| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-06705SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-27073SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-56554SS | |||
| Azide and BSA Free | NBP2-80914 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-33068 | |||
![Immunocytochemistry/Immunofluorescence: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Analysis of methanol-fixed HeLa, using DCTN1 antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with an alpha Tubulin antibody (Red) at 1:2000.](http://images.novusbio.com/fullsize/Dynactin-Subunit-1-DCTN1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-30880-img0007.jpg "Immunocytochemistry/Immunofluorescence: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Analysis of methanol-fixed HeLa, using DCTN1 antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with an alpha Tubulin antibody (Red) at 1:2000.")
![Immunohistochemistry-Paraffin: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Paraffin-embedded Rat brain. DCTN1 antibody [C3], C-term diluted at 1:500.](http://images.novusbio.com/fullsize/Dynactin-Subunit-1-DCTN1-Antibody-Immunohistochemistry-Paraffin-NBP1-30880-img0011.jpg)
![Western Blot: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Various tissue extracts (50 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DCTN1 antibody [C3], C-term diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Dynactin-Subunit-1-DCTN1-Antibody-Western-Blot-NBP1-30880-img0013.jpg)
![Western Blot: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DCTN1 antibody [C3], C-term diluted at 1:2500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Dynactin-Subunit-1-DCTN1-Antibody-Western-Blot-NBP1-30880-img0015.jpg)
![Western Blot: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with DCTN1 antibody [C3], C-term diluted at 1:2500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Dynactin-Subunit-1-DCTN1-Antibody-Western-Blot-NBP1-30880-img0017.jpg)
![Immunohistochemistry-Paraffin: Dynactin Subunit 1/DCTN1 Antibody [NBP1-30880] - Paraffin-embedded OVCA, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/Dynactin-Subunit-1-DCTN1-Antibody-Immunohistochemistry-Paraffin-NBP1-30880-img0008.jpg)
![Various tissue extracts (50 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Dynactin Subunit 1/DCTN1 antibody [C3], C-term (NBP1-30880) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp1-30880_rabbit-polyclonal-dynactin-subunit-1-dctn1-antibody-western-blot-141120251842522.jpg)
![Western Blot: Nbs1 Antibody [NBP1-06705] - Western Blot analysis of Nbs1 on NIH/3T3 (Lane 6) and HeLa whole cell extract (Lane 7) with Nbs1 Antibody [NBP1-06705]. Observed molecular weight at ~99 kDa.](http://images.novusbio.com/fullsize/NBS1-Antibody-Western-Blot-NBP1-06705-img0004.jpg "Western Blot: Nbs1 Antibody [NBP1-06705] - Western Blot analysis of Nbs1 on NIH/3T3 (Lane 6) and HeLa whole cell extract (Lane 7) with Nbs1 Antibody [NBP1-06705]. Observed molecular weight at ~99 kDa.")
