Note: Mouseover a species abbreviation on the product page to display the fullname.
How can we help you?
![Western Blot: Synapsin I [p Ser549] Antibody [NB300-744] - Western blot of rat brain lysate showing specific immunolabeling of the ~78k synapsin I phosphorylated at Ser549 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambdlambda-Ptase). The blot is identical ot the control except that it was incubated in lambdlambda-Ptase (1200 units for 30 min) before being exposed to the Anti-Phospho Ser549 synapsin I. The immunolabeling is completely eliminated by treatment with lambdlambda-Ptase.](http://images.novusbio.com/fullsize/Synapsin-I-[p-Ser549]-Antibody-Western-Blot-NB300-744-img0002.jpg "Western Blot: Synapsin I [p Ser549] Antibody [NB300-744] - Western blot of rat brain lysate showing specific immunolabeling of the ~78k synapsin I phosphorylated at Ser549 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambdlambda-Ptase). The blot is identical ot the control except that it was incubated in lambdlambda-Ptase (1200 units for 30 min) before being exposed to the Anti-Phospho Ser549 synapsin I. The immunolabeling is completely eliminated by treatment with lambdlambda-Ptase.")
![Immunohistochemistry: Synapsin I [p Ser549] Antibody [NB300-744] - Immunostaining of cultured mouse caudate neurons showing synapsin I when hosphorylated at Ser549.](http://images.novusbio.com/fullsize/Synapsin-I-[p-Ser549]-Antibody-Immunohistochemistry-NB300-744-img0003.jpg)
![Western Blot: CUGBP1/CELF1 Antibody (7A1-R) [NBP3-32179] - Western blot analysis of CUGBP1/CELF1 on different lysates with Mouse anti-CUGBP1/CELF1 antibody (NBP3-32179) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: 293T cell lysate Lane 3: NCI-H226 cell lysate Lane 4: COS-1 cell lysate Lane 5: Neuro-2a cell lysate Lane 6: NIH/3T3 cell lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 52 kDa Observed band size: 55 kDa Exposure time: 59 seconds; ECL; 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 (NBP3-32179) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32179_mouse-cugbp1-celf1-mab-7a1-r-27820241529558.jpg "Western Blot: CUGBP1/CELF1 Antibody (7A1-R) [NBP3-32179] - Western blot analysis of CUGBP1/CELF1 on different lysates with Mouse anti-CUGBP1/CELF1 antibody (NBP3-32179) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: 293T cell lysate Lane 3: NCI-H226 cell lysate Lane 4: COS-1 cell lysate Lane 5: Neuro-2a cell lysate Lane 6: NIH/3T3 cell lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 52 kDa Observed band size: 55 kDa Exposure time: 59 seconds; ECL; 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 (NBP3-32179) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CUGBP1/CELF1 Antibody (7A1-R) [NBP3-32179] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Mouse anti-CUGBP1/CELF1 antibody (NBP3-32179) at 1/1,000 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 (NBP3-32179) 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/nbp3-32179_mouse-cugbp1-celf1-mab-7a1-r-298202414115427.jpg)
![Immunocytochemistry/ Immunofluorescence: CUGBP1/CELF1 Antibody (7A1-R) [NBP3-32179] - Immunocytochemistry analysis of HeLa cells labeling CUGBP1/CELF1 with Mouse anti-CUGBP1/CELF1 antibody (NBP3-32179) 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-CUGBP1/CELF1 antibody (NBP3-32179) 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/nbp3-32179_mouse-cugbp1-celf1-mab-7a1-r-2920241192378.jpg)
