| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48098 | |||
| Azide and BSA Free | NBP3-11399 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11608 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26196-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54380-100ug | |||
![Western Blot: MUPP1 Antibody [NBP1-49975] - Detection of Human MUPP1 by Western Blot and Immunoprecipitation. Samples: Whole cell lysate (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-MUPP1 antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate. MUPP1 was also immunoprecipitated by rabbit anti-MUPP1 antibody which recognizes an upstream epitope. For blotting immunoprecipitated MUPP1 was used. Detection: Chemiluminescence with exposure times of 3 minutes (A and B).](http://images.novusbio.com/fullsize/MUPP1-Antibody-Western-Blot-NBP1-49975-img0002.jpg "<b>Independent Antibodies Validation. </b>Western Blot: MUPP1 Antibody [NBP1-49975] - Detection of Human MUPP1 by Western Blot and Immunoprecipitation. Samples: Whole cell lysate (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-MUPP1 antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 3 mcg/mg lysate. MUPP1 was also immunoprecipitated by rabbit anti-MUPP1 antibody which recognizes an upstream epitope. For blotting immunoprecipitated MUPP1 was used. Detection: Chemiluminescence with exposure times of 3 minutes (A and B).")
![<b>Independent Antibodies Validation. </b>Western Blot: MUPP1 Antibody [NBP1-49975] - LDOC1 interacts with Ligand Of Numb-Protein X 1 (LNX1) to promote phospho-JAK2 (pJAK2) degradation through the ubiquitin–proteasome pathway. (A,B) LDOC1 enhances proteasomal degradation (A) & ubiquitination (B) of pJAK2 in basal & IL-6-stimulated A549-derived cell lines. A549-derived cell lines were starved overnight & pretreated with CHX (100 μg/mL), either alone or with proteasome inhibitor MG132 (20 uM) for 3 h before IL-6 (100 ng/mL) stimulation. The cells were lysed in an NP-40 lysis buffer containing MG132 (20 μg/mL) & ubiquitin aldehyde (20 μg/mL) to inhibit isopeptidase activities. (A) Western blotting was performed to examine the levels of indicated proteins. (B,C) The cell extracts were precleared with mouse or rabbit IgG (IgGm or IgGr, respectively) before being immunoprecipitated using antibodies against either pJAK2 (B,C) or against LDOC1 & LNX1 antibodies (C). The input & the Immunoprecipitation (IP) fractions were analyzed through immunoblotting (blot) using antibodies that recognized the indicated proteins. After being stripped, the membrane was reblotted with an anti-pJAK2 antibody (B). (D) Associations between LDOC1-LNX1 & LDOC1-pJAK2 in IL-6-treated A549 & A549-shCtrl-D10 cells. IL-6 stimulated cells were subjected to immunofluorescence assay (IFA) by using anti-LDOC1-DyLight594 (red), anti-LNX1-FITC (green), & anti-pJAK2-FITC (green), respectively. The 4′,6-diamidino-2-phenylindole (DAPI, blue) was used for nuclear counterstaining. Images were captured using a confocal microscope. IP or IFA performed with IgGm or IgGr were used as negative controls. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/30634502), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nbp1-49975_rabbit-polyclonal-mupp1-antibody-310202416175282.jpg)
![Immunohistochemistry-Paraffin: HLA A Antibody (SPM417) [NBP2-45317] - Human Tonsil stained with HLA A antibody.](http://images.novusbio.com/fullsize/HLA-A-Antibody-SPM417-Immunohistochemistry-Paraffin-NBP2-45317-img0001.jpg "Immunohistochemistry-Paraffin: HLA A Antibody (SPM417) [NBP2-45317] - Human Tonsil stained with HLA A antibody.")
![Immunocytochemistry/Immunofluorescence: CD2 Antibody (LFA2/600) [NBP2-44909] - Immunofluorescence staining of MOLT-4 cells using CD2 Antibody (LFA2/600) followed by goat anti-Mouse IgG conjugated to CF488 (green). Nuclei are stained with Red Dot.](http://images.novusbio.com/fullsize/CD2-Antibody-LFA2-600-Immunocytochemistry-Immunofluorescence-NBP2-44909-img0002.jpg "Immunocytochemistry/Immunofluorescence: CD2 Antibody (LFA2/600) [NBP2-44909] - Immunofluorescence staining of MOLT-4 cells using CD2 Antibody (LFA2/600) followed by goat anti-Mouse IgG conjugated to CF488 (green). Nuclei are stained with Red Dot.")
![Flow Cytometry: CD2 Antibody (LFA2/600) [NBP2-44909] - Flow Cytometric Analysis of MOLT-4 cells using CD2 Antibody (LFA2/600) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/CD2-Antibody-LFA2-600-Flow-Cytometry-NBP2-44909-img0001.jpg)
![Immunoprecipitation: SHIP Antibody (9G11) [NBP3-26196] - Immunoprecipitating SHIP in Raji whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26196 in Raji whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26196 (2ug) + Raji whole cell lysate(500ug). Lane 3: Raji whole cell lysate (10ug).](http://images.novusbio.com/fullsize/nbp3-26196_rabbit-ship-mab-9g11-26220241322154.jpg "Immunoprecipitation: SHIP Antibody (9G11) [NBP3-26196] - Immunoprecipitating SHIP in Raji whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26196 in Raji whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26196 (2ug) + Raji whole cell lysate(500ug). Lane 3: Raji whole cell lysate (10ug).")
![Immunohistochemistry: SHIP Antibody (9G11) [NBP3-26196] - Image of SHIP Antibody (9G11) diluted at 1:100 and staining in paraffin-embedded human tonsil tissue 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26196_rabbit-ship-mab-9g11-272202485633.jpg)
![Western Blot: SHIP Antibody (9G11) [NBP3-26196] - Positive Western Blot detected in: Raji whole cell lysate, K562 whole cell lysate. All lanes: SHIP Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 134, 110 kDa Observed band size: 145 kDa](http://images.novusbio.com/fullsize/nbp3-26196_rabbit-ship-mab-9g11-282202411472145.jpg)
![Functional: HLA Class I Antibody (mAb90) [DDX0250P-100] - mAb90 inhibits CD40-dependent B-cell proliferation. Tonsil B cells were cultured for 5 days on CD32-L cellsi n the presence of 1ug/ml anti-CD40 mAb with 1ug/ml of W6/32 or mAb90.](http://images.novusbio.com/fullsize/HLA-Class-I-Antibody-mAb90-Functional-Assay-DDX0250P-100-img0002.jpg "Functional: HLA Class I Antibody (mAb90) [DDX0250P-100] - mAb90 inhibits CD40-dependent B-cell proliferation. Tonsil B cells were cultured for 5 days on CD32-L cellsi n the presence of 1ug/ml anti-CD40 mAb with 1ug/ml of W6/32 or mAb90.")
![Functional: HLA Class I Antibody (mAb90) [DDX0250P-100] - mAb90 induces apoptosis of CD40-activated B cells. Cells were collected after 12 hours of treatment with the different mAbs and DNA from 2X104 cells was runon 2% agarose gel and stainedwith ethidiumbromide.](http://images.novusbio.com/fullsize/HLA-Class-I-Antibody-mAb90-Functional-Assay-DDX0250P-100-img0003.jpg)
![Western Blot: Aminopeptidase A/ENPEP Antibody [NBP1-32442] - Sample(30 ug whole cell lysate)A:Hep G2 7. 5% SDS PAGE, antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/Aminopeptidase-A-ENPEP-Antibody-Western-Blot-NBP1-32442-img0006.jpg "Western Blot: Aminopeptidase A/ENPEP Antibody [NBP1-32442] - Sample(30 ug whole cell lysate)A:Hep G2 7. 5% SDS PAGE, antibody diluted at 1:1000.")
![Immunohistochemistry-Paraffin: Aminopeptidase A/ENPEP Antibody [NBP1-32442] - Paraffin-embedded Kidney, using antibody 10 ug/ml.](http://images.novusbio.com/fullsize/Aminopeptidase-A-ENPEP-Antibody-Immunohistochemistry-Paraffin-NBP1-32442-img0005.jpg)
![Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (PSGL1/1601) [NBP2-53344] - Formalin-fixed, paraffin-embedded human Tonsil stained with PSGL-1/CD162 Antibody (PSGL1/1601).](http://images.novusbio.com/fullsize/PSGL-1-CD162-Antibody-PSGL1-1601-Immunohistochemistry-Paraffin-NBP2-53344-img0003.jpg "Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (PSGL1/1601) [NBP2-53344] - Formalin-fixed, paraffin-embedded human Tonsil stained with PSGL-1/CD162 Antibody (PSGL1/1601).")
![Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (PSGL1/1601) [NBP2-53344] - Formalin-fixed, paraffin-embedded human Spleen stained withCD162 Monoclonal Antibody (PSGL1/1601).](http://images.novusbio.com/fullsize/PSGL-1-CD162-Antibody-PSGL1-1601-Immunohistochemistry-Paraffin-NBP2-53344-img0001.jpg)
![Immunohistochemistry-Paraffin: PSGL-1/CD162 Antibody (PSGL1/1601) [NBP2-53344] - Formalin-fixed, paraffin-embedded human Tonsil stained withCD162 Monoclonal Antibody (PSGL1/1601).](http://images.novusbio.com/fullsize/PSGL-1-CD162-Antibody-PSGL1-1601-Immunohistochemistry-Paraffin-NBP2-53344-img0002.jpg)