![Immunohistochemistry-Paraffin: Nbs1 Antibody [NBP1-06705] - Staining of paraffin-embedded mouse skin with Nbs1 Antibody [NBP1-06705].](http://images.novusbio.com/fullsize/NBS1-Antibody-Immunohistochemistry-Paraffin-NBP1-06705-img0003.jpg)
![Western Blot: FABP7/B-FABP Antibody [NBP2-27073] - Analysis of FABP7 in human spleen in the 1) absence and 2) presence of immunizing peptide, 3) mouse spleen, and 4) mouse embryonic brain lysate using this antibody. goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/FABP7-B-FABP-Antibody-Western-Blot-NBP2-27073-img0004.jpg "Western Blot: FABP7/B-FABP Antibody [NBP2-27073] - Analysis of FABP7 in human spleen in the 1) absence and 2) presence of immunizing peptide, 3) mouse spleen, and 4) mouse embryonic brain lysate using this antibody. goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")
![Immunohistochemistry-Paraffin: FABP7/B-FABP Antibody [NBP2-27073] - Analysis of FABP7 in formalin-fixed, paraffin-embedded human brain tissue using this antibody at 5 ug/ml.](http://images.novusbio.com/fullsize/FABP7-B-FABP-Antibody-Immunohistochemistry-Paraffin-NBP2-27073-img0003.jpg)
![Western Blot: EGFR Antibody [NB100-596] - NPM1 knockdown decreases EGF expression. NPM1 controls activation of the EGF/EGFR pathway downstream effectors. Proteins, extracted from shScr and shNPM1 LNCaP cells cultured in RPMI 1640 10%FBS, were electrophoresed by SDS-PAGE. Transferred membranes were immunoblotted with indicated antibodies. Histograms show the band quantification reported to the beta-actin level. Blots are representative of three independent experiments with consistent results. Data are representative of at least three independent experiments and are expressed as the mean +/- SD. Image collected and cropped by CiteAb from the following publication (//dx.plos.org/10.1371/journal.pone.0096293), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/EGFR-Antibody-Western-Blot-NB100-596-img0016.jpg "<b>Biological Strategies Validation. </b>Western Blot: EGFR Antibody [NB100-596] - NPM1 knockdown decreases EGF expression. NPM1 controls activation of the EGF/EGFR pathway downstream effectors. Proteins, extracted from shScr and shNPM1 LNCaP cells cultured in RPMI 1640 10%FBS, were electrophoresed by SDS-PAGE. Transferred membranes were immunoblotted with indicated antibodies. Histograms show the band quantification reported to the beta-actin level. Blots are representative of three independent experiments with consistent results. Data are representative of at least three independent experiments and are expressed as the mean +/- SD. Image collected and cropped by CiteAb from the following publication (//dx.plos.org/10.1371/journal.pone.0096293), licensed under a CC-BY license.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: EGFR Antibody [NB100-596] - Section of human placenta. Antibody: Affinity purified rabbit anti-EGFR used at a dilution of 1:1,000 (1ug/ml). Detection: DAB.](http://images.novusbio.com/fullsize/EGFR-Antibody-Immunohistochemistry-Paraffin-NB100-596-img0013.jpg)
![<b>Biological Strategies Validation. </b>Western Blot: EGFR Antibody [NB100-596] - EGF R/ErbB1 Antibody [NB100-596] - Whole cell lysate (50 ug) from 293T and mouse NIH3T3 cells prepared using NETN lysis buffer. Antibody:Affinity purified rabbit anti-EGFR antibody used for WB at 0.04 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/EGFR-Antibody-Western-Blot-NB100-596-img0015.jpg)
![Western Blot: EGFR Antibody [NB100-596] - Detection of Human EGFR on HeLa whole cell lysate using NB100-596.](http://images.novusbio.com/fullsize/EGFR-Antibody-Western-Blot-NB100-596-img0005.jpg)
![Western Blot: EGFR Antibody [NB100-596] - Detection of Human EGFR by Western Blot. Samples: Whole cell lysate (5, 15 and 50 ug) from HeLa cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-EGFR antibody NB100-596 used for WB at 0.04 ug/ml. Detection: Chemiluminescence with an exposure time of 10 seconds.](http://images.novusbio.com/fullsize/EGFR-Antibody-Western-Blot-NB100-596-img0014.jpg)
