Recombinant Mouse Anti-IAV M2 protein Antibody (mAb 65) (CAT#: PABL-226)

Recombinant Mouse Antibody (mAb 65) is capable of binding to IAV M2 protein, expressed in Chinese Hamster Ovary cells (CHO).


Specific Inquiry
  • Size:
  • Conjugation:
  • Endotoxin:
  • Purity:
  • Fc Engineering:
  • Published Data
  • Tested Data
  • Datasheet
  • MSDS
  • COA

Figure 1 Reactivity of MAb 65 and 14C2 with M2 was analyzed by Western blotting of lysates of HEK-293T cells transfected with M2-Flag expressionconstructs carrying M2e-Ala mutants. Anti-Flag detection was used to normalize the amount of M2 in the cell lysates that were loaded. NC, negative control.

Figure 1 Reactivity of MAb 65 and 14C2 with M2 was analyzed by Western blotting of lysates of HEK-293T cells transfected with M2-Flag expressionconstructs carrying M2e-Ala mutants. Anti-Flag detection was used to normalize the amount of M2 in the cell lysates that were loaded. NC, negative control.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 2 Confocal images of immunofluorescence staining of MDCK cells infected with in-fluenza virus.

Figure 2 Confocal images of immunofluorescence staining of MDCK cells infected with in-fluenza virus.

M2 staining is shown in red fluorescence and was revealed usingMAb 65 or MAb 148 (a TCN-031-like antibody that binds to the N terminus ofM2). Goat polyclonal antibody against influenza virus ribonucleoprotein (BEIResources, no. NR-3133) was used to stain viral RNPs (green). Cell nuclei were identified by DAPI staining (blue).

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 3 MAb 65 does not affect influenza A virus plaque size.

Figure 3 MAb 65 does not affect influenza A virus plaque size.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 4 Properties of binding of MAb 65 to M2e peptide and M2-expressing cells.

Figure 4 Properties of binding of MAb 65 to M2e peptide and M2-expressing cells.

Binding of MAb 65 and MAb 148 to different M2e peptides. ELISA plateswere coated with wild-type (WT), M2eW15G, or M2eP10L M2e peptides at 20 ng/ml or 200 ng/ml.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 5 Cellular ELISA using HEK-293T cells that had been transfected with wild-type, M2Trp15Ala, or M2Pro10Ala M2-Flag expression vectors.

Figure 5 Cellular ELISA using HEK-293T cells that had been transfected with wild-type, M2Trp15Ala, or M2Pro10Ala M2-Flag expression vectors.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 6  Western blot analysis of cell lysates prepared 24 h after transfection to evaluateexpression of NP, M2 (revealed by staining with MAb 148 and MAb 65) and M1, as indicated. WT, wild type; NC, negative control (i.e., transfected with only pCAXL-PA, pCAXL-PB1, pCAXL-PB2, and pCAXL-NP); ST, mutant with stop codons introduced after M2-Asp24; NT, nontransfected.

Figure 6 Western blot analysis of cell lysates prepared 24 h after transfection to evaluateexpression of NP, M2 (revealed by staining with MAb 148 and MAb 65) and M1, as indicated. WT, wild type; NC, negative control (i.e., transfected with only pCAXL-PA, pCAXL-PB1, pCAXL-PB2, and pCAXL-NP); ST, mutant with stop codons introduced after M2-Asp24; NT, nontransfected.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 7 Plaque assay toquantify rescued PR/8 viruses with introduced M1/M2Trp15 mutations.

Figure 7 Plaque assay toquantify rescued PR/8 viruses with introduced M1/M2Trp15 mutations.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.

Figure 8 Hemagglutinating activity in the supernatants of transfected HEK293T-MDCKcocultures. The supernatant and serial 3-fold dilutions were assayed for hemagglutination of chicken red blood cells on day 2 or 5 after transfection with theeight-plasmid system used for generating PR/8 virus.

Figure 8 Hemagglutinating activity in the supernatants of transfected HEK293T-MDCKcocultures. The supernatant and serial 3-fold dilutions were assayed for hemagglutination of chicken red blood cells on day 2 or 5 after transfection with theeight-plasmid system used for generating PR/8 virus.

Cho, K. J., Schepens, B., Seok, J. H., Kim, S., Roose, K., Lee, J. H.,... & Fiers, W. (2015). Structure of the extracellular domain of matrix protein 2 of influenza A virus in complex with a protective monoclonal antibody. Journal of virology, 89(7), 3700-3711.


Specifications

  • Immunogen
  • Influenza a virus matrix protein 2
  • Host Species
  • Mouse
  • Derivation
  • Mouse
  • Type
  • IgG
  • Specificity
  • Tested positive against native IAV M2 protein
  • Species Reactivity
  • IAV
  • Clone
  • mAb 65
  • Applications
  • IF, FuncS, ELISA, WB, Plaque assay, Hemagglutinating activity

Product Property

  • Purity
  • >95% by SDS-PAGE and HPLC analysis
  • Storage
  • Store the antibody (in aliquots) at -20°C. Avoid repeated freezing and thawing of samples.

Applications

  • Application Notes
  • The antibody was validated for ELISA, Immunofluorescence, Western Blot, Plaque assay, Function Assay and Hemagglutinating activity. For details, refer to Published Data.

Target

  • Alternative Names
  • M2 protein; matrix protein 2; M2e

Product Notes

This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:

• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production

See more details about Hi-Affi™ recombinant antibody benefits.

Downloads

Download resources about recombinant antibody development and antibody engineering to boost your research.

See other products for "Clone mAb 65"

See other products for "M2 protein"

scFv Fragment Antibody

Fab Fragment Antibody

Recombinant Antibody

MHC Tetramer for Other Applications

Customer Reviews and Q&As

Submit a review or a question
There are currently no Customer reviews or questions for PABL-226. Click the button above to contact us or submit your feedback about this product.
View the frequently asked questions answered by Creative Biolabs Support.

For Research Use Only. Not For Clinical Use.

For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

Send Inquiry

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

© 2024 Creative Biolabs.
  • 0
  • 0
Cart

    Go to compare