| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | AF2538-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | MAB25382-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | MAB2538-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | DYC6170E | |||
| Carrier Free | DYC6170-5 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier Free | DYC2538-5 | |||
![Western Blot: DDR2 Antibody [NBP2-14926] - Wild-type (WT) and DDR2 (KO) HeLa cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DDR2 antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/DDR2-Antibody-Western-Blot-NBP2-14926-img0006.jpg "Western Blot: DDR2 Antibody [NBP2-14926] - Wild-type (WT) and DDR2 (KO) HeLa cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DDR2 antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: DDR2 Antibody [NBP2-14926] - DIV9 rat E18 primary cortical neuron and glia cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: DDR2 stained by DDR2 antibody [C2C3], C-term diluted at 1:250.Red: Tau, an Axon marker, stained by Tau antibody [287] diluted at 1:500.Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/DDR2-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-14926-img0007.jpg)
![Immunohistochemistry-Paraffin: DDR2 Antibody [NBP2-14926] - Human breast cancer, using DDR2 antibody at 1:250 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min](http://images.novusbio.com/fullsize/DDR2-Antibody-Immunohistochemistry-Paraffin-NBP2-14926-img0001.jpg)
![Western Blot: DDR2 Antibody [NBP2-14926] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DDR2 antibody diluted at 1:3000.](http://images.novusbio.com/fullsize/DDR2-Antibody-Western-Blot-NBP2-14926-img0004.jpg)
![Western Blot: DDR2 Antibody [NBP2-14926] - U87-MG whole cell and membrane extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DDR2 antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/DDR2-Antibody-Western-Blot-NBP2-14926-img0005.jpg)
![Western Blot: DDR2 Antibody [NBP2-14926] - Mouse tissue extract (50 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with DDR2 antibody [C2C3], C-term (NBP2-14926) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-14926_rabbit-polyclonal-ddr2-antibody-91020242063328.jpg)
![Western Blot: DDR2 Antibody (HL1107) [NBP3-13724] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with DDR2 antibody [HL1107] (NBP3-13724) 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/DDR2-Antibody-HL1107-Western-Blot-NBP3-13724-img0005.jpg "<b>Genetic Strategies Validation. </b>Western Blot: DDR2 Antibody (HL1107) [NBP3-13724] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with DDR2 antibody [HL1107] (NBP3-13724) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Western Blot: DDR2 Antibody (HL1107) [NBP3-13724] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with DDR2 antibody [HL1107] (NBP3-13724) 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/DDR2-Antibody-HL1107-Western-Blot-NBP3-13724-img0002.jpg)
![Western Blot: DDR2 Antibody (HL1107) [NBP3-13724] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with DDR2 antibody [HL1107] (NBP3-13724) diluted at 1:500000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-13724_rabbit-ddr2-mab-hl1107-91020242011494.jpg)
![Immunohistochemistry-Paraffin: DDR2 Antibody (HL1107) [NBP3-13724] - DDR2 antibody [HL1107] detects DDR2 protein by immunohistochemical analysis.Sample: Paraffin-embedded rat tissues.DDR2 stained by DDR2 antibody [HL1107] (NBP3-13724) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13724_rabbit-ddr2-mab-hl1107-91020242001079.jpg)
![<b>Orthogonal Strategies Validation. </b> Paraffin-embedded mouse tissues.DDR2 stained by DDR2 antibody [HL1107] diluted at 1:16000.Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13724_rabbit-ddr2-mab-hl1107-immunohistochemistry-paraffin-317202591257..png)
![Mouse testis. DDR2 stained by DDR2 antibody [HL1107] diluted at 1:16000.Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13724_rabbit-ddr2-mab-hl1107-immunohistochemistry-paraffin-317202591418..png)
![<b>Orthogonal Strategies Validation. </b> Mouse tissues.DDR2 stained by DDR2 antibody [HL1107] diluted at 1:16000.Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13724_rabbit-ddr2-mab-hl1107-immunohistochemistry-paraffin-317202591535..png)
![Western Blot: DDR2 Antibody (3B11E4) [NBP1-28883] - Analysis using DDR2 mouse mAb against truncated DDR2 recombinant protein.](http://images.novusbio.com/fullsize/DDR2-Antibody-3B11E4-Western-Blot-NBP1-28883-img0009.jpg "Western Blot: DDR2 Antibody (3B11E4) [NBP1-28883] - Analysis using DDR2 mouse mAb against truncated DDR2 recombinant protein.")