![<b>Biological Strategies Validation. </b>Western Blot: EGFR Antibody [NB100-596] - NPM1 knockdown in prostate cancer cells reduces proliferation and migration capacities by inhibiting the EGF/EGFR pathway activity.(a) NPM1 down-regulation inhibits EGF induced ERK1/2 pathway activity. shScr and shNPM1 LNCaP cells were treated with 100 nM EGF and phosphorylation of the EGF/EGFR pathway effectors was analyzed using Western Blotting. Histograms show the band quantification reported to the beta-actin level. The blot is representative of three independent experiments with consistent results. Image collected and cropped by CiteAb from the following publication (//dx.plos.org/10.1371/journal.pone.0096293), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/EGFR-Antibody-Western-Blot-NB100-596-img0017.jpg)
![Western Blot: Cdk5 Antibody [NBP2-15843] - Wild-type (WT) and CDK5 knockout (KO) 293T cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with CDK5 antibody diluted at 1:500. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody](http://images.novusbio.com/fullsize/Cdk5-Antibody-Western-Blot-NBP2-15843-img0009.jpg "<b>Genetic Strategies Validation. </b>Western Blot: Cdk5 Antibody [NBP2-15843] - Wild-type (WT) and CDK5 knockout (KO) 293T cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with CDK5 antibody diluted at 1:500. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody")
![<b>Genetic Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Cdk5 Antibody [NBP2-15843] - Analysis of paraformaldehyde-fixed A549, using antibody at 1:200 dilution.](http://images.novusbio.com/fullsize/Cdk5-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-15843-img0004.jpg)
![Immunohistochemistry-Paraffin: Cdk5 Antibody [NBP2-15843] - Rat hind brain. CDK5 antibody [C2C3], C-term dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Cdk5-Antibody-Immunohistochemistry-Paraffin-NBP2-15843-img0005.jpg)
![Western Blot: Cdk5 Antibody [NBP2-15843] - Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with CDK5 antibody diluted at 1:500.](http://images.novusbio.com/fullsize/Cdk5-Antibody-Western-Blot-NBP2-15843-img0006.jpg)
![Western Blot: Cdk5 Antibody [NBP2-15843] - Sample (50 ug of whole cell lysate) A: mouse brain 12% SDS PAGE diluted at 1:1000](http://images.novusbio.com/fullsize/Cdk5-Antibody-Western-Blot-NBP2-15843-img0008.jpg)
![Immunohistochemistry-Paraffin: Cdk5 Antibody [NBP2-15843] - ES2 xenograft, using CDK5 antibody at 1:100 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Cdk5-Antibody-Immunohistochemistry-Paraffin-NBP2-15843-img0003.jpg)
![Western Blot: Aldolase A Antibody [NB600-915] - Analysis using Biotin conjugate of NB600-915. 300 ul aliquots of whole anti-aldolase antiserum used to precipitate varying amounts of purified aldolase & precipitates with controls; compared by SDS-PAGE & Western blot. 1. Purified aldolase 2. 300 ul antiserum with no antigen (negative control) 3. 300 ul antiserum with 100 ul aldolase (2.5 mg/ml) 4. 300 ul antiserum with 200 ul aldolase (2.5 mg/ml) For the precipitation, 300 ul of antiserum & an equal volume of aldolase antigen in PBS incubated 24 hrs at 4C, centrifuged for 6 mins at 13K RPM, washed once with PBS, centrifuged & dissolved in 60 ul 0.1 N NaOH. 90 ul of PBS was added, sample was divided in 2 portions, & an equal volume of reducing (+4% BME) or non-reducing 2X sample buffer added. The reduced samples were boiled for five mins, & all samples were run at 140 V for 45 mins on a 4-20% tris/glycine gradient gel. Gel was stained, destained & imaged.](http://images.novusbio.com/fullsize/Aldolase-A-Antibody-Western-Blot-NB600-915-img0010.jpg "Western Blot: Aldolase A Antibody [NB600-915] - Analysis using Biotin conjugate of NB600-915. 300 ul aliquots of whole anti-aldolase antiserum used to precipitate varying amounts of purified aldolase & precipitates with controls; compared by SDS-PAGE & Western blot. 1. Purified aldolase 2. 300 ul antiserum with no antigen (negative control) 3. 300 ul antiserum with 100 ul aldolase (2.5 mg/ml) 4. 300 ul antiserum with 200 ul aldolase (2.5 mg/ml) For the precipitation, 300 ul of antiserum & an equal volume of aldolase antigen in PBS incubated 24 hrs at 4C, centrifuged for 6 mins at 13K RPM, washed once with PBS, centrifuged & dissolved in 60 ul 0.1 N NaOH. 90 ul of PBS was added, sample was divided in 2 portions, & an equal volume of reducing (+4% BME) or non-reducing 2X sample buffer added. The reduced samples were boiled for five mins, & all samples were run at 140 V for 45 mins on a 4-20% tris/glycine gradient gel. Gel was stained, destained & imaged.")
