cell lysateLysates/proteins at 10 µg/Lane.Predicted band size: 35 kDaObserved band size: 35 kDaExposure time: 2 minutes;10% 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 at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp2-66940_rabbit-monoclonal-lyve-1-antibody-jf0979-western-blot-1572024145956..jpg "Western Blot: LYVE-1 Antibody (JF0979) [NBP2-66940] - Western blot analysis of LYVE-1 on different lysates with Rabbit anti-LYVE1 antibody at 1/500 dilution.Lane 1: MCF-7 cell lysateLane 2: SW480 cell lysateLane 3: A431 cell lysateLane 4: HUVEC cell lysateLysates/proteins at 10 µg/Lane.Predicted band size: 35 kDaObserved band size: 35 kDaExposure time: 2 minutes;10% 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 at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.")
![Western Blot: LYVE-1 Antibody (JF0979) [NBP2-66940] - Western blot analysis of LYVE-1 on different lysates with Rabbit anti-LYVE-1 antibody at 1/1,000 dilution.Lane 1: A549-si NT cell lysateLane 2: A549-si LYVE-1 cell lysateLysates/proteins at 10 µg/Lane.Predicted band size: 35 kDaObserved band size: 35 kDaExposure time: 3 minutes;4-20% SDS-PAGE gel.NBP2-66940 was shown to specifically react with LYVE-1 in A549-si NT cells. Weakened band was observed when A549-si LYVE-1 sample was tested. A549-si NT and Hela-si LYVE-1 samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary antibody (ET1702-29, 1/1,000) and Loading control antibody (Rabbit anti-GAPDH, 1/10,000) were used in 5% BSA 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/nbp2-66940_rabbit-monoclonal-lyve-1-antibody-jf0979-western-blot-15720241537..jpg)
![Flow Cytometry: LYVE-1 Antibody (JF0979) [NBP2-66940] - Analysis of HUVEC cells with LYVE1 antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody](http://images.novusbio.com/fullsize/LYVE-1-Antibody-JF0979-Flow-Cytometry-NBP2-66940-img0001.jpg)
![Immunohistochemistry-Paraffin: AIF-1/Iba1 Antibody (031) [NBP2-90271] - Immunochemical staining of human AIF-1/Iba1 in human spleen with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/AIF-1-Iba1-Antibody-031-Immunohistochemistry-Paraffin-NBP2-90271-img0002.jpg "Immunohistochemistry-Paraffin: AIF-1/Iba1 Antibody (031) [NBP2-90271] - Immunochemical staining of human AIF-1/Iba1 in human spleen with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).")
![Immunohistochemistry-Paraffin: AIF-1/Iba1 Antibody (031) [NBP2-90271] - Immunochemical staining of human AIF-1/Iba1 in human brain with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/AIF-1-Iba1-Antibody-031-Immunohistochemistry-Paraffin-NBP2-90271-img0001.jpg)
![Immunocytochemistry/ Immunofluorescence: AIF-1/Iba1 Antibody (031) [NBP2-90271] - Immunofluorescence staining of AIF-1/Iba1 in K562 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP2-90271 (dilution ratio 1:60) at 4 overnight. Then cells were stained with the Alexa Fluor488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Cytoplasm and Cell membrane.](http://images.novusbio.com/fullsize/nbp2-90271_rabbit-monoclonal-aif-1-iba1-antibody-031-235202514492357.png)
![Immunocytochemistry/Immunofluorescence: Ly-6G/Ly-6C Antibody (RB6-8C5) - Chimeric [NBP3-11978] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes immobilized on Shi-fix(TM) cover-slips and stained with the chimeric rabbit IgG version of RB6-8C5 (NBP3-11978) at 10 ug/ml followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining in subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-11978, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody (NBP2-52638) followed by Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/Ly-6G-Ly-6C-Antibody-RB6-8C5-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-11978-img0001.jpg "Immunocytochemistry/Immunofluorescence: Ly-6G/Ly-6C Antibody (RB6-8C5) - Chimeric [NBP3-11978] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes immobilized on Shi-fix(TM) cover-slips and stained with the chimeric rabbit IgG version of RB6-8C5 (NBP3-11978) at 10 ug/ml followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining in subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-11978, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody (NBP2-52638) followed by Alexa Fluor(R) 488 secondary antibody.")
![Flow Cytometry: Ly-6G/Ly-6C Antibody (RB6-8C5) - Chimeric [NBP3-11978] - Mouse splenocytes were stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of RB6-8C5 (NBP3-11978, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-rabbit IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Ly-6G-Ly-6C-Antibody-RB6-8C5-Chimeric-Flow-Cytometry-NBP3-11978-img0002.jpg)