primary antibodies vsv-m Search Results


polyclonal anti-vsv m  (Boehringer Mannheim)
90
Boehringer Mannheim polyclonal anti-vsv m
<t>VSV</t> <t>M</t> 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 <t>polyclonal</t> 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.
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/result/polyclonal anti-vsv m/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
polyclonal anti-vsv m - by Bioz Stars, 2026-05
90/100 stars
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primary antibodies  (Santa Cruz Biotechnology)
95
Santa Cruz Biotechnology primary antibodies
<t>VSV</t> <t>M</t> 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 <t>polyclonal</t> 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.
Primary Antibodies, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies/product/Santa Cruz Biotechnology
Average 95 stars, based on 1 article reviews
primary antibodies - by Bioz Stars, 2026-05
95/100 stars
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anti-vsv-m monoclonal antibody, clone 34i23  (Creative BioMart)
N/A
This monoclonal antibody reacts with VSV-M protein.-20°C (avoid repeated freeze / thaw cycles)http://www.creative-diagnostics.com/VSV-M-antibody-238781-144.htm
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Image Search Results


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.

Journal:

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

doi:

Figure Lengend 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.

Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified goat anti-rabbit antibody conjugated to fluorescein isothiocyanate (Boehringer Mannheim Corporation).

Techniques: Immunoprecipitation, SDS Page, Labeling, Transfection

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.

Journal:

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

doi:

Figure Lengend 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.

Article Snippet: The primary antibody was polyclonal anti-VSV M, while the secondary antibody was affinity-purified goat anti-rabbit antibody conjugated to fluorescein isothiocyanate (Boehringer Mannheim Corporation).

Techniques: Immunofluorescence, Confocal Microscopy, Transfection, Expressing, Mutagenesis