![Western Blot: Aldolase A Antibody [NB600-915] - Figure. Immunoblotting. IgG purified antibody to rabbit muscle aldolase was used at a 1:1000 dilution to detect human aldolase by Western blot. A whole cell lysate prepared from human derived A293 cells was loaded on a 4-12% tris glycine gradient gel for SDS-PAGE. The gel was transferred to nitro-cellulose using standard techniques. Antibody reaction with the membrane occurred overnight at 4 degrees C in TTBS supplemented with 2% non-fat dry milk. Color was allowed to develop using SuperSignal West Pico Chemiluminescent Substrate (PIERCE). Other detection methods will yield similar results. This antibody clearly detects a band at ~41 kDa consistent with human aldolase.](http://images.novusbio.com/fullsize/Aldolase-A-Antibody-Western-Blot-NB600-915-img0003.jpg)
![Western Blot: Aldolase A Antibody [NB600-915] - IgG purified antibody to rabbit muscle aldolase was used at a 1:1000 dilution to detect human aldolase by Western blot. A whole cell lysate prepared from human derived A293 cells was loaded on a 4-12% tris glycine gradient gel for SDS-PAGE. The gel was transferred to nitro-cellulose using standard techniques. Antibody reaction with the membrane occurred overnight at 4 C in TTBS supplemented with 2% non-fat dry milk. Color was allowed to develop using SuperSignal West Pico Chemiluminescent Substrate (PIERCE).](http://images.novusbio.com/fullsize/Aldolase-A-Antibody-Western-Blot-NB600-915-img0009.jpg)
![Immunoprecipitation: Aldolase A Antibody [NB600-915] - Analysis using the Biotin conjugate of NB600-915. Detection of 300 ul of anti aldolase antiserum and an equal volume of varied amounts (diluted from a stock solution of ~2.5 ug/ml) of purified aldolase in PBS. Precipitation of aldolase was confirmed.](http://images.novusbio.com/fullsize/Aldolase-A-Antibody-Immunoprecipitation-NB600-915-img0005.jpg)
![Western Blot: Aldolase A Antibody [NB600-915] - Twenty one more markedly oxidized proteins identified in 6‐week‐old PLP‐tg66/66 mice in the spinal cord. All non‐mitochondrial oxidized proteins tested by Western blot in the spinal cord are normally expressed. Relative protein level expressed as a percentage of control and in reference to gamma ‐tubulin as a loading marker (n = 6/genotype). Image collected and cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/29027761/) licensed under a CC-BY license](http://images.novusbio.com/fullsize/nb600-915_goat-polyclonal-aldolase-a-antibody-2552023153959.jpg)
![Western Blot: PP2A alpha Antibody [NBP1-31266] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with PP2A alpha antibody. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/PP2A-alpha-Antibody-Western-Blot-NBP1-31266-img0013.jpg "<b>Genetic Strategies Validation. </b>Western Blot: PP2A alpha Antibody [NBP1-31266] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with PP2A alpha antibody. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: PPP2R4 Antibody [NBP1-31266] - Paraformaldehyde-fixed HeLa, using PP2A alpha antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with an alpha Tubulin antibody (Red) at 1:2000.](http://images.novusbio.com/fullsize/PPP2R4-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-31266-img0003.jpg)
![Immunohistochemistry-Paraffin: PP2A alpha Antibody [NBP1-31266] - A549 xenograft, using PPP2CA antibody at 1:100 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/PPP2R4-Antibody-Immunohistochemistry-Paraffin-NBP1-31266-img0004.jpg)
![Western Blot: PPP2R4 Antibody [NBP1-31266] - Sample (50 ug of whole cell lysate) A: mouse brain 10% SDS PAGE; antibody diluted at 1:10000.](http://images.novusbio.com/fullsize/PPP2R4-Antibody-Western-Blot-NBP1-31266-img0005.jpg)
![Western Blot: PPP2R4 Antibody [NBP1-31266] - Sample (30 ug of whole cell lysate) A: 293T B: Molt-4 10% SDS PAGE, antibody diluted at 1:1500.](http://images.novusbio.com/fullsize/PPP2R4-Antibody-Western-Blot-NBP1-31266-img0006.jpg)
![Immunoprecipitation: PP2A alpha Antibody [NBP1-31266] - Immunoprecipitation of PP2A alpha protein from 293T whole cell extracts using 5 ug of PP2A alpha antibody Western blot analysis was performed using PP2A alpha antibody. EasyBlot anti-Rabbit IgG was used as a secondary reagent.](http://images.novusbio.com/fullsize/PP2A-alpha-Antibody-Immunoprecipitation-NBP1-31266-img0011.jpg)
![Western Blot: PMS2 Antibody (163C1251) [NB100-56554] - Analysis of PMS2 using this antibody at 2 ug/ml against 10 ug of NIH 3T3 cell lysate.](http://images.novusbio.com/fullsize/PMS2-Antibody-163C1251-Western-Blot-NB100-56554-img0003.jpg "Western Blot: PMS2 Antibody (163C1251) [NB100-56554] - Analysis of PMS2 using this antibody at 2 ug/ml against 10 ug of NIH 3T3 cell lysate.")
![Immunohistochemistry-Paraffin: PMS2 Antibody (163C1251) [NB100-56554] - Analysis of formalin fixed paraffin-embedded (FFPE) human colon cancer using PMS2 antibody at 5 ug/ml on a Bond Rx autostainer (Leica Biosystems). The assay involved 20 minutes of heat induced antigen retrieval (HIER) using 10mM sodium citrate buffer (pH 6.0) and endogenous peroxidase quenching with peroxide block. The sections were incubated with primary antibody for 30 minutes and Bond Polymer Refine Detection (Leica Biosystems) with DAB was used for signal development followed by counterstaining with hematoxylin. Whole slide scanning and capturing of representative images was performed using Aperio AT2 (Leica Biosystems). Nuclear staining of PMS2 was observed. Staining was performed by Histowiz.](http://images.novusbio.com/fullsize/PMS2-Antibody-163C1251-Immunohistochemistry-Paraffin-NB100-56554-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: EGFR Antibody (GFR450) [NBP2-29440] - Confocal Immunofluorescent analysis of A431 cells using AF488-labeled Isotype Control Monoclonal Antibody (IgG2a) (Green). DAPI was used to stain the cell nuclei (blue). (Negative Control).](http://images.novusbio.com/fullsize/EGFR-Antibody-GFR450-Immunocytochemistry-Immunofluorescence-NBP2-29440-img0006.jpg "Immunocytochemistry/Immunofluorescence: EGFR Antibody (GFR450) [NBP2-29440] - Confocal Immunofluorescent analysis of A431 cells using AF488-labeled Isotype Control Monoclonal Antibody (IgG2a) (Green). DAPI was used to stain the cell nuclei (blue). (Negative Control).")
![Immunohistochemistry-Paraffin: EGFR Antibody (GFR450) [NBP2-29440] - Formalin-fixed, paraffin-embedded squamous cell carcinoma stained with EGFR Ab (GFR450).](http://images.novusbio.com/fullsize/EGFR-Antibody-GFR450-Immunohistochemistry-Paraffin-NBP2-29440-img0003.jpg)
![Flow Cytometry: EGFR Antibody (GFR450) [NBP2-29440] - Flow Cytometry of human EGFR on A431 cells. Black: cells alone; Grey: Isotype Control; Green: AF488-labeled EGFR antibody (GFR450).](http://images.novusbio.com/fullsize/EGFR-Antibody-GFR450-Flow-Cytometry-NBP2-29440-img0011.jpg)
![Immunocytochemistry/Immunofluorescence: EGFR Antibody (GFR450) [NBP2-29440] - Confocal Immunofluorescent analysis of A431 cells using AF488-labeled EGFR Monoclonal Antibody (GFR450) (Green). DAPI was used to stain the cell nuclei (blue).](http://images.novusbio.com/fullsize/EGFR-Antibody-GFR450-Immunocytochemistry-Immunofluorescence-NBP2-29440-img0005.jpg)
![Flow Cytometry: EGFR Antibody (GFR450) [NBP2-29440] - Flow Cytometry of human EGFR on A431 cells. Black: cells alone; Grey: Isotype Control; Green: AF488-labeled EGFR Antibody (GFR450).](http://images.novusbio.com/fullsize/EGFR-Antibody-GFR450-Flow-Cytometry-NBP2-29440-img0008.jpg)
![Protein Array: EGFR Antibody (GFR450) [NBP2-29440] - Analysis of Protein Array containing more than 19,000 full-length human proteins using EGFR Antibody (GFR450). 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/EGFR-Antibody-GFR450-Protein-Array-NBP2-29440-img0009.jpg)
![Western Blot: Prohibitin Antibody [NBP2-19944] - Sample (30 ug of whole cell lysate) A: IMR32 B: U87-MG 12% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/Prohibitin-Antibody-Western-Blot-NBP2-19944-img0001.jpg "Western Blot: Prohibitin Antibody [NBP2-19944] - Sample (30 ug of whole cell lysate) A: IMR32 B: U87-MG 12% SDS PAGE gel, diluted at 1:1000.")
![Immunohistochemistry-Paraffin: Prohibitin Antibody [NBP2-19944] - Immunohistochemical analysis of paraffin-embedded HBL435 xenograft, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/Prohibitin-Antibody-Immunohistochemistry-Paraffin-NBP2-19944-img0002.jpg)
![Immunohistochemistry-Paraffin: Prohibitin Antibody [NBP2-19944] - Paraffin-embedded mouse intestine. Prohibitin antibody dilution: 1:500.](http://images.novusbio.com/fullsize/Prohibitin-Antibody-Immunohistochemistry-Paraffin-NBP2-19944-img0003.jpg)
![Immunohistochemistry-Paraffin: RB1 Antibody [NBP2-20127] - Human colon carcinoma. Rb antibody dilution: 1:500. Antigen Retrieval: TrilogyTM (EDTA based) buffer, 15min](http://images.novusbio.com/fullsize/RB1-Antibody-Immunohistochemistry-Paraffin-NBP2-20127-img0005.jpg "Immunohistochemistry-Paraffin: RB1 Antibody [NBP2-20127] - Human colon carcinoma. Rb antibody dilution: 1:500. Antigen Retrieval: TrilogyTM (EDTA based) buffer, 15min")
![Immunoprecipitation: RB1 Antibody [NBP2-20127] - HeLa whole cell extract A. Control with 4 ug of preimmune Rabbit IgG B. Immunoprecipitation of retinoblastoma 1 protein by 4 ug Rb1 antibody 7.5 % SDS-PAGE The immunoprecipitated retinoblastoma 1 protein was detected by Rb1 antibody diluted at 1:500. [EasyBlot anti-rabbit IgG was used as a secondary reagent]](http://images.novusbio.com/fullsize/RB1-Antibody-Immunoprecipitation-NBP2-20127-img0004.jpg)
![Western Blot: HSP27 [p Ser78] Antibody [NBP2-24458] - Analysis of HSP27 (Ser78) in recombinant fusion protein containing 1) a phosphorylated serine at position 78 and 2) an unphosphorylated serine at position 78, using HSP27 phospho antibody at 0.01 ug/ml. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/Hsp27-[p-Ser78]-Antibody-Western-Blot-NBP2-24458-img0001.jpg "Western Blot: HSP27 [p Ser78] Antibody [NBP2-24458] - Analysis of HSP27 (Ser78) in recombinant fusion protein containing 1) a phosphorylated serine at position 78 and 2) an unphosphorylated serine at position 78, using HSP27 phospho antibody at 0.01 ug/ml. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")