| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-37734-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05380-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26406-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-44854 | |||
| Azide and BSA Free | NBP2-34804-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-49603-25ul | |||
![Western Blot: MAP2 Antibody (5B7) [NBP2-37734] - Western blot analysis using MAP2 mAb against human MAP2 recombinant protein. (Observed MW is 36.1 kDa)](http://images.novusbio.com/fullsize/MAP2-Antibody-5B7-Western-Blot-NBP2-37734-img0002.jpg "Western Blot: MAP2 Antibody (5B7) [NBP2-37734] - Western blot analysis using MAP2 mAb against human MAP2 recombinant protein. (Observed MW is 36.1 kDa)")
![Flow Cytometry: MAP2 Antibody (5B7) [NBP2-37734] - Flow cytometric analysis of HeLa cells using MAP2 Antibody (5B7) (green) and negative control (red).](http://images.novusbio.com/fullsize/MAP2-Antibody-5B7-Flow-Cytometry-NBP2-37734-img0003.jpg)
![ELISA: MAP2 Antibody (5B7) [NBP2-37734] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/MAP2-Antibody-5B7-ELISA-NBP2-37734-img0001.jpg)
![Western Blot: Elk-1 [p Ser383] Antibody [NBP3-05380] - Western blot analysis of extracts of Jurkat cells, using Elk-1 antibody (NBP3-05380) at 1:1000 dilution. Jurkat cells were treated by Anisomycin (5ug/mL) for 30 minutes after serum-starvation overnight. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 10s.](http://images.novusbio.com/fullsize/Elk-1-[p-Ser383]-Antibody-Western-Blot-NBP3-05380-img0002.jpg "Western Blot: Elk-1 [p Ser383] Antibody [NBP3-05380] - Western blot analysis of extracts of Jurkat cells, using Elk-1 antibody (NBP3-05380) at 1:1000 dilution. Jurkat cells were treated by Anisomycin (5ug/mL) for 30 minutes after serum-starvation overnight. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 10s.")
![Immunohistochemistry: Elk-1 [p Ser383] Antibody - BSA Free [Elk-1] - Immunohistochemistry analysis of paraffin-embedded Human tonsil tissue using Elk-1 Rabbit pAb at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-05380_rabbit-polyclonal-elk-1-p-ser383-antibody-52202516283228.jpg)
![Immunohistochemistry: Elk-1 [p Ser383] Antibody - BSA Free [Elk-1] - Immunohistochemistry analysis of paraffin-embedded Rat intestine tissue using Elk-1 Rabbit pAb at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-05380_rabbit-polyclonal-elk-1-p-ser383-antibody-5220251640288.jpg)
![Immunohistochemistry: Elk-1 [p Ser383] Antibody - BSA Free [Elk-1] - Immunohistochemistry analysis of paraffin-embedded Mouse cerebellum tissue using Elk-1 Rabbit pAb at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-05380_rabbit-polyclonal-elk-1-p-ser383-antibody-52202516345237.jpg)
![Immunohistochemistry: Elk-1 [p Ser383] Antibody - BSA Free [Elk-1] - Immunohistochemistry analysis of paraffin-embedded Human colon tissue using Elk-1 Rabbit pAb at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer(pH 6.0) prior to IHC staining.](http://images.novusbio.com/fullsize/nbp3-05380_rabbit-polyclonal-elk-1-p-ser383-antibody-5220251636368.jpg)
![Western Blot: JNK1/2/3 Antibody (0J5D8) [NBP3-16250] - Western blot analysis of extracts of various cell lines, using JNK1/2/3 Rabbit mAb (NBP3-16250) 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: 30s.](http://images.novusbio.com/fullsize/JNK1-2-3-Antibody-0J5D8-Western-Blot-NBP3-16250-img0002.jpg "Western Blot: JNK1/2/3 Antibody (0J5D8) [NBP3-16250] - Western blot analysis of extracts of various cell lines, using JNK1/2/3 Rabbit mAb (NBP3-16250) 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: 30s.")
