Influenza A H1N1 PB2 Antibody - BSA Free
Novus Biologicals | Catalog # NBP2-42879
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Format
Product Specifications
Immunogen
Reactivity Notes
Clonality
Host
Isotype
Theoretical MW
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for Influenza A H1N1 PB2 Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence: Influenza A H1N1 PB2 Antibody [NBP2-42879]
Immunocytochemistry/Immunofluorescence: Influenza A H1N1 PB2 Antibody [NBP2-42879] - Analysis of A/WSN/33 infected Vero cells were fixed in 4% paraformaldehyde at RT for 20 min. Green: PB2 protein stained by Influenza A H1N1 PB2 antibody diluted at 1:500. Blue: DAPI staining. Yellow: WGA life stained at 37 degrees C,30 min.Western Blot: Influenza A H1N1 PB2 Antibody [NBP2-42879]
Western Blot: Influenza A H1N1 PB2 Antibody [NBP2-42879] - Analysis of 5 ug whole cell lysate. A: DF1 B: WSN virus infected DF1 10hr 7.5% SDS PAGE diluted at 1:5000.Western Blot: Influenza A H1N1 PB2 Antibody [NBP2-42879] -
Western Blot: Influenza A H1N1 PB2 Antibody [NBP2-42879] - 0.5 ug Influenza A viral lysate (0.5 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with Influenza A H1N1 PB2 antibody (NBP2-42879) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.Western Blot: Influenza A H1N1 PB2 Antibody [NBP2-42879] -
Non-infected (-) and infected (+) H1299 whole cell extracts (5 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Influenza A virus PB2 protein antibody (NBP2-42879) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
Species-dependent support of ANP32A or ANP32B for Influenza A viral replication.Vectors carrying 20 ng of ANP32A or ANP32B proteins, or empty vectors, were co-transfected into DKO cells, together with a minigenome reporter, a Renilla expression control, and influenza virus polymerases from either avian influenza H7N9ZJ13 (A) or H9N2ZJ12 (B); human influenza WSN (C); swine influenza H1N1NC08 (D); canine influenza H3N2GD11 (E); or equine influenza H3N8XJ07 (F). Luciferase activity was measured 24 h later. (Data are Firefly activity normalized to Renilla, Statistical differences between cells are labeled according to a one-way ANOVA followed by a Dunnett’s test; NS = not significant, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. The results represent at least three independent experiments.) ch, chicken; hu, human; sw, swine; eq, equine; ca, canine. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
ANP32A proteins from different species interact with different polymerase trimeric complexes.DKO cells were transfected with different ANP32A (0.6μg) and polymerase plasmids (0.6μg PA, 1μg PB1, and 1μg PB2) from avian influenza viruses H7N9ZJ13(A), H9N2ZJ12(B), human influenza virus polymerase WSN (C). The cells were lysed at 24 h post-transfection. Co-IP was performed using Anti-FLAG M2 Magnetic Beads, followed by Western blotting to detect the ANP32A and viral proteins by using specific antibodies: PA antibody (NBP2-42874, NOVUS), PB1 antibody (NBP2-42877, NOVUS), PB2 antibody (NBP2-42879, NOVUS), Anti-Flag antibody (F1804, SIGMA). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
Species-dependent support of ANP32A or ANP32B for Influenza A viral replication.Vectors carrying 20 ng of ANP32A or ANP32B proteins, or empty vectors, were co-transfected into DKO cells, together with a minigenome reporter, a Renilla expression control, and influenza virus polymerases from either avian influenza H7N9ZJ13 (A) or H9N2ZJ12 (B); human influenza WSN (C); swine influenza H1N1NC08 (D); canine influenza H3N2GD11 (E); or equine influenza H3N8XJ07 (F). Luciferase activity was measured 24 h later. (Data are Firefly activity normalized to Renilla, Statistical differences between cells are labeled according to a one-way ANOVA followed by a Dunnett’s test; NS = not significant, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. The results represent at least three independent experiments.) ch, chicken; hu, human; sw, swine; eq, equine; ca, canine. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
Species-dependent support of ANP32A or ANP32B for Influenza A viral replication.Vectors carrying 20 ng of ANP32A or ANP32B proteins, or empty vectors, were co-transfected into DKO cells, together with a minigenome reporter, a Renilla expression control, and influenza virus polymerases from either avian influenza H7N9ZJ13 (A) or H9N2ZJ12 (B); human influenza WSN (C); swine influenza H1N1NC08 (D); canine influenza H3N2GD11 (E); or equine influenza H3N8XJ07 (F). Luciferase activity was measured 24 h later. (Data are Firefly activity normalized to Renilla, Statistical differences between cells are labeled according to a one-way ANOVA followed by a Dunnett’s test; NS = not significant, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. The results represent at least three independent experiments.) ch, chicken; hu, human; sw, swine; eq, equine; ca, canine. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