![Western Blot: Androgen R/NR3C4 Antibody (PO00-29) [NBP3-32035] - Western blot analysis of Androgen R/NR3C4 on different lysates with Rabbit anti-Androgen R/NR3C4 antibody (NBP3-32035) at 1/1,000 dilution. Lane 1: A549 cell lysate Lane 2: K-562 cell lysate Lane 3: 22RV1 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 99 kDa Observed band size: 99/75 kDa Exposure time: 10 seconds; ECL; 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 (NBP3-32035) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32035_rabbit-androgen-r-nr3c4-mab-po00-29-278202415295545.jpg "Western Blot: Androgen R/NR3C4 Antibody (PO00-29) [NBP3-32035] - Western blot analysis of Androgen R/NR3C4 on different lysates with Rabbit anti-Androgen R/NR3C4 antibody (NBP3-32035) at 1/1,000 dilution. Lane 1: A549 cell lysate Lane 2: K-562 cell lysate Lane 3: 22RV1 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 99 kDa Observed band size: 99/75 kDa Exposure time: 10 seconds; ECL; 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 (NBP3-32035) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Androgen R/NR3C4 Antibody (PO00-29) [NBP3-32035] - Immunohistochemical analysis of paraffin-embedded human prostate carcinoma tissue with Rabbit anti-Androgen R/NR3C4 antibody (NBP3-32035) at 1/1,000 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 (NBP3-32035) 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/nbp3-32035_rabbit-androgen-r-nr3c4-mab-po00-29-298202413585515.jpg)
![Immunohistochemistry: Androgen R/NR3C4 Antibody (PO00-29) [NBP3-32035] - Immunofluorescence analysis of paraffin-embedded rat epididymis tissue labeling Androgen R/NR3C4 with Rabbit anti-Androgen R/NR3C4 antibody (NBP3-32035) at 1/50 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32035, green) at 1/50 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/nbp3-32035_rabbit-androgen-r-nr3c4-mab-po00-29-298202413585571.jpg)
![Immunocytochemistry/ Immunofluorescence: Androgen R/NR3C4 Antibody (PO00-29) [NBP3-32035] - Immunocytochemistry analysis of 22RV1 cells labeling Androgen R/NR3C4 with Rabbit anti-Androgen R/NR3C4 antibody (NBP3-32035) 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 Rabbit anti-Androgen R/NR3C4 antibody (NBP3-32035) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit 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-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32035_rabbit-androgen-r-nr3c4-mab-po00-29-2920241114836.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H4 [ac Lys13, ac Lys5, ac Lys8] Antibody [NBP2-59253] - Mouse NIH3T3 cells were stained with the antibody against H4K5,8,12,16ac and with DAPI. Cells were fixed with 4% formaldehyde for 10 minutes and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labeled with the H4K5,8,12,16ac antibody (left) diluted 1:500 in blocking solution followed by an anti- rabbit antibody conjugated to Alexa488. The middle panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.](http://images.novusbio.com/fullsize/Histone-H4-[ac-Lys13--ac-Lys5--ac-Lys8]-Antibody-Immunofluorescence-NBP2-59253-img0003.jpg "Immunocytochemistry/Immunofluorescence: Histone H4 [ac Lys13, ac Lys5, ac Lys8] Antibody [NBP2-59253] - Mouse NIH3T3 cells were stained with the antibody against H4K5,8,12,16ac and with DAPI. Cells were fixed with 4% formaldehyde for 10 minutes and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labeled with the H4K5,8,12,16ac antibody (left) diluted 1:500 in blocking solution followed by an anti- rabbit antibody conjugated to Alexa488. The middle panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.")
![Chromatin Immunoprecipitation: Histone H4 [ac Lys13, ac Lys5, ac Lys8] Antibody [NBP2-59253] - ChIP assays were performed using human HeLa cells, the antibody against H4K5,8,12,16ac and optimized PCR primer sets for qPCR. ChIP was performed with a ChIP- seq kit on sheared chromatin from 1 million cells. A titration of the antibody consisting of 1, 2, 5 and 10 ug per ChIP experiment was analysed. IgG (2 ug/IP) was used as negative IP control. QPCR was performed with primers for promoter of the active gene EIF4A2 and for a region 1 kb upstream of the GAPDH gene, used as positive controls, and for the inactive MYOD1 gene and the Sat2 satellite repeat region used as negative controls. Figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).](http://images.novusbio.com/fullsize/Histone-H4-[ac-Lys13--ac-Lys5--ac-Lys8]-Antibody-Chromatin-Immunoprecipitation-NBP2-59253-img0002.jpg)
![ELISA: Histone H4 [ac Lys13, ac Lys5, ac Lys8] Antibody [NBP2-59253] - To determine the titer of the antibody, an ELISA was performed using a serial dilution of the antibody directed against H4K5,8,12,16ac in antigen coated wells. The antigen used was a peptide containing the histone modification of interest. By plotting the absorbance against the antibody dilution, the titer of the antibody was estimated to be 1:21,200.](http://images.novusbio.com/fullsize/Histone-H4-[ac-Lys13--ac-Lys5--ac-Lys8]-Antibody-ELISA-NBP2-59253-img0001.jpg)
![Dot Blot: Histone H4 [ac Lys13, ac Lys5, ac Lys8] Antibody [NBP2-59253] - One hundred to 0.2 pmol of the respective peptides were spotted on a membrane. The antibody was used at a dilution of 1:20,000. Thr figure shows a high specificity of the antibody for the modification of interest.](http://images.novusbio.com/fullsize/Histone-H4-[ac-Lys13-ac-Lys5-ac-Lys8]-Antibody-Dot-Blot-NBP2-59253-img0004.jpg)
![Western Blot: ARHGAP22 [p Ser22] Antibody [NBP1-44072] - Lane 1: NIH3T3 cells transfected with a null vector. Lane 2: NIH3T3 cells transfected with ARHGAP22. Lane 3: NIH3T3 cells transfected with ARHGAP22 S22 to alanine mutation. Lane 4: NIH3T3 cells transfected with ARHGAP22 S397 to alanine mutation. Primary antibody: Left: ARHGAP22 pS22, Right: ARHGAP22 pS397 antibody at 1ug/mL for overnight at 4C. Secondary antibody: IRDye800 rabbit secondary antibody at 1:10,000 for 45 min at RT. Block: 5% BLOTTO O/N at 4C. Predicted/Observed size: 68 kDa for ARHGAP22. Other band(s): Unmodified ARHGAP22. ARHGAP22-pS22 antibody recognizes the S397>A mutation, not the S22>mutation; ARHGAP22 pS397 recognizes the pS22>A mutation, not the pS397>A mutation; Confirms the specificity of each ARHGAP22 phospho specific antibody.](http://images.novusbio.com/fullsize/ARHGAP22-[p-Ser22]-Antibody-Western-Blot-NBP1-44072-img0004.jpg "Western Blot: ARHGAP22 [p Ser22] Antibody [NBP1-44072] - Lane 1: NIH3T3 cells transfected with a null vector. Lane 2: NIH3T3 cells transfected with ARHGAP22. Lane 3: NIH3T3 cells transfected with ARHGAP22 S22 to alanine mutation. Lane 4: NIH3T3 cells transfected with ARHGAP22 S397 to alanine mutation. Primary antibody: Left: ARHGAP22 pS22, Right: ARHGAP22 pS397 antibody at 1ug/mL for overnight at 4C. Secondary antibody: IRDye800 rabbit secondary antibody at 1:10,000 for 45 min at RT. Block: 5% BLOTTO O/N at 4C. Predicted/Observed size: 68 kDa for ARHGAP22. Other band(s): Unmodified ARHGAP22. ARHGAP22-pS22 antibody recognizes the S397>A mutation, not the S22>mutation; ARHGAP22 pS397 recognizes the pS22>A mutation, not the pS397>A mutation; Confirms the specificity of each ARHGAP22 phospho specific antibody.")
![Western Blot: ARHGAP22 [p Ser22] Antibody [NBP1-44072] - ARHGAP22 [Phospo Ser22] Antibody [NBP1-44072] - Protein Molecular weight: 68 kDa Cell extracts from NIH 3T3cells that were transfected with either a null vector (CTRL), ARHGAP22, ARHGAP22-serine 22 to alanine mutation, ARHGAP22 serine 397 to alanine mutation were electroblotted. The left panel was probed with the NBP1-44072 antibody, while the right panel was probed with the NBP1-44073 antibody, each at 1ug/ml. Each antibody recognizes the unmodified ARHGAP22. NBP1-44072 antibody recognized the S397-A mutation but not the S22-A mutation, while NBP1-44073 antibody recognizes the pS22-A mutation and not the pS397-A mutation. This data confirms the specificity of each ARHGAP22 phospho specific antibody.](http://images.novusbio.com/fullsize/ARHGAP22-[p-Ser22]-Antibody-Western-Blot-NBP1-44072-img0001.jpg)
![Western Blot: eIF2 alpha/EIF2S1 Antibody [NB100-2249] - Detection of Human and Mouse eIF2-alpha on HeLa whole cell lysate using NB100-2249.](http://images.novusbio.com/fullsize/eIF2-alpha-EIF2S1-Antibody-Western-Blot-NB100-2249-img0001.jpg "Western Blot: eIF2 alpha/EIF2S1 Antibody [NB100-2249] - Detection of Human and Mouse eIF2-alpha on HeLa whole cell lysate using NB100-2249.")
![Immunohistochemistry-Paraffin: eIF2 alpha/EIF2S1 Antibody [NB100-2249] - Human colon carcinoma (left) and mouse teratoma (right). Antibody: Affinity purified rabbit anti-eIF2alpha/EIF2S1 used at a dilution of 1:1,000 (0.2ug/ml) and 1:200 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/eIF2-alpha-EIF2S1-Antibody-Immunohistochemistry-Paraffin-NB100-2249-img0003.jpg)
![Western Blot: ASAP1 Antibody [NBP2-24643] - Analysis of ASAP1 in mouse brain lysate in the 1) absence and 2) presence of immunizing peptide using NBP2-24643 at 2.0 ug/ml. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/ASAP1-Antibody-Western-Blot-NBP2-24643-img0001.jpg "Western Blot: ASAP1 Antibody [NBP2-24643] - Analysis of ASAP1 in mouse brain lysate in the 1) absence and 2) presence of immunizing peptide using NBP2-24643 at 2.0 ug/ml. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")
![Western Blot: ARHGAP22 [p Ser397] Antibody [NBP1-44073] - Lane 1: NIH3T3 cells transfected with a null vector. Lane 2: NIH3T3 cells transfected with ARHGAP22. Lane 3: NIH3T3 cells transfected with ARHGAP22 S22 to alanine mutation. Lane 4: NIH3T3 cells transfected with ARHGAP22 S397 to alanine mutation. Primary antibody: Left: ARHGAP22 pS22, Right: ARHGAP22 pS397 antibody at 1ug/mL for overnight at 4C. Secondary antibody: IRDye800 rabbit secondary antibody at 1:10,000 for 45 min at RT. Block: 5% BLOTTO O/N at 4C. Predicted/Observed size: 68 kDa for ARHGAP22. Other band(s): Unmodified ARHGAP22. ARHGAP22-pS22 antibody recognizes the S397>A mutation, not the S22>mutation; ARHGAP22 pS397 recognizes the pS22>A mutation, not the pS397>A mutation; Confirms the specificity of each ARHGAP22 phospho specific antibody.](http://images.novusbio.com/fullsize/ARHGAP22 [p Ser397] Antibody-Western Blot-NBP1-44073-img0004.jpg "Western Blot: ARHGAP22 [p Ser397] Antibody [NBP1-44073] - Lane 1: NIH3T3 cells transfected with a null vector. Lane 2: NIH3T3 cells transfected with ARHGAP22. Lane 3: NIH3T3 cells transfected with ARHGAP22 S22 to alanine mutation. Lane 4: NIH3T3 cells transfected with ARHGAP22 S397 to alanine mutation. Primary antibody: Left: ARHGAP22 pS22, Right: ARHGAP22 pS397 antibody at 1ug/mL for overnight at 4C. Secondary antibody: IRDye800 rabbit secondary antibody at 1:10,000 for 45 min at RT. Block: 5% BLOTTO O/N at 4C. Predicted/Observed size: 68 kDa for ARHGAP22. Other band(s): Unmodified ARHGAP22. ARHGAP22-pS22 antibody recognizes the S397>A mutation, not the S22>mutation; ARHGAP22 pS397 recognizes the pS22>A mutation, not the pS397>A mutation; Confirms the specificity of each ARHGAP22 phospho specific antibody.")
![Western Blot: ARHGAP22 [p Ser397] Antibody [NBP1-44073] - Western Blot: ARHGAP22 [Phospo Ser22] Antibody [NBP1-44072] - Protein Molecular weight: 68 kDa Cell extracts from NIH 3T3cells that were transfected with either a null vector (CTRL), ARHGAP22, ARHGAP22-serine 22 to alanine mutation, ARHGAP22 serine 397 to alanine mutation were electroblotted. The left panel was probed with the NBP1-44072 antibody, while the right panel was probed with the NBP1-44073 antibody, each at 1ug/ml. Each antibody recognizes the unmodified ARHGAP22. NBP1-44072 antibody recognized the S397->A mutation but not the S22->A mutation, while NBP1-44073 antibody recognizes the pS22->A mutation and not the pS397->A mutation. This data confirms the specificity of each ARHGAP22 phospho specific antibody.](http://images.novusbio.com/fullsize/ARHGAP22-[p-Ser397]-Antibody-Western-Blot-NBP1-44073-img0001.jpg)
![Immunohistochemistry: STK4 Antibody [NB110-39128] - Sample: FFPE section of human placenta. Antibody: Affinity purified rabbit anti- MST1/2 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/STK4-Antibody-Immunohistochemistry-NB110-39128-img0003.jpg "Immunohistochemistry: STK4 Antibody [NB110-39128] - Sample: FFPE section of human placenta. Antibody: Affinity purified rabbit anti- MST1/2 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB")
![Immunoprecipitation: STK4 Antibody [NB110-39128] - Detection of MST1 and MST2 on HeLa whole cell lysate using NB110-39128. MST1 and MST2 were simultaneously IPed using other MST1/2 antibodies.](http://images.novusbio.com/fullsize/STK4-Antibody-Immunoprecipitation-NB110-39128-img0001.jpg)
![Western Blot: alpha Adducin Antibody [NBP2-15359] - A. 30 ug Jurkat whole cell lysate/extract B. 30 ug Raji whole cell lysate/extract C. 30 ug NCI-H929 whole cell lysate/extract 7.5 % SDS-PAGE alpha Adducin antibody [N1N2], N-term dilution: 1:1000](http://images.novusbio.com/fullsize/alpha-Adducin-Antibody-Western-Blot-NBP2-15359-img0003.jpg "Western Blot: alpha Adducin Antibody [NBP2-15359] - A. 30 ug Jurkat whole cell lysate/extract B. 30 ug Raji whole cell lysate/extract C. 30 ug NCI-H929 whole cell lysate/extract 7.5 % SDS-PAGE alpha Adducin antibody [N1N2], N-term dilution: 1:1000")
![Immunohistochemistry-Paraffin: alpha Adducin Antibody [NBP2-15359] - Paraffin-embedded SG xenograft, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/alpha-Adducin-Antibody-Immunohistochemistry-Paraffin-NBP2-15359-img0001.jpg)
![Western Blot: alpha Adducin Antibody [NBP2-15359] - Sample (50 ug of whole cell lysate) A: mouse liver 7.5% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/alpha-Adducin-Antibody-Western-Blot-NBP2-15359-img0002.jpg)
![Immunohistochemistry: alpha Adducin Antibody [NBP2-15359] - alpha Adducin antibody [N1N2], N-term detects alpha Adducin protein at nucleus on whole-mount zebrafish embryos by immunohistochemical analysis. Sample: Paraformaldehyde-fixed zebrafish embryos. alpha Adducin antibody [N1N2], N-term (NBP2-15359) dilution: 1:200.](http://images.novusbio.com/fullsize/nbp2-15359_rabbit-polyclonal-alpha-adducin-antibody-91020242011482.jpg)
![Western Blot: STXBP1 Antibody [NBP2-20526] - Sample (30 ug of whole cell lysate) A: 293T B: A431 7. 5% SDS PAGE gel, diluted at 1:3000.](http://images.novusbio.com/fullsize/STXBP1-Antibody-Western-Blot-NBP2-20526-img0002.jpg "Western Blot: STXBP1 Antibody [NBP2-20526] - Sample (30 ug of whole cell lysate) A: 293T B: A431 7. 5% SDS PAGE gel, diluted at 1:3000.")
![Immunocytochemistry/Immunofluorescence: STXBP1 Antibody [NBP2-20526] - Confocal immunofluorescence analysis of methanol-fixed A431, using STXBP1 antibody (Green) at 1:500 dilution. Alpha-tubulin filaments are labeled with Alpha-tubulin antibody (Red) at 1:2000.](http://images.novusbio.com/fullsize/STXBP1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-20526-img0003.jpg)
![Western Blot: Syntaxin-BP1 Antibody [NBP2-20526] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Syntaxin-BP1 antibody (NBP2-20526) diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-20526_rabbit-polyclonal-syntaxin-bp1-antibody-91020242011477.jpg)
![Munc18-1 antibody detects Munc18-1 protein by immunofluorescent analysis.Sample: DIV9 rat E18 primary cortical neurons were fixed in 4% paraformaldehyde at RT for 15 min.Green: Munc18-1 protein stained by Munc18-1 antibody (NBP2-20526) diluted at 1:500.Red: beta Tubulin 3/ Tuj1, stained by beta Tubulin 3/ Tuj1 antibody [GT886] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp2-20526_rabbit-polyclonal-syntaxin-bp1-antibody-immunocytochemistry-immunofluorescence-2611202518315416.jpg)
![Western Blot: ATP Citrate Lyase Antibody [NBP1-33430] - Sample (30 ug of whole cell lysate) A: Hela B: Raji 7. 5% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/ATP-Citrate-Lyase-Antibody-Western-Blot-NBP1-33430-img0005.jpg "Western Blot: ATP Citrate Lyase Antibody [NBP1-33430] - Sample (30 ug of whole cell lysate) A: Hela B: Raji 7. 5% SDS PAGE; antibody diluted at 1:1000.")
![Immunocytochemistry/Immunofluorescence: ATP Citrate Lyase Antibody [NBP1-33430] - HeLa cells were fixed in ice-cold MeOH for 5 min. Green: ATP citrate lyase protein stained by ATP citrate lyase antibody [C2C3], C-term diluted at 1:200. Blue: Hoechst 33342 staining.](http://images.novusbio.com/fullsize/ATP-Citrate-Lyase-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-33430-img0006.jpg)
![Western Blot: ATP Citrate Lyase Antibody [NBP1-33430] - Sample (50 ug of whole cell lysate) A: mouse brain 5% SDS PAGE, antibody diluted at 1:2000.](http://images.novusbio.com/fullsize/ATP-Citrate-Lyase-Antibody-Western-Blot-NBP1-33430-img0003.jpg)
![Western Blot: ATP Citrate Lyase Antibody [NBP1-33430] - A. 30 ug PC-12 whole cell lysate/extract, B. 30 ug Rat 2 whole cell lysate/extract 5% SDS-PAGE gel, antibody dilution 1:1000.](http://images.novusbio.com/fullsize/ATP-Citrate-Lyase-Antibody-Western-Blot-NBP1-33430-img0004.jpg)