![Immunohistochemistry: JNK1/2/3 Antibody (0J5D8) [NBP3-16250] - Immunofluorescence analysis of mouse brain using JNK1/2/3 Rabbit mAb (NBP3-16250) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/JNK1-2-3-Antibody-0J5D8-Immunohistochemistry-NBP3-16250-img0001.jpg)
![Immunohistochemistry: TOR/mTOR [p Ser2448] Antibody (1G6) [NBP3-26406] - Image of TOR/mTOR [p Ser2448] Antibody (1G6) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26406_rabbit-tor-mtor-p-ser-2448-mab-1g6-2622024152248.jpg "Immunohistochemistry: TOR/mTOR [p Ser2448] Antibody (1G6) [NBP3-26406] - Image of TOR/mTOR [p Ser2448] Antibody (1G6) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Western Blot: TOR/mTOR [p Ser2448] Antibody (1G6) [NBP3-26406] - Positive Western Blot detected in Hela whole cell lysate, A549 whole cell lysate. All lanes: TOR/mTOR [p Ser2448] Antibody at 0.825ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 289 KDa Observed band size: 289 KDa](http://images.novusbio.com/fullsize/nbp3-26406_rabbit-tor-mtor-p-ser-2448-mab-1g6-28220241140938.jpg)
![Immunocytochemistry/Immunofluorescence: TOR/mTOR [p Ser2448] Antibody (1G6) [NBP3-26406] - Staining of Hela cells with TOR/mTOR [p Ser2448] Antibody (1G6) at 1:100, 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/nbp3-26406_rabbit-tor-mtor-p-ser-2448-mab-1g6-28220241312233.jpg)
![Immunohistochemistry-Paraffin: CD45 Antibody (SPM570) [NBP2-32935] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD45 antibody (SPM570) [NBP2-32935].](http://images.novusbio.com/fullsize/CD45-Antibody-SPM570-Immunohistochemistry-Paraffin-NBP2-32935-img0003.jpg "Immunohistochemistry-Paraffin: CD45 Antibody (SPM570) [NBP2-32935] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD45 antibody (SPM570) [NBP2-32935].")
![Immunohistochemistry-Paraffin: CD45 Antibody (SPM570) [NBP2-32935] - Formalin-fixed, paraffin-embedded human tonsil (10X) stained with CD45 antibody (SPM570).](http://images.novusbio.com/fullsize/nbp2-32935_mouse-monoclonal-cd45-antibody-spm570-17720241044627.jpg)
![Western Blot: MAP1 Antibody (4A1) [H00064112-M02] - Analysis of MOAP1 expression in transfected 293T cell line by MOAP1 monoclonal antibody (M02), clone 4A1.Lane 1: MOAP1 transfected lysate(39.5 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/MAP1-Antibody-4A1-Western-Blot-H00064112-M02-img0004.jpg "Western Blot: MAP1 Antibody (4A1) [H00064112-M02] - Analysis of MOAP1 expression in transfected 293T cell line by MOAP1 monoclonal antibody (M02), clone 4A1.Lane 1: MOAP1 transfected lysate(39.5 KDa).Lane 2: Non-transfected lysate.")
![Immunocytochemistry/Immunofluorescence: MAP1 Antibody (4A1) [H00064112-M02] - Analysis of monoclonal antibody to MOAP1 on HeLa cell . Antibody concentration 10 ug/ml.](http://images.novusbio.com/fullsize/MAP1-Antibody-4A1-Immunocytochemistry-Immunofluorescence-H00064112-M02-img0002.jpg)
![Sandwich ELISA: MAP1 Antibody (4A1) [H00064112-M02] - Detection limit for recombinant GST tagged MOAP1 is 0.3 ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/MAP1-Antibody-4A1-Sandwich-ELISA-H00064112-M02-img0003.jpg)
![Western Blot: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Western blot analysis of p16INK4a/CDKN2A on different lysates with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: HepG2 cell lysate Lane 3: HEK-293 cell lysate Lane 4: NIH:OVCAR-3 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 16 kDa Observed band size: 16 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 (NBP3-32688) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32688_mouse-p16ink4a-cdkn2a-mab-pd01-16-2882024142262.jpg "Western Blot: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Western blot analysis of p16INK4a/CDKN2A on different lysates with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: HepG2 cell lysate Lane 3: HEK-293 cell lysate Lane 4: NIH:OVCAR-3 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 16 kDa Observed band size: 16 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 (NBP3-32688) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/500 dilution. 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 (NBP3-32688) 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/nbp3-32688_mouse-p16ink4a-cdkn2a-mab-pd01-16-29820241426269.jpg)
