Review



b220-apc antibody  (Thermo Fisher)


Bioz Verified Symbol Thermo Fisher is a verified supplier
Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    Thermo Fisher b220-apc antibody
    B220 Apc Antibody, supplied by Thermo Fisher, 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/b220-apc antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    b220-apc antibody - by Bioz Stars, 2026-03
    90/100 stars

    Images



    Similar Products

    95
    Miltenyi Biotec anti b220
    Anti B220, supplied by Miltenyi Biotec, 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/anti b220/product/Miltenyi Biotec
    Average 95 stars, based on 1 article reviews
    anti b220 - by Bioz Stars, 2026-03
    95/100 stars
      Buy from Supplier

    90
    Thermo Fisher b220-apc antibody
    B220 Apc Antibody, supplied by Thermo Fisher, 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/b220-apc antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    b220-apc antibody - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Thermo Fisher cd45r[b220]-apc/efluor 780 antibody
    Cd45r[B220] Apc/Efluor 780 Antibody, supplied by Thermo Fisher, 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/cd45r[b220]-apc/efluor 780 antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    cd45r[b220]-apc/efluor 780 antibody - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    95
    Miltenyi Biotec b220 apc
    B220 Apc, supplied by Miltenyi Biotec, 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/b220 apc/product/Miltenyi Biotec
    Average 95 stars, based on 1 article reviews
    b220 apc - by Bioz Stars, 2026-03
    95/100 stars
      Buy from Supplier

    95
    Miltenyi Biotec rea755
    Rea755, supplied by Miltenyi Biotec, 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/rea755/product/Miltenyi Biotec
    Average 95 stars, based on 1 article reviews
    rea755 - by Bioz Stars, 2026-03
    95/100 stars
      Buy from Supplier

    95
    Miltenyi Biotec cd45r b220 apc vio770
    a Immunization scheme and sample collection schedule. Mice ( n = 5) were immunized intramuscularly at day 0 (prime) and 21(boost) with 1 µg of mRNA/animal. Blood samples were obtained at week 3 (prior to boost) and 6, and specific antibody levels were determined in serum. T-cell response was evaluated in splenocytes 3 weeks post-boost. b Reciprocal endpoint titers of antigen-specific IgG antibodies in serum samples determined by ELISA using RBD recombinant protein from wild-type variant. c Neutralization titers in serum samples were determined by neutralization assay using Spike-pseudotyped lentivirus and infection in HEK293T-ACE2-TMPRSS2 cells. NT50 titers refer to the dilution of a serum sample at which 50% of the pseudovirus infection is inhibited. