| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-48512-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-57700-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-54748-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-79877 | |||
![Immunohistochemistry-Paraffin-NBP3-21454-Tau [p Ser396] Antibody (SN62-09)-Rat brain tissue using NBP3-21454. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/antibody/nbp3-21454_rabbit-tau-p-ser396-mab-sn62-09-immunohistochemistry-paraffin-16820239811.jpg "Immunohistochemistry-Paraffin-NBP3-21454-Tau [p Ser396] Antibody (SN62-09)-Rat brain tissue using NBP3-21454. Counter stained with hematoxylin.")
![Immunohistochemistry-Paraffin: Tau [p Ser396] Antibody (SN62-09) [NBP3-21454] - Mouse brain tissue using NBP3-21454. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/antibody/nbp3-21454_rabbit-tau-p-ser396-mab-sn62-09-immunohistochemistry-paraffin-16820239936.jpg)
![Immunocytochemistry/ Immunofluorescence: Tau [p Ser396] Antibody (SN62-09) [NBP3-21454] - Immunocytochemical analysis of Tau [p Ser396] in PC12 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/nbp3-21454_rabbit-tau-p-ser396-mab-sn62-09-103202523464548.jpg)
![Immunocytochemistry/ Immunofluorescence: Tau [p Ser396] Antibody (SN62-09) [NBP3-21454] - Immunocytochemical analysis of Tau [p Ser396] in N2A cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/nbp3-21454_rabbit-tau-p-ser396-mab-sn62-09-103202523464554.jpg)
![Immunohistochemistry-Paraffin: LC3A Antibody [NBP2-48512] - Staining in human cerebral cortex and pancreas tissues using anti-MAP1LC3A antibody. Corresponding MAP1LC3A RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/LC3A-Antibody-Immunohistochemistry-Paraffin-NBP2-48512-img0005.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: LC3A Antibody [NBP2-48512] - Staining in human cerebral cortex and pancreas tissues using anti-MAP1LC3A antibody. Corresponding MAP1LC3A RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Western Blot: LC3A Antibody [NBP2-48512] - Analysis in control (vector only transfected HEK293T lysate) and MAP1LC3A over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).](http://images.novusbio.com/fullsize/LC3A-Antibody-Western-Blot-NBP2-48512-img0006.jpg)
![Western Blot: LC3A Antibody [NBP2-48512] - Analysis in human cerebral cortex tissue.](http://images.novusbio.com/fullsize/LC3A-Antibody-Western-Blot-NBP2-48512-img0003.jpg)
![Immunohistochemistry-Paraffin: LC3A Antibody [NBP2-48512] - Staining of human cerebral cortex shows strong cytoplasmic and nuclear positivity in neuronal cells.](http://images.novusbio.com/fullsize/LC3A-Antibody-Immunohistochemistry-Paraffin-NBP2-48512-img0001.jpg)
![Immunohistochemistry-Paraffin: LC3A Antibody [NBP2-48512] - Staining of human pancreas shows low expression as expected.](http://images.novusbio.com/fullsize/LC3A-Antibody-Immunohistochemistry-Paraffin-NBP2-48512-img0004.jpg)
![Western Blot: Rabbit Tau [p Thr181] mAb (HL2498) [NBP3-45158] - Untreated (–) and treated (+) SK-N-SH whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Tau (p Thr181) antibody [HL2498] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-45158_rabbit-tau-p-thr181-mab-hl2498-azide-and-bsa-free-western-blot-152025102720.jpg "<b>Biological Strategies Validation and Genetic Strategies Validation.</b>Western Blot: Rabbit Tau [p Thr181] mAb (HL2498) [NBP3-45158] - Untreated (–) and treated (+) SK-N-SH whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Tau (p Thr181) antibody [HL2498] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![<b>Biological Strategies Validation and Genetic Strategies Validation.</b>Western Blot: Rabbit Tau [p Thr181] mAb (HL2498) [NBP3-45158] - Untreated (–) and treated (+) Mouse tissue extract (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Tau (p Thr181) antibody [HL2498] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-45158_rabbit-tau-p-thr181-mab-hl2498-azide-and-bsa-free-western-blot-152025103434..jpg)
