| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-61909-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-61908-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-61909-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-61908-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52716-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | MAB7489-SP | |||
![Flow Cytometry: CD1.1 antigen Antibody (CB3) [NBP1-28362] - Chicken peripheral blood mononuclear cells were stained with Mouse Anti-Chicken CD1.1-FITC and Mouse Anti-Chicken CD3-PE.](http://images.novusbio.com/fullsize/CD1-1-antigen-Antibody-CB3-Flow-Cytometry-NBP1-28362-img0001.jpg "Flow Cytometry: CD1.1 antigen Antibody (CB3) [NBP1-28362] - Chicken peripheral blood mononuclear cells were stained with Mouse Anti-Chicken CD1.1-FITC and Mouse Anti-Chicken CD3-PE.")
![CD1.1 antigen Antibody (CB3) [NBP1-28362] - Chicken peripheral blood lymphocytes were stained with Mouse Anti-Chicken CD1.1-UNLB (SB Cat. No. 8430-01) followed by Goat Anti-Mouse IgG1, Human ads-PE (SB Cat. No. 1070-09).](http://images.novusbio.com/fullsize/CD1-1-antigen-Antibody-CB3-NBP1-28362-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CD19 Antibody (CVID3/429) [NBP2-44675] - Immunofluorescent staining of Raji cells. CD19 Antibody (CVID3/429) followed by goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Red Dot (Red)](http://images.novusbio.com/fullsize/CD19-Antibody-CVID3-429-Immunocytochemistry-Immunofluorescence-NBP2-44675-img0003.jpg "Immunocytochemistry/Immunofluorescence: CD19 Antibody (CVID3/429) [NBP2-44675] - Immunofluorescent staining of Raji cells. CD19 Antibody (CVID3/429) followed by goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Red Dot (Red)")
![Flow Cytometry: CD19 Antibody (CVID3/429) [NBP2-44675] - Flow cytometry analysis of lymphocyte-gated PBMCs unstained (gray) or stained with CF405S-labeled CD19 antibody (CVID3/429) (violet).](http://images.novusbio.com/fullsize/CD19-Antibody-CVID3-429-Flow-Cytometry-NBP2-44675-img0004.jpg)
![Flow Cytometry: CD19 Antibody (CVID3/429) [NBP2-44675] - Flow Cytometric Analysis of Raji cells. CD19 Antibody (CVID3/429) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/CD19-Antibody-CVID3-429-Flow-Cytometry-NBP2-44675-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CD19 Antibody (CVID3/155) [NBP2-44674] - Immunofluorescence staining of Raji cells. CD19 Antibody (CVID3/155) followed by goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Red Dot (Red).](http://images.novusbio.com/fullsize/CD19-Antibody-CVID3-155-Immunocytochemistry-Immunofluorescence-NBP2-44674-img0003.jpg "Immunocytochemistry/Immunofluorescence: CD19 Antibody (CVID3/155) [NBP2-44674] - Immunofluorescence staining of Raji cells. CD19 Antibody (CVID3/155) followed by goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Red Dot (Red).")
![Flow Cytometry: CD19 Antibody (CVID3/155) [NBP2-44674] - Flow cytometric analysis of lymphocyte-gated PBMCs. CD19 antibody (CVID3/155) labeled with CF568 (orange); unstained cells (gray).](http://images.novusbio.com/fullsize/CD19-Antibody-CVID3-155-Flow-Cytometry-NBP2-44674-img0004.jpg)
![Flow Cytometry: CD19 Antibody (CVID3/155) [NBP2-44674] - Flow Cytometric Analysis of Raji cells. CD19 Antibody (CVID3/155) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/CD19-Antibody-CVID3-155-Flow-Cytometry-NBP2-44674-img0002.jpg)
![CD19 Antibody (CVID3/429) [mFluor Violet 450 SE] [NBP2-61909MFV450] - Vial of mFluor Violet 450 conjugated antibody. mFluor Violet 450 is optimally excited at 406 nm by the Violet laser (405 nm) and has an emission maximum of 445 nm.](http://images.novusbio.com/fullsize/nbp2-61909mfv450_mouse-cd19-mab-cvid3-429-mfluor-violet-450-se-22620231235914.png "CD19 Antibody (CVID3/429) [mFluor Violet 450 SE] [NBP2-61909MFV450] - Vial of mFluor Violet 450 conjugated antibody. mFluor Violet 450 is optimally excited at 406 nm by the Violet laser (405 nm) and has an emission maximum of 445 nm.")
