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![Western Blot: MAVS Antibody [NBP1-76768] - Rat brain tissue lysate with MAVS antibody at (A) 0.5, (B) 1 and (C) 2 ug/ml.](http://images.novusbio.com/fullsize/MAVS-Antibody-Western-Blot-NBP1-76768-img0001.jpg "Western Blot: MAVS Antibody [NBP1-76768] - Rat brain tissue lysate with MAVS antibody at (A) 0.5, (B) 1 and (C) 2 ug/ml.")
![Immunohistochemistry: MAVS Antibody - BSA Free [NBP1-76768] - Immunohistochemistry of MAVS in mouse brain tissue with MAVS antibody at 2.5 u/mL.](http://images.novusbio.com/fullsize/nbp1-76768_rabbit-polyclonal-mavs-antibody-27112024192889.jpg)
![Immunocytochemistry/ Immunofluorescence: MAVS Antibody - BSA Free [NBP1-76768] - Immunofluorescence of MAVS in Mouse Brain cells with MAVS antibody at 20 ug/mL.](http://images.novusbio.com/fullsize/nbp1-76768_rabbit-polyclonal-mavs-antibody-271120242022959.jpg)
![Immunohistochemistry-Paraffin: NLRP3/NALP3 Antibody [NB100-41104] - Human Tonsil shows focal and interstitial staining of the inflammatory elements close to the epithelia of the tonsil crypts.](http://images.novusbio.com/fullsize/NLRP3-NALP3-Antibody-Immunohistochemistry-Paraffin-NB100-41104-img0003.jpg "Immunohistochemistry-Paraffin: NLRP3/NALP3 Antibody [NB100-41104] - Human Tonsil shows focal and interstitial staining of the inflammatory elements close to the epithelia of the tonsil crypts.")
![ELISA: Human C4 binding protein A ELISA Kit (Colorimetric) [NBP2-60550] - Standard curve.](http://images.novusbio.com/fullsize/Human-C4-binding-protein-A-ELISA-Kit-Colorimetric-ELISA-NBP2-60550-img0001.jpg "ELISA: Human C4 binding protein A ELISA Kit (Colorimetric) [NBP2-60550] - Standard curve.")
![Immunohistochemistry-Paraffin: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of formalin-fixed, paraffin-embedded human liver](http://images.novusbio.com/fullsize/FPRL1-FPR2-Antibody-Immunohistochemistry-Paraffin-NBP3-14323-img0005.jpg "Immunohistochemistry-Paraffin: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of formalin-fixed, paraffin-embedded human liver")
![Immunohistochemistry-Paraffin: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of formalin-fixed, paraffin-embedded human spleen, neutrophils, after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/FPRL1-FPR2-Antibody-Immunohistochemistry-Paraffin-NBP3-14323-img0001.jpg)
![Immunohistochemistry-Paraffin: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of formalin-fixed, paraffin-embedded human lymph node, Hodgkins lymphoma, after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/FPRL1-FPR2-Antibody-Immunohistochemistry-Paraffin-NBP3-14323-img0002.jpg)
![Immunohistochemistry-Paraffin: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of formalin-fixed, paraffin-embedded human colon, neutrophils in crypt abscess, after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/FPRL1-FPR2-Antibody-Immunohistochemistry-Paraffin-NBP3-14323-img0003.jpg)
![Immunohistochemistry-Paraffin: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of formalin-fixed, paraffin-embedded human spleen](http://images.novusbio.com/fullsize/FPRL1-FPR2-Antibody-Immunohistochemistry-Paraffin-NBP3-14323-img0004.jpg)
![Immunohistochemistry: FPRL1/FPR2 Antibody [NBP3-14323] - Immunohistochemistry of breast, adenocarcinoma,](http://images.novusbio.com/fullsize/FPRL1-FPR2 Antibody-Immunohistochemistry-NBP3-14323-img0006.jpg)
![Western Blot: MAVS Antibody (PSH0-30) [NBP3-32569] - Western blot analysis of MAVS on different lysates with Rabbit anti-MAVS antibody (NBP3-32569) at 1/1,000 dilution. Lane 1: MCF7 cell lysate Lane 2: C2C12 cell lysate Lane 3: A431 cell lysate Lane 4: HeLa cell lysate Lane 5: A549 cell lysate Lane 6: Jurkat cell lysate Lane 7: THP-1 cell lysate Lane 8: NIH/3T3 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 56 kDa Observed band size: 75 kDa The molecular weight observed is consistent with that described in the literature (PMID: 16125763 and 30460894) Exposure time: 10S; 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 (NBP3-32569) 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 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32569_rabbit-mavs-mab-psh0-30-278202415212477.png "Western Blot: MAVS Antibody (PSH0-30) [NBP3-32569] - Western blot analysis of MAVS on different lysates with Rabbit anti-MAVS antibody (NBP3-32569) at 1/1,000 dilution. Lane 1: MCF7 cell lysate Lane 2: C2C12 cell lysate Lane 3: A431 cell lysate Lane 4: HeLa cell lysate Lane 5: A549 cell lysate Lane 6: Jurkat cell lysate Lane 7: THP-1 cell lysate Lane 8: NIH/3T3 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 56 kDa Observed band size: 75 kDa The molecular weight observed is consistent with that described in the literature (PMID: 16125763 and 30460894) Exposure time: 10S; 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 (NBP3-32569) 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 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: MAVS Antibody (PSH0-30) [NBP3-32569] - Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-MAVS antibody (NBP3-32569) 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 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32569) at 1/200 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/nbp3-32569_rabbit-mavs-mab-psh0-30-298202414115412.jpg)
![Immunocytochemistry/ Immunofluorescence: MAVS Antibody (PSH0-30) [NBP3-32569] - Immunocytochemistry analysis of A431 cells labeling MAVSwith Rabbit anti-MAVS antibody (NBP3-32569) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-MAVS antibody (NBP3-32569) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) was used as the secondary antibody at 1/1,000 dilution. 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 (Alexa Fluor® 647) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32569_rabbit-mavs-mab-psh0-30-29202410334019.png)
![Western Blot: MAVS Antibody (PSH01-65) [NBP3-32570] - Western blot analysis of MAVS on different lysates with Rabbit anti-MAVS antibody (NBP3-32570) at 1/1,000 dilution. Lane 1: MCF7 cell lysate Lane 2: A431 cell lysate Lane 3: A549 cell lysate Lane 4: Jurkat cell lysate Lane 5: THP-1 cell lysate Lane 6: HepG2 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 56.5 kDa Observed band size: 57/75 kDa Exposure time: 1 minute 46 seconds; 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 (NBP3-32570) 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/nbp3-32570_rabbit-mavs-mab-psh01-65-27820241631615.jpg "Western Blot: MAVS Antibody (PSH01-65) [NBP3-32570] - Western blot analysis of MAVS on different lysates with Rabbit anti-MAVS antibody (NBP3-32570) at 1/1,000 dilution. Lane 1: MCF7 cell lysate Lane 2: A431 cell lysate Lane 3: A549 cell lysate Lane 4: Jurkat cell lysate Lane 5: THP-1 cell lysate Lane 6: HepG2 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 56.5 kDa Observed band size: 57/75 kDa Exposure time: 1 minute 46 seconds; 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 (NBP3-32570) 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: MAVS Antibody (PSH01-65) [NBP3-32570] - Immunofluorescence analysis of paraffin-embedded human colon tissue labeling MAVS with Rabbit anti-MAVS antibody (NBP3-32570) 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 (NBP3-32570, 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/nbp3-32570_rabbit-mavs-mab-psh01-65-298202414262637.jpg)
![Immunohistochemistry: MAVS Antibody (PSH01-65) [NBP3-32570] - Immunohistochemical analysis of paraffin-embedded human kideny tissue with Rabbit anti-MAVS antibody (NBP3-32570) 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 (NBP3-32570) 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/nbp3-32570_rabbit-mavs-mab-psh01-65-29820241492697.jpg)
![Immunocytochemistry/ Immunofluorescence: MAVS Antibody (PSH01-65) [NBP3-32570] - Immunocytochemistry analysis of A431 cells labeling MAVS with Rabbit anti-MAVS antibody (NBP3-32570) 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-MAVS antibody (NBP3-32570) 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/nbp3-32570_rabbit-mavs-mab-psh01-65-2920241114838.jpg)
![Western Blot: CD43/Sialophorin Antibody (84-3C1) - Chimeric [NBP3-12075] - Daudi(A) cell lysate, K562(B) cell lysate and human bone marrow(C) tissue lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 84-3C1f (NBP3-12075) at 0.1 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-84-3C1-Chimeric-Western-Blot-NBP3-12075-img0001.jpg "Western Blot: CD43/Sialophorin Antibody (84-3C1) - Chimeric [NBP3-12075] - Daudi(A) cell lysate, K562(B) cell lysate and human bone marrow(C) tissue lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 84-3C1f (NBP3-12075) at 0.1 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.")