![Immunohistochemistry: Rabbit Tau [p Thr181] mAb (HL2498) [NBP3-45158] - Tau (p Thr181) antibody [HL2498] detects Tau (phospho Thr181) protein in the cytoplasm by immunohistochemical analysis in the presence of non phospho control peptide (left) but not in the presence of the antigenic phospho peptide (right).Sample: Paraffin-embedded mouse brain.Tau (p Thr181) stained by Tau (p Thr181) antibody [HL2498] diluted at 1:100.](http://images.novusbio.com/fullsize/nbp3-45158_rabbit-tau-p-thr181-mab-hl2498-azide-and-bsa-free-immunohistochemistry-152025103033..jpg)
![ELISA: Rabbit Tau [p Thr181] mAb (HL2498) [NBP3-45158] - Sandwich ELISA detection of Tau peptide and Tau (phospho Thr181) peptide using antibodies as below.Capture: Tau (phospho Thr181) antibody [HL2498] (NBP3-45158) (5 ug/mL)Detection: HRP-conjugated Tau (phospho Thr181) antibody [HL2497] (NBP3-45157) (1 ug/mL)](http://images.novusbio.com/fullsize/nbp3-45158_rabbit-tau-p-thr181-mab-hl2498-azide-and-bsa-free-elisa-152025104331..jpg)
![ELISA: Rabbit Tau [p Thr181] mAb (HL2498) - Sandwich ELISA detection of Tau peptide and Tau (p Thr181) peptide using antibodies as below.Capture: Tau (p Thr181) antibody [HL2497] (NBP3-45157) (5 ug/mL)Detection: HRP-conjugated Tau (p Thr181) antibody [HL2498] (NBP3-45158) (1 ug/mL)](http://images.novusbio.com/fullsize/nbp3-45158_rabbit-tau-p-thr181-mab-hl2498-azide-and-bsa-free-elisa-152025105927..jpg)
![Western Blot: Pax2 Antibody (JJ082-08) [NBP2-67849] - Analysis of Pax2 on human kidney tissue lysates with Rabbit anti-Pax2 antibody at 1/500 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 45 kDa Observed band size: 45 kDa Exposure time: 2 minutes; 10% 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 1/500 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/Pax2-Antibody-JJ082-08-Western-Blot-NBP2-67849-img0003.jpg "Western Blot: Pax2 Antibody (JJ082-08) [NBP2-67849] - Analysis of Pax2 on human kidney tissue lysates with Rabbit anti-Pax2 antibody at 1/500 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 45 kDa Observed band size: 45 kDa Exposure time: 2 minutes; 10% 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 1/500 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.")
![Immunohistochemistry-Paraffin: Pax2 Antibody (JJ082-08) [NBP2-67849] - Analysis of paraffin-embedded rat epididymis tissue with Rabbit anti-Pax2 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 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/Pax2-Antibody-JJ082-08-Immunohistochemistry-Paraffin-NBP2-67849-img0005.jpg)
![Western Blot: Pax2 Antibody (JJ082-08) [NBP2-67849] - Western blot analysis of Pax2 on human kidney tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat](http://images.novusbio.com/fullsize/Pax2-Antibody-JJ082-08-Western-Blot-NBP2-67849-img0002.jpg)
![Immunohistochemistry-Paraffin: Pax2 Antibody (JJ082-08) [NBP2-67849] - Analysis of paraffin-embedded human kidney tissue using anti-Pax2 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Pax2-Antibody-JJ082-08-Immunohistochemistry-Paraffin-NBP2-67849-img0001.jpg)
![Immunohistochemistry-Paraffin: Pax2 Antibody (JJ082-08) [NBP2-67849] - Analysis of paraffin-embedded human kidney tissue with Rabbit anti-Pax2 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/400 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/Pax2-Antibody-JJ082-08-Immunohistochemistry-Paraffin-NBP2-67849-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: Pax2 Antibody [NBP2-57700] - Staining of human cell line U-2 OS shows localization to nucleoli. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/Pax2-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-57700-img0001.jpg "Immunocytochemistry/Immunofluorescence: Pax2 Antibody [NBP2-57700] - Staining of human cell line U-2 OS shows localization to nucleoli. Antibody staining is shown in green.")
