polyclonal anti-vsv m (Boehringer Mannheim)
90
Structured Review
Boehringer Mannheim
polyclonal anti-vsv m
Polyclonal Anti Vsv M, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/polyclonal+anti-vsv+m/polyclonal+anti+vsv+m/pmc00104051-131-4-20
Average 90 stars, based on 1 article reviews
Polyclonal Anti Vsv M, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/polyclonal+anti-vsv+m/polyclonal+anti+vsv+m/pmc00104051-131-4-20
Average 90 stars, based on 1 article reviews
polyclonal anti-vsv m - by Bioz Stars,
2026-10
90/100 stars
Images
1) Product Images from "A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding"
Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding
Journal:
doi:
Figure Legend Snippet: VSV M budding assay. (A) Radiolabeled lysates from CV-1 cells receiving no DNA (mock, lane 2), T7VSVMWT DNA (MWT, lane 3), and T7VSVMY-A DNA (MY>A, lane 4) were immunoprecipitated with polyclonal antiserum against the M protein of VSV and fractioned by SDS-PAGE. The position of the M protein of VSV is indicated. MW, 14C-labeled protein standards. (B) Radiolabeled proteins released into the media covering cells transfected with no DNA (mock, lane 1), T7VSVMWT DNA (lane 2), and T7VSVMY-A DNA (lane 3) were immunoprecipitated with polyclonal antiserum against the M protein of VSV and fractionated by SDS-PAGE. The position of the M protein of VSV is indicated. (C) Radiolabeled lysates from CV-1 cells receiving no DNA (mock, lane 1), T7VSVMA4 DNA (lane 2), and T7VSVMWT DNA (lane 3) were immunoprecipitated with polyclonal antiserum raised against VSV virions (ATCC) and fractionated by SDS-PAGE. (D) Radiolabeled proteins released into the media covering cells transfected with no DNA (mock, lane 1), T7VSVMA4 (lane 2), and T7VSVMWT (lane 3) were immunoprecipitated with polyclonal antiserum raised against VSV virions (ATCC) and fractionated by SDS-PAGE.
Techniques Used: Immunoprecipitation, SDS Page, Labeling, Transfection
Figure Legend Snippet: Indirect immunofluorescence and confocal microscopy of transfected CV-1 cells. (A) CV-1 cells expressing wild-type VSV M protein at 8 h posttransfection. (B) CV-1 cells expressing the VSV M protein containing a tyrosine (Y) to alanine (A) mutation within the PY motif at 8 h posttransfection. (C) Untransfected CV-1 cells. Primary polyclonal antiserum (identical to that used in the experiment shown in Fig. Fig.7A7A and B) was directed against the M protein of VSV.
Techniques Used: Immunofluorescence, Confocal Microscopy, Transfection, Expressing, Mutagenesis
Related Articles
Affinity Purification:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Immunoprecipitation:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified SDS Page:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Labeling:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Transfection:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Immunofluorescence:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Confocal Microscopy:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Expressing:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified Mutagenesis:Article Title: A Proline-Rich Motif within the Matrix Protein of Vesicular Stomatitis Virus and Rabies Virus Interacts with WW Domains of Cellular Proteins: Implications for Viral Budding Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified |