| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | AF2685-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | AF3389-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | MAB2685-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | MAB3389-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | MAB3807-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-05396-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26303-50ul | |||
![Western Blot: Src Antibody (5A18) [NBP1-19188] - Human breast cancer cell line MDA-MB-231 was treated with carboplatin for 72 hours and the expression of p-Src at Y419 and total Src were detected by western blot. From a verified customer review.](http://images.novusbio.com/fullsize/Src-Antibody-5A18-Western-Blot-NBP1-19188-img0004.jpg "Western Blot: Src Antibody (5A18) [NBP1-19188] - Human breast cancer cell line MDA-MB-231 was treated with carboplatin for 72 hours and the expression of p-Src at Y419 and total Src were detected by western blot. From a verified customer review.")
![Immunohistochemistry: Src Antibody (5A18) [NBP1-19188] - IHC Analysis: Human prostate tissue stained with Src, mAb (5A18) at 20 ug/ml.](http://images.novusbio.com/fullsize/Src-Antibody-5A18-Immunohistochemistry-NBP1-19188-img0002.jpg)
![Western Blot: Src Antibody (5A18) [NBP1-19188] - Western blot analysis of Src using 20 ug of whole cell lysate (Lane 2=HeLa, Lane 3=3T3, Lane 4=PC12) probed with with Src, mAb (5A18) at 1 ug/ml.](http://images.novusbio.com/fullsize/Src-Antibody-5A18-Western-Blot-NBP1-19188-img0003.jpg)
![Immunohistochemistry: Src Antibody (5A18) [NBP1-19188] - IHC Analysis: Human adrenal tissue stained with Src, mAb (5A18) at 20 ug/ml.](http://images.novusbio.com/fullsize/Src-Antibody-5A18-Immunohistochemistry-NBP1-19188-img0001.jpg)
![ELISA Src [p Tyr419] [Biotin]](http://images.novusbio.com/fullsize2/dyc2685-2_human-phospho-src-y419-duoset-ic-elisa-2-plate-elisa-169202092434.jpg "ELISA Src [p Tyr419] [Biotin]")
![Immunoprecipitation: Src Antibody (7G6M9) [Src] - Immunoprecipitation analysis of 600 ug extracts of Mouse brain using 3 ug Src antibody . Western blot was performed from the immunoprecipitate using Src antibody at a dilution of 1:1000.](http://images.novusbio.com/fullsize/nbp3-15675_rabbit-src-mab-7g6m9-5220251733581.jpg "Immunoprecipitation: Src Antibody (7G6M9) [Src] - Immunoprecipitation analysis of 600 ug extracts of Mouse brain using 3 ug Src antibody . Western blot was performed from the immunoprecipitate using Src antibody at a dilution of 1:1000.")
![Western Blot: Src Antibody (7G6M9) [NBP3-15675] - Western blot analysis of extracts of Jurkat cells, using Src antibody (NBP3-15675) 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 Basic Kit. Exposure time: 1min.](http://images.novusbio.com/fullsize/Src-Antibody-7G6M9-Western-Blot-NBP3-15675-img0004.jpg)
![Western Blot: Src Antibody (7G6M9) [NBP3-15675] - Western blot analysis of extracts of various cell lines, using Src antibody (NBP3-15675) 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 Basic Kit. Exposure time: 1s.](http://images.novusbio.com/fullsize/Src-Antibody-7G6M9-Western-Blot-NBP3-15675-img0003.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: Src Antibody (7G6M9) [NBP3-15675] - Western blot analysis of extracts from normal (control) and Src knockout (KO) HeLa cells, using Src antibody (NBP3-15675) 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 Basic Kit. Exposure time: 1min.](http://images.novusbio.com/fullsize/Src-Antibody-7G6M9-Knockout-Validated-NBP3-15675-img0001.jpg)
![Immunocytochemistry/ Immunofluorescence: Src Antibody (7G6M9) [Src] - Confocal imaging of NIH/3T3 cells using [KO Validated] Src Rabbit mAb . The cells were counterstained with alpha-Tubulin Mouse mAb (Green). DAPI was used for nuclear staining (blue). Objective: 100x.](http://images.novusbio.com/fullsize/nbp3-15675_rabbit-src-mab-7g6m9-5220251733591.jpg)