![Immunocytochemistry/Immunofluorescence: CD43/Sialophorin Antibody (84-3C1) - Chimeric [NBP3-12075] - Immunofluorescence analysis of paraformaldehyde fixed K562 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of 84-3C1 (NBP3-12075) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12075, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-84-3C1-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12075-img0002.jpg)
![Flow Cytometry: CD43/Sialophorin Antibody (84-3C1) - Chimeric - Azide and BSA Free [NBP3-12075] - K562 cells were fixed using 2% PFA and stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-12075 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-12075_rabbit-monoclonal-cd43-sialophorin-antibody-84-3c1-chimeric-74202522141237.png)
![Western Blot: CD43/Sialophorin Antibody [NBP2-32115] - Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) prepared using RIPA buffer from Jurkat cells. Antibodies: Affinity purified rabbit anti-CD43 antibody NBP2-32115 used for IP at 6 ug per reaction. CD43 was also immunoprecipitated by rabbit anti-CD43 antibody BL16255. For blotting immunoprecipitated CD43,NBP2-32115 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-Western-Blot-NBP2-32115-img0002.jpg "<b>Independent Antibodies Validation. </b>Western Blot: CD43/Sialophorin Antibody [NBP2-32115] - Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) prepared using RIPA buffer from Jurkat cells. Antibodies: Affinity purified rabbit anti-CD43 antibody NBP2-32115 used for IP at 6 ug per reaction. CD43 was also immunoprecipitated by rabbit anti-CD43 antibody BL16255. For blotting immunoprecipitated CD43,NBP2-32115 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.")
![<b>Independent Antibodies Validation. </b>Immunohistochemistry: CD43/Sialophorin Antibody [NBP2-32115] - Sample: FFPE section of human lung cancer infiltrating cells. Antibody: Affinity purified rabbit anti- CD43 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB. Counterstain: IHC Hematoxylin (blue).](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-Immunohistochemistry-NBP2-32115-img0005.jpg)
![Western Blot: CD43/Sialophorin Antibody [NBP2-32115] - Whole cell lysate (50 ug) prepared using RIPA buffer from HeLa, 293T, and Jurkat cells. Antibodies: Affinity purified rabbit anti-CD43 antibody NBP2-32115 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/CD43-Sialophorin-Antibody-Western-Blot-NBP2-32115-img0001.jpg)
![Immunohistochemistry-Paraffin: MyD88 Antibody [NBP2-19448] - Human lung papillory cancer, using MYD88 antibody at 1:500 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/MyD88-Antibody-Immunohistochemistry-Paraffin-NBP2-19448-img0002.jpg "Immunohistochemistry-Paraffin: MyD88 Antibody [NBP2-19448] - Human lung papillory cancer, using MYD88 antibody at 1:500 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.")
![Western Blot: MAVS Antibody [NBP2-49691] - Whole cell protein from MCF7 and A431 was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2 ug/ml anti-MAVS in 1% milk, and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.](http://images.novusbio.com/fullsize/MAVS-Antibody-Western-Blot-NBP2-49691-img0001.jpg "Western Blot: MAVS Antibody [NBP2-49691] - Whole cell protein from MCF7 and A431 was separated on a 7.5% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2 ug/ml anti-MAVS in 1% milk, and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.")
![Western Blot: IL-12 p70/IL-12A Antibody [NBP2-24627] - Analysis of IL-12A in recombinant IL-35 using IL-12A antibody at 4 ug/ml.](http://images.novusbio.com/fullsize/IL-12-p70-IL-12A-Antibody-Western-Blot-NBP2-24627-img0003.jpg "Western Blot: IL-12 p70/IL-12A Antibody [NBP2-24627] - Analysis of IL-12A in recombinant IL-35 using IL-12A antibody at 4 ug/ml.")