![Immunocytochemistry/Immunofluorescence: DDR2 Antibody (3B11E4) [NBP1-28883] - Analysis of A549 cells using DDR2 mouse mAb (green). Red: Actin filaments have been labeled with DY-554 phalloidin. Blue: DRAQ5 fluorescent DNA dye.](http://images.novusbio.com/fullsize/DDR2-Antibody-3B11E4-Immunocytochemistry-Immunofluorescence-NBP1-28883-img0006.jpg)
![Immunohistochemistry-Paraffin: DDR2 Antibody (3B11E4) [NBP1-28883] - Analysis of human skeletal musle tissues using DDR2 mouse mAb.](http://images.novusbio.com/fullsize/DDR2-Antibody-3B11E4-Immunohistochemistry-Paraffin-NBP1-28883-img0008.jpg)
![ELISA DDR2 [Biotin]](http://images.novusbio.com/fullsize2/dyc2538-2_human-total-ddr2-duoset-ic-elisa-2-plate-elisa-16920209313.jpg "ELISA DDR2 [Biotin]")
![Western Blot: DDR2 Antibody (JE31-45) [NBP3-32260] - Western blot analysis of DDR2 on different lysates with Rabbit anti-DDR2 antibody (NBP3-32260) at 1/1,000 dilution. Lane 1: HeLa cell lysate (40 ug/Lane) Lane 2: SH-SY5Y cell lysate (40 ug/Lane) Lane 3: L929 cell lysate (40 ug/Lane) Lane 4: NIH/3T3 cell lysate (40 ug/Lane) Lane 5: U-2 OS cell lysate (15 ug/Lane) Lane 6: A375 cell lysate (15 ug/Lane) Lane 7: PC-12 cell lysate (10 ug/Lane) Predicted band size: 97 kDa Observed band size: 97 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 (NBP3-32260) 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/nbp3-32260_rabbit-ddr2-mab-je31-45-27820241631680.jpg "Western Blot: DDR2 Antibody (JE31-45) [NBP3-32260] - Western blot analysis of DDR2 on different lysates with Rabbit anti-DDR2 antibody (NBP3-32260) at 1/1,000 dilution. Lane 1: HeLa cell lysate (40 ug/Lane) Lane 2: SH-SY5Y cell lysate (40 ug/Lane) Lane 3: L929 cell lysate (40 ug/Lane) Lane 4: NIH/3T3 cell lysate (40 ug/Lane) Lane 5: U-2 OS cell lysate (15 ug/Lane) Lane 6: A375 cell lysate (15 ug/Lane) Lane 7: PC-12 cell lysate (10 ug/Lane) Predicted band size: 97 kDa Observed band size: 97 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 (NBP3-32260) 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: DDR2 Antibody (JE31-45) [NBP3-32260] - Immunohistochemical analysis of paraffin-embedded rat skeletal muscle tissue with Rabbit anti-DDR2 antibody (NBP3-32260) at 1/200 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 (NBP3-32260) at 1/200 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/nbp3-32260_rabbit-ddr2-mab-je31-45-298202414161855.jpg)
![Western Blot: DDR2 Antibody (1M8U7) [NBP3-16371] - Western blot analysis of extracts of various cell lines, using DDR2 Rabbit mAb (NBP3-16371) 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: 10s.](http://images.novusbio.com/fullsize/DDR2-Antibody-1M8U7-Western-Blot-NBP3-16371-img0001.jpg "Western Blot: DDR2 Antibody (1M8U7) [NBP3-16371] - Western blot analysis of extracts of various cell lines, using DDR2 Rabbit mAb (NBP3-16371) 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: 10s.")