ANP32A proteins from different species interact with different polymerase trimeric complexes.DKO cells were transfected with different ANP32A (0.6μg) and polymerase plasmids (0.6μg PA, 1μg PB1, and 1μg PB2) from avian influenza viruses H7N9ZJ13(A), H9N2ZJ12(B), human influenza virus polymerase WSN (C). The cells were lysed at 24 h post-transfection. Co-IP was performed using Anti-FLAG M2 Magnetic Beads, followed by Western blotting to detect the ANP32A and viral proteins by using specific antibodies: PA antibody (NBP2-42874, NOVUS), PB1 antibody (NBP2-42877, NOVUS), PB2 antibody (NBP2-42879, NOVUS), Anti-Flag antibody (F1804, SIGMA). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
Species-dependent support of ANP32A or ANP32B for Influenza A viral replication.Vectors carrying 20 ng of ANP32A or ANP32B proteins, or empty vectors, were co-transfected into DKO cells, together with a minigenome reporter, a Renilla expression control, and influenza virus polymerases from either avian influenza H7N9ZJ13 (A) or H9N2ZJ12 (B); human influenza WSN (C); swine influenza H1N1NC08 (D); canine influenza H3N2GD11 (E); or equine influenza H3N8XJ07 (F). Luciferase activity was measured 24 h later. (Data are Firefly activity normalized to Renilla, Statistical differences between cells are labeled according to a one-way ANOVA followed by a Dunnett’s test; NS = not significant, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. The results represent at least three independent experiments.) ch, chicken; hu, human; sw, swine; eq, equine; ca, canine. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
Species-dependent support of ANP32A or ANP32B for Influenza A viral replication.Vectors carrying 20 ng of ANP32A or ANP32B proteins, or empty vectors, were co-transfected into DKO cells, together with a minigenome reporter, a Renilla expression control, and influenza virus polymerases from either avian influenza H7N9ZJ13 (A) or H9N2ZJ12 (B); human influenza WSN (C); swine influenza H1N1NC08 (D); canine influenza H3N2GD11 (E); or equine influenza H3N8XJ07 (F). Luciferase activity was measured 24 h later. (Data are Firefly activity normalized to Renilla, Statistical differences between cells are labeled according to a one-way ANOVA followed by a Dunnett’s test; NS = not significant, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. The results represent at least three independent experiments.) ch, chicken; hu, human; sw, swine; eq, equine; ca, canine. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
ANP32A proteins from different species interact with different polymerase trimeric complexes.DKO cells were transfected with different ANP32A (0.6μg) and polymerase plasmids (0.6μg PA, 1μg PB1, and 1μg PB2) from avian influenza viruses H7N9ZJ13(A), H9N2ZJ12(B), human influenza virus polymerase WSN (C). The cells were lysed at 24 h post-transfection. Co-IP was performed using Anti-FLAG M2 Magnetic Beads, followed by Western blotting to detect the ANP32A and viral proteins by using specific antibodies: PA antibody (NBP2-42874, NOVUS), PB1 antibody (NBP2-42877, NOVUS), PB2 antibody (NBP2-42879, NOVUS), Anti-Flag antibody (F1804, SIGMA). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Influenza A H1N1 PB2 Antibody - BSA Free [NBP2-42879] -
Species-dependent support of ANP32A or ANP32B for Influenza A viral replication.Vectors carrying 20 ng of ANP32A or ANP32B proteins, or empty vectors, were co-transfected into DKO cells, together with a minigenome reporter, a Renilla expression control, and influenza virus polymerases from either avian influenza H7N9ZJ13 (A) or H9N2ZJ12 (B); human influenza WSN (C); swine influenza H1N1NC08 (D); canine influenza H3N2GD11 (E); or equine influenza H3N8XJ07 (F). Luciferase activity was measured 24 h later. (Data are Firefly activity normalized to Renilla, Statistical differences between cells are labeled according to a one-way ANOVA followed by a Dunnett’s test; NS = not significant, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. The results represent at least three independent experiments.) ch, chicken; hu, human; sw, swine; eq, equine; ca, canine. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/32084248), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for Influenza A H1N1 PB2 Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence
Immunoprecipitation
Western Blot
Formulation, Preparation, and Storage
Purification
Formulation
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Background: Influenza A H1N1 PB2
Alternate Names
Additional Influenza A H1N1 PB2 Products
Product Documents for Influenza A H1N1 PB2 Antibody - BSA Free
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Product Specific Notices for Influenza A H1N1 PB2 Antibody - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for Influenza A H1N1 PB2 Antibody - BSA Free
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunoprecipitation Protocol
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
FAQs for Influenza A H1N1 PB2 Antibody - BSA Free
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Q: i want to know the difference about these two produce (NBP2-42878 and NBP2-42879). only protein content?
A: The main difference is the immunogen used to make them. The N-terminal region of Influenza A virus PB2 was used for NBP2-42878, and the C-terminus was used for NBP2-42879. Therefore, NBP2-42878 recognizes the N-terminal region, and NBP2-42879 recognizes the C-terminal region.