![Immunohistochemistry-Paraffin: Pax2 Antibody [NBP2-57700] - Staining of human epididymis shows high expression.](http://images.novusbio.com/fullsize/Pax2-Antibody-Immunohistochemistry-Paraffin-NBP2-57700-img0003.jpg)
![Immunohistochemistry-Paraffin: Pax2 Antibody [NBP2-57700] -Staining of human skeletal muscle shows no positivity in myocytes as expected.](http://images.novusbio.com/fullsize/antibody/nbp2-57700_rabbit-polyclonal-pax2-antibody-immunohistochemistry-paraffin-1142024122412..jpg)
![Immunohistochemistry-Paraffin: GFAP Antibody [NBP2-54748] - Analysis in human cerebral cortex and pancreas tissues using Anti-GFAP antibody. Corresponding GFAP RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/GFAP-Antibody-Immunohistochemistry-Paraffin-NBP2-54748-img0004.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: GFAP Antibody [NBP2-54748] - Analysis in human cerebral cortex and pancreas tissues using Anti-GFAP antibody. Corresponding GFAP RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: GFAP Antibody [NBP2-54748] - Staining of human pancreas shows low expression as expected.](http://images.novusbio.com/fullsize/GFAP-Antibody-Immunohistochemistry-Paraffin-NBP2-54748-img0006.jpg)
![Immunohistochemistry-Paraffin: GFAP Antibody [NBP2-54748] - Staining of human cerebral cortex shows high expression.](http://images.novusbio.com/fullsize/GFAP-Antibody-Immunohistochemistry-Paraffin-NBP2-54748-img0005.jpg)
![ELISA: Tau [p Thr217] Antibody [NBP3-13481] - Indirect ELISA analysis performed by coating plate with recombinant partial Tau peptide and Tau (phospho Thr217) peptide (1000-0.003 ng/mL). Coated protein was probed with Tau (phospho Thr217) antibody (NBP3-13481) (1 ug/mL). Goat anti-rabbit IgG antibody (HRP) (NBP2-19301) (1:10000) was used to detect bound primary antibody.](http://images.novusbio.com/fullsize/Tau-[p-Thr217]-Antibody-ELISA-NBP3-13481-img0002.jpg "ELISA: Tau [p Thr217] Antibody [NBP3-13481] - Indirect ELISA analysis performed by coating plate with recombinant partial Tau peptide and Tau (phospho Thr217) peptide (1000-0.003 ng/mL). Coated protein was probed with Tau (phospho Thr217) antibody (NBP3-13481) (1 ug/mL). Goat anti-rabbit IgG antibody (HRP) (NBP2-19301) (1:10000) was used to detect bound primary antibody.")
![IHC-P-Tau [p Thr217] Antibody-Rat brain. Tau (phospho Thr217) stained by Tau (phospho Thr217) antibody diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/antibody/nbp3-13481_rabbit-tau-p-thr-217-pab-immunohistochemistry-paraffin-89202384342..jpg)
![Tau (phospho Thr217) antibody detects Tau (phospho Thr217) protein at nucleus and cytoskeleton by immunofluorescent analysis.Sample: DIV9 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: Tau (phospho Thr217) stained by Tau (phospho Thr217) antibody (NBP3-13481) 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/nbp3-13481_rabbit-tau-p-thr-217-pab-immunocytochemistry-immunofluorescence-2611202518274612.jpg)
![Western Blot: HSP90 alpha Antibody (0R3S6) [NBP3-16528] - Western blot analysis of extracts of various cell lines, using HSP90 alpha Rabbit mAb (NBP3-16528) 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: 3s.](http://images.novusbio.com/fullsize/HSP90-alpha-Antibody-0R3S6-Western-Blot-NBP3-16528-img0001.jpg "Western Blot: HSP90 alpha Antibody (0R3S6) [NBP3-16528] - Western blot analysis of extracts of various cell lines, using HSP90 alpha Rabbit mAb (NBP3-16528) 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: 3s.")