![Immunocytochemistry/ Immunofluorescence: p16INK4a/CDKN2A Antibody (PD01-16) [NBP3-32688] - Immunocytochemistry analysis of HeLa cells labeling p16INK4a/CDKN2A with Mouse anti-p16INK4a/CDKN2AINK4a/CDKN2A antibody (NBP3-32688) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-p16INK4a/CDKN2A antibody (NBP3-32688) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32688_mouse-p16ink4a-cdkn2a-mab-pd01-16-29202410334055.jpg)
![Western Blot: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32811) at 1/1,000 dilution. Lane 1: Human brain tissue lysate Lane 2: Rat brain tissue lysate Lysates/proteins at 50 ug/Lane. Predicted band size: 46 kDa Observed band size: 35-100 kDa Exposure time: 5 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 (NBP3-32811) 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/nbp3-32811_rabbit-tau-p-thr231-mab-psh01-04-288202412461627.jpg "Western Blot: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32811) at 1/1,000 dilution. Lane 1: Human brain tissue lysate Lane 2: Rat brain tissue lysate Lysates/proteins at 50 ug/Lane. Predicted band size: 46 kDa Observed band size: 35-100 kDa Exposure time: 5 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 (NBP3-32811) 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: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Immunofluorescence analysis of paraffin-embedded mouse hippocampus tissue labeling Tau with Rabbit anti-Tau antibody (NBP3-32811) 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32811, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32811_rabbit-tau-p-thr231-mab-psh01-04-29820241492636.jpg)
![Immunohistochemistry: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-Tau antibody (NBP3-32811) at 1/1,000 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 (NBP3-32811) at 1/1,000 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/nbp3-32811_rabbit-tau-p-thr231-mab-psh01-04-29820241420935.jpg)
![Immunoprecipitation: Astrin Antibody - BSA Free [NBP3-45856] - IP Result of anti-Astrin (IP:, 5ug; Detection: 1:1000) with HeLa cells lysate 3000ug.](http://images.novusbio.com/fullsize/nbp3-45856_rabbit-astrin-pab-bsa-free-284202512365487.jpg "Immunoprecipitation: Astrin Antibody - BSA Free [NBP3-45856] - IP Result of anti-Astrin (IP:, 5ug; Detection: 1:1000) with HeLa cells lysate 3000ug.")
![Immunohistochemistry: Astrin Antibody - BSA Free [NBP3-45856] - Immunohistochemistry of paraffin-embedded human testis using (Astrin antibody) at dilution of 1:100](http://images.novusbio.com/fullsize/nbp3-45856_rabbit-astrin-pab-bsa-free-28420251304157.jpg)
![Western Blot: Astrin Antibody - BSA Free [NBP3-45856] - HeLa cells were subjected to SDS PAGE followed by western blot with (Astrin antibody) at dilution of 1:1000](http://images.novusbio.com/fullsize/nbp3-45856_rabbit-astrin-pab-bsa-free-284202512365472.jpg)
![Immunohistochemistry-Paraffin: Tau Antibody [NBP2-49603] - Staining of human skeletal muscle shows moderate cytoplasmic positivity in myocytes.](http://images.novusbio.com/fullsize/antibody/nbp2-49603_rabbit-polyclonal-tau-antibody-immunohistochemistry-paraffin-31202591128..png "Immunohistochemistry-Paraffin: Tau Antibody [NBP2-49603] - Staining of human skeletal muscle shows moderate cytoplasmic positivity in myocytes.")
![Immunohistochemistry-Paraffin: Tau Antibody [NBP2-49603] - Staining of human kidney shows strong cytoplasmic positivity in cells in glomeruli and moderate cytoplasmic positivity in cells in tubules.](http://images.novusbio.com/fullsize/antibody/nbp2-49603_rabbit-polyclonal-tau-antibody-immunohistochemistry-paraffin-31202591256..png)
![Immunohistochemistry-Paraffin: Tau Antibody [NBP2-49603] -Staining of human fallopian tube shows negative positivity in glandular cells as expected.](http://images.novusbio.com/fullsize/antibody/nbp2-49603_rabbit-polyclonal-tau-antibody-immunohistochemistry-paraffin-31202591414..png)
![Immunohistochemistry-Paraffin: Tau Antibody [NBP2-49603] - Staining of human liver shows no positivity in hepatocytes as expected.](http://images.novusbio.com/fullsize/antibody/nbp2-49603_rabbit-polyclonal-tau-antibody-immunohistochemistry-paraffin-31202591526..png)
![Western Blot: p38 alpha [p Tyr323] Antibody [NBP3-23249] - A) Western blot image of GST-recombinant p38 (K53M) mutant kinase untreated (lanes 1 & 3) or treated with Fyn kinase (lanes 2 & 4). B) Western blot analysis of p38 phosphorylation in mouse macrophages stimulated with 1 mM pervanadate for 30 min. (lanes 1 & 3) then the blot was treated with alkaline phosphatase (lanes 2 & 4). Both blots were probed with anti-p38 alpha (a.a. 319-328) (lanes 1 & 2) or anti-p38 alpha (Tyr-323) (lanes 3 & 4).](http://images.novusbio.com/fullsize/nbp3-23249_rabbit-p38-alpha-p-tyr323-pab-19920231410135.jpg "Western Blot: p38 alpha [p Tyr323] Antibody [NBP3-23249] - A) Western blot image of GST-recombinant p38 (K53M) mutant kinase untreated (lanes 1 & 3) or treated with Fyn kinase (lanes 2 & 4). B) Western blot analysis of p38 phosphorylation in mouse macrophages stimulated with 1 mM pervanadate for 30 min. (lanes 1 & 3) then the blot was treated with alkaline phosphatase (lanes 2 & 4). Both blots were probed with anti-p38 alpha (a.a. 319-328) (lanes 1 & 2) or anti-p38 alpha (Tyr-323) (lanes 3 & 4).")
![Immunocytochemistry/Immunofluorescence: p38 alpha [p Tyr323] Antibody [NBP3-23249] - Immunocytochemical labeling of p38 MAPK in pervanadate-treated mouse C2C12. The cells were labeled with mouse monoclonal p38 alpha MAPK and rabbit polyclonal p38 MAPK (Tyr-323) antibodies, then the antibodies were detected using appropriate secondary antibodies conjugated to Cy3.](http://images.novusbio.com/fullsize/nbp3-23249_rabbit-p38-alpha-p-tyr323-pab-19920231911472.jpg)
![Immunohistochemistry-Paraffin: MAP2 Antibody (HL1656) - Azide and BSA Free [NBP3-25555] - MAP2 antibody [HL1656] detects MAP2 protein at cell membrane and cytoplasm by immunohistochemical analysis. Sample: Paraffin-embedded rat brain. MAP2 stained by MAP2 antibody [HL1656] (NBP3-25555) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25555_rabbit-map2-mab-hl1656-azide-and-bsa-free-212024939165.jpg "Immunohistochemistry-Paraffin: MAP2 Antibody (HL1656) - Azide and BSA Free [NBP3-25555] - MAP2 antibody [HL1656] detects MAP2 protein at cell membrane and cytoplasm by immunohistochemical analysis. Sample: Paraffin-embedded rat brain. MAP2 stained by MAP2 antibody [HL1656] (NBP3-25555) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min")
![Immunocytochemistry/Immunofluorescence: MAP2 Antibody (HL1656) - Azide and BSA Free [NBP3-25555] - MAP2 antibody [HL1656] detects MAP2 protein in dendrites, but not in axons, by immunofluorescent analysis. Sample: DIV9 rat E18 primary hippocampal neuron cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: MAP2 stained by MAP2 antibody [HL1656] (NBP3-25555) diluted at 1:250. Red: Tau, an axon marker, stained by Tau antibody [GT287] diluted at 1:500. Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-25555_rabbit-map2-mab-hl1656-azide-and-bsa-free-212024941460.jpg)
![Immunohistochemistry-Paraffin: MAP2 Antibody (HL1656) - Azide and BSA Free [NBP3-25555] - MAP2 antibody [HL1656] detects MAP2 protein at cell membrane and cytoplasm by immunohistochemical analysis. Sample: Paraffin-embedded mouse brain. MAP2 stained by MAP2 antibody [HL1656] (NBP3-25555) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25555_rabbit-map2-mab-hl1656-azide-and-bsa-free-2120249413331.jpg)