![Immunocytochemistry/ Immunofluorescence: Src Antibody (7G6M9) [Src] - Confocal imaging of A549 cells using [KO Validated] Src Rabbit mAb . The cells were counterstained with alpha-Tubulin Mouse mAb (Green). DAPI was used for nuclear staining (blue). Objective: 100x.](http://images.novusbio.com/fullsize/nbp3-15675_rabbit-src-mab-7g6m9-52202517363716.jpg)
![Western Blot: Src [p Tyr529] Antibody [NBP3-05396] - Western blot analysis of extracts of various cell lines, using Src pAb (NBP3-05396) at 1:1000 dilution.Hela cells were treated by ATP(5 mM) at 30C for 1 hour or treated by CIP(20uL/400ul) at 37C for 1 hour. 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: 180s.](http://images.novusbio.com/fullsize/Src [p Tyr529] Antibody-Western Blot-NBP3-05396-img0001.jpg "Western Blot: Src [p Tyr529] Antibody [NBP3-05396] - Western blot analysis of extracts of various cell lines, using Src pAb (NBP3-05396) at 1:1000 dilution.Hela cells were treated by ATP(5 mM) at 30C for 1 hour or treated by CIP(20uL/400ul) at 37C for 1 hour. 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: 180s.")
![Western Blot: Src [p Tyr529] Antibody - Azide and BSA Free [Src] - Western blot analysis of lysates from A-431 cells, using Src Rabbit pAb at 1:1000 dilution. A-431 cells were treated by EGF (100 ng/ml) at 37C for 30 minutes after serum-starvation overnight.Secondary antibody: HRP-conjugated 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 Basic Kit .Exposure time: 60s.](http://images.novusbio.com/fullsize/nbp3-05396_rabbit-polyclonal-src-p-tyr529-antibody-52202516293989.jpg)
![Western Blot: Src Antibody (21H5) [NBP3-26303] - Positive Western Blot detected in: NIH/3T3 whole cell lysate, MCF-7 whole cell lysate. All lanes: Src Antibody at 1.2ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 60, 61 KDa Observed band size: 60, 61 KDa](http://images.novusbio.com/fullsize/nbp3-26303_rabbit-src-mab-21h5-282202411472113.jpg "Western Blot: Src Antibody (21H5) [NBP3-26303] - Positive Western Blot detected in: NIH/3T3 whole cell lysate, MCF-7 whole cell lysate. All lanes: Src Antibody at 1.2ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 60, 61 KDa Observed band size: 60, 61 KDa")
![Immunocytochemistry/Immunofluorescence: Src Antibody (21H5) [NBP3-26303] - Staining of MCF-7 cells with Src Antibody (21H5) at 1:39, 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/nbp3-26303_rabbit-src-mab-21h5-28220241312247.jpg)
![Flow Cytometry: Src Antibody (21H5) [NBP3-26303] - Overlay histogram showing SH-SY5Y cells stained with Src Antibody (21H5) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4C. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26303_rabbit-src-mab-21h5-282202414183653.jpg)
![Western Blot: Src [p Tyr527] Antibody [NBP3-13245] - Untreated (-) and treated (+) NIH-3T3 whole cell extracts (20 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Src (phospho Tyr527) antibody (NBP3-13245) 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/Src-[p-Tyr527]-Antibody-Western-Blot-NBP3-13245-img0004.jpg "<b>Biological Strategies Validation. </b>Western Blot: Src [p Tyr527] Antibody [NBP3-13245] - Untreated (-) and treated (+) NIH-3T3 whole cell extracts (20 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Src (phospho Tyr527) antibody (NBP3-13245) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![<b>Biological Strategies Validation. </b>Western Blot: Src [p Tyr527] Antibody [NBP3-13245] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Src (phospho Tyr529) antibody (NBP3-13245) 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/Src-[p-Tyr527]-Antibody-Western-Blot-NBP3-13245-img0001.jpg)
![Western Blot: Src [p Tyr527] Antibody [NBP3-13245] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Src (phospho Tyr527) antibody (NBP3-13245) 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/Src-[p-Tyr527]-Antibody-Western-Blot-NBP3-13245-img0003.jpg)