![Immunoprecipitation: HSP90 alpha Antibody (0R3S6) [NBP3-16528] - Immunoprecipitation analysis of 300ug extracts of 293T cells using 3ug HSP90 alpha antibody (NBP3-16528). Western blot was performed from the immunoprecipitate using HSP90 alpha antibody (NBP3-16528) at a dilition of 1:1000.](http://images.novusbio.com/fullsize/HSP90-alpha-Antibody-0R3S6-Immunoprecipitation-NBP3-16528-img0002.jpg)
![Immunocytochemistry/ Immunofluorescence: HSP90 alpha Antibody (0R3S6) [NBP3-16528] - Confocal imaging of paraffin-embedded Rat brain tissue using HSP90 alpha Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . DAPI was used for nuclear staining (Blue). Microwave antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.](http://images.novusbio.com/fullsize/nbp3-16528_rabbit-hsp90-alpha-mab-0r3s6-52202511411441.jpg)
![Immunocytochemistry/ Immunofluorescence: HSP90 alpha Antibody (0R3S6) [NBP3-16528] - Confocal imaging of paraffin-embedded Mouse brain tissue using HSP90 alpha Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . DAPI was used for nuclear staining (Blue). Microwave antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.](http://images.novusbio.com/fullsize/nbp3-16528_rabbit-hsp90-alpha-mab-0r3s6-52202511402778.jpg)
![Immunocytochemistry/ Immunofluorescence: HSP90 alpha Antibody (0R3S6) [NBP3-16528] - Confocal imaging of paraffin-embedded Human colon cancer tissue using HSP90 alpha Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.](http://images.novusbio.com/fullsize/nbp3-16528_rabbit-hsp90-alpha-mab-0r3s6-5220251255590.jpg)
![Immunohistochemistry-Paraffin: Pax2 Antibody (PAX2/1104) [NBP2-79742] - Formalin-fixed, paraffin-embedded human Renal Cell Carcinoma stained with Pax2 Antibody (PAX2/1104).](http://images.novusbio.com/fullsize/Pax2-Antibody-PAX2-1104-Immunohistochemistry-Paraffin-NBP2-79742-img0003.jpg "Immunohistochemistry-Paraffin: Pax2 Antibody (PAX2/1104) [NBP2-79742] - Formalin-fixed, paraffin-embedded human Renal Cell Carcinoma stained with Pax2 Antibody (PAX2/1104).")
![Immunohistochemistry-Paraffin: Pax2 Antibody (PAX2/1104) [NBP2-79742] - Formalin-fixed, paraffin-embedded human Colon Carcinoma stained with Pax2 Antibody (PAX2/1104).](http://images.novusbio.com/fullsize/Pax2-Antibody-PAX2-1104-Immunohistochemistry-Paraffin-NBP2-79742-img0001.jpg)
![Immunohistochemistry-Paraffin: Pax2 Antibody (PAX2/1104) [NBP2-79742] - Formalin-fixed, paraffin-embedded human Ovarian Carcinoma stained with Pax2 Antibody (PAX2/1104).](http://images.novusbio.com/fullsize/Pax2-Antibody-PAX2-1104-Immunohistochemistry-Paraffin-NBP2-79742-img0002.jpg)
![Protein Array: Pax2 Antibody (PAX2/1104) [NBP2-79742] - Analysis of Protein Array containing more than 19,000 full-length human proteins using Pax2 Antibody (PAX2/1104). Z- and S- Score: The Z-score represents the strength of a signal that a monoclonal antibody (MAb) (in combination with a fluorescently-tagged anti-IgG secondary antibody) produces when binding to a particular protein on the HuProt(TM) array. Z-scores are described in units of standard deviations (SD's) above the mean value of all signals generated on that array. If targets on HuProt(TM) are arranged in descending order of the Z-score, the S-score is the difference (also in units of SD's) between the Z-score. S-score therefore represents the relative target specificity of a MAb to its intended target. A MAb is considered to specific to its intended target, if the MAb has an S-score of at least 2.5.](http://images.novusbio.com/fullsize/Pax2-Antibody-PAX2-1104-Protein-Array-NBP2-79742-img0004.jpg)
![Western Blot: Rabbit Tau mAb (HL2982) [NBP3-45159] - Whole cell extract (30 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-45159_rabbit-tau-mab-hl2982-azide-and-bsa-free-western-blot-152025112952..jpg "Western Blot: Rabbit Tau mAb (HL2982) [NBP3-45159] - Whole cell extract (30 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Western Blot: Rabbit Tau mAb (HL2982) [NBP3-45159] - Various tissue extracts (50 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-45159_rabbit-tau-mab-hl2982-azide-and-bsa-free-western-blot-15202511328..jpg)
![Western Blot: Rabbit Tau mAb (HL2982) - Various tissue extracts (50 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-45159_rabbit-tau-mab-hl2982-azide-and-bsa-free-western-blot-15202511382..jpg)
