Influenza A H1N1 PB2 Antibody - BSA Free

Novus Biologicals | Catalog # NBP2-42879

Novus Biologicals
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Key Product Details

Species Reactivity

Validated:

Virus

Cited:

Human, Porcine, Canine

Applications

Validated:

Western Blot, Immunocytochemistry/ Immunofluorescence, Immunoprecipitation

Cited:

Western Blot, Immunoprecipitation

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free
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Product Specifications

Immunogen

Recombinant protein encompassing a sequence within the C-terminus region of Influenza A virus PB2 (A/Puerto Rico/8/1934(H1N1)). The exact sequence is proprietary.

Reactivity Notes

Influenza A virus, Influenza A virus ( H1N1)

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Theoretical MW

86 kDa.
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]

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]

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.
Influenza A H1N1 PB2 Antibody

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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.
Influenza A H1N1 PB2 Antibody - BSA Free

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

Application
Recommended Usage

Immunocytochemistry/ Immunofluorescence

1:100-1:1000

Immunoprecipitation

Assay dependent

Western Blot

1:1000-1:10000

Formulation, Preparation, and Storage

Purification

Antigen Affinity-purified

Formulation

PBS, 1% BSA, 20% Glycerol

Format

BSA Free

Preservative

0.025% Proclin 300

Concentration

Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.

Background: Influenza A H1N1 PB2

Alternate Names

Influenza PB2

Additional Influenza A H1N1 PB2 Products

Product Documents for Influenza A H1N1 PB2 Antibody - BSA Free

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot or batch number in the search box below.

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.

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.

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