![Western Blot: CD19 Antibody [NBP2-15782] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CD19 antibody [C1C3] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/CD19-Antibody-Western-Blot-NBP2-15782-img0016.jpg "Western Blot: CD19 Antibody [NBP2-15782] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with CD19 antibody [C1C3] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: CD19 Antibody [NBP2-15782] - Human tonsil. CD19 stained by CD19 antibody [C1C3] diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/CD19-Antibody-Immunohistochemistry-Paraffin-NBP2-15782-img0011.jpg)
![Flow Cytometry: CD19 Antibody [NBP2-15782] - Mouse splenocytes cell fixed in 4% paraformaldehyde at 4-C for 15 min. Black: Unlabelled sample was used as a control. Red: CD19 antibody [C1C3] dilution: 1:50. Acquisition of 20,000 events were collected using a Dylight 488-conjugated secondary antibody for FACS analysis.](http://images.novusbio.com/fullsize/CD19-Antibody-Flow-Cytometry-NBP2-15782-img0006.jpg)
![Western Blot: CD19 Antibody [NBP2-15782] - Mouse tissue extract (50 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with CD19 antibody [C1C3] diluted at 1:1000.](http://images.novusbio.com/fullsize/CD19-Antibody-Western-Blot-NBP2-15782-img0007.jpg)
![Immunohistochemistry-Paraffin: CD19 Antibody [NBP2-15782] - Human tonsil. Green: CD19 stained by CD19 antibody [C1C3] diluted at 1:250.Blue: Fluoroshield with DAPI. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/CD19-Antibody-Immunohistochemistry-Paraffin-NBP2-15782-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: CD19 Antibody [NBP2-15782] -Raji cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: CD19 stained by CD19 antibody [C1C3] diluted at 1:500.Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/antibody/nbp2-15782_rabbit-polyclonal-cd19-antibody-immunocytochemistry-immunofluorescence-35202413518..jpg)
![Immunocytochemistry/Immunofluorescence: CD19 Antibody (JF100-06) [NBP2-67229] - Staining CD19 in PC-3M cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CD19-Antibody-JF100-06-Immunocytochemistry-Immunofluorescence-NBP2-67229-img0005.jpg "Immunocytochemistry/Immunofluorescence: CD19 Antibody (JF100-06) [NBP2-67229] - Staining CD19 in PC-3M cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.")
![Immunohistochemistry-Paraffin: CD19 Antibody (JF100-06) [NBP2-67229] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-CD19 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CD19-Antibody-JF100-06-Immunohistochemistry-Paraffin-NBP2-67229-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: CD19 Antibody (JF100-06) [NBP2-67229] - Staining CD19 in 293T cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CD19-Antibody-JF100-06-Immunocytochemistry-Immunofluorescence-NBP2-67229-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: CD19 Antibody (JF100-06) [NBP2-67229] - Staining CD19 in Hela cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/CD19-Antibody-JF100-06-Immunocytochemistry-Immunofluorescence-NBP2-67229-img0002.jpg)
![Immunohistochemistry-Paraffin: CD19 Antibody (JF100-06) [NBP2-67229] - Analysis of paraffin-embedded human spleen tissue using anti-CD19 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/CD19-Antibody-JF100-06-Immunohistochemistry-Paraffin-NBP2-67229-img0003.jpg)
![Western Blot: CD19 Antibody (JF100-06) [NBP2-67229] -Analysis of CD19 on different lysates with Rabbit anti-CD19 antibody at 1/1,000 dilution.Lane 1: Raji cell lysateLane 2: Daudi cell lysateLysates/proteins at 10 ug/Lane.Predicted band size: 61 kDaObserved band size: 90 kDaExposure 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 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 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp2-67229_rabbit-monoclonal-cd19-antibody-jf100-06-western-blot-1382024114350..jpg)
![Flow Cytometry: CD19 Antibody (JF100-06) [NBP2-67229] -Analysis of Daudi cells labeling CD19.Cells were fixed and permeabilized. Then stained with the primary antibody (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/nbp2-67229_rabbit-monoclonal-cd19-antibody-jf100-06-flow-cytometry-138202411462..jpg)
![Flow Cytometry: CD19 Antibody (JF100-06) [NBP2-67229] -Analysis of Raji cells labeling CD19.Cells were fixed and permeabilized. Then stained with the primary antibody (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/nbp2-67229_rabbit-monoclonal-cd19-antibody-jf100-06-flow-cytometry-1382024114721..jpg)