![<b>Orthogonal Strategies Validation. </b>Western Blot: Rabbit Tau mAb (HL2982) [NBP3-45159] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based.](http://images.novusbio.com/fullsize/nbp3-45159_rabbit-tau-mab-hl2982-azide-and-bsa-free-western-blot-152025115512..jpg)
![Western Blot: Tau [p Ser 202, p Thr 205] Antibody (AH36) [NBP3-18265] - Western Blot analysis of Human iPSC-derived cortical neurons showing detection of Tau protein using Rabbit Anti-Tau Monoclonal Antibody, Clone AH36 (NBP3-18265). Lane 1: MW ladder. Lane 2: Control (non-disease) line. Lane 2: Ex10+16 tau mutant sample. Lane 3: P301L tau mutant sample. Load: 50ug. Primary Antibody: Rabbit Anti-Tau Monoclonal Antibody (NBP3-18265) at 1:500 for Overnight. pSer202/pThr205 was detected using NBP3-18265. Total tau was detected using mouse anti-tau antibody (clone HT7). The bar graph on the right shows quantification of pSer202/pThr205 compared to total tau in each sample.](http://images.novusbio.com/fullsize/Tau-p-Ser-202-p-Thr-205-Antibody-AH36-Western-Blot-NBP3-18265-img0002.jpg "Western Blot: Tau [p Ser 202, p Thr 205] Antibody (AH36) [NBP3-18265] - Western Blot analysis of Human iPSC-derived cortical neurons showing detection of Tau protein using Rabbit Anti-Tau Monoclonal Antibody, Clone AH36 (NBP3-18265). Lane 1: MW ladder. Lane 2: Control (non-disease) line. Lane 2: Ex10+16 tau mutant sample. Lane 3: P301L tau mutant sample. Load: 50ug. Primary Antibody: Rabbit Anti-Tau Monoclonal Antibody (NBP3-18265) at 1:500 for Overnight. pSer202/pThr205 was detected using NBP3-18265. Total tau was detected using mouse anti-tau antibody (clone HT7). The bar graph on the right shows quantification of pSer202/pThr205 compared to total tau in each sample.")
![Immunocytochemistry/Immunofluorescence: Tau [p Ser 202, p Thr 205] Antibody (AH36) [NBP3-18265] - Immunocytochemistry/Immunofluorescence analysis using Rabbit Anti-Tau Monoclonal Antibody, Clone AH36 (NBP3-18265). Tissue: iPSC-derived cortical excitatory neurons. Species: Human. Primary Antibody: Rabbit Anti-Tau Monoclonal Antibody (NBP3-18265) at 1:500 for Overnight. Secondary Antibody: Donkey anti-rabbit: Alexa Fluor 488 at 1:1000. Counterstain: DAPI. A) iPSC-derived neurons from non-demented control (NDC). B) iPSC-derived neurons from subject with P301L MAPT mutation. Images acquired using an automated Opera Phoenix system. Each field of view is a max projection from 10 planes of 1 um stacks.](http://images.novusbio.com/fullsize/Tau-p-Ser-202-p-Thr-205-Antibody-AH36-Immunocytochemistry-Immunofluorescence-NBP3-18265-img0001.jpg)
![Dot Blot: Tau [p Ser 202, p Thr 205] Antibody (AH36) [NBP3-18265] - Dot Blot analysis using Rabbit Anti-Tau Monoclonal Antibody, Clone AH36 (NBP3-18265). Species: E. Coli, Baculovirus. Primary Antibody: Rabbit Anti-Tau Monoclonal Antibody (NBP3-18265) at 1:500. Secondary Antibody: Goat anti-rabbit IgG:HRP.](http://images.novusbio.com/fullsize/Tau-p-Ser-202-p-Thr-205-Antibody-AH36-Dot-Blot-NBP3-18265-img0003.jpg)
![Western Blot: HSP70/HSPA1A Antibody (5U9A0) [NBP3-16482] - Western blot analysis of extracts of various cell lines, using HSP70/HSPA1A Rabbit mAb (NBP3-16482) 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/HSP70-HSPA1A-Antibody-5U9A0-Western-Blot-NBP3-16482-img0003.jpg "Western Blot: HSP70/HSPA1A Antibody (5U9A0) [NBP3-16482] - Western blot analysis of extracts of various cell lines, using HSP70/HSPA1A Rabbit mAb (NBP3-16482) 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.")
![Immunocytochemistry/Immunofluorescence: HSP70/HSPA1A Antibody (5U9A0) [NBP3-16482] - Immunofluorescence analysis of NIH-3T3 cells using HSP70/HSPA1A Rabbit mAb (NBP3-16482) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/HSP70-HSPA1A-Antibody-5U9A0-Immunocytochemistry-Immunofluorescence-NBP3-16482-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: HSP70/HSPA1A Antibody (5U9A0) [NBP3-16482] - Immunofluorescence analysis of HeLa cells using HSP70/HSPA1A Rabbit mAb (NBP3-16482) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/HSP70-HSPA1A-Antibody-5U9A0-Immunocytochemistry-Immunofluorescence-NBP3-16482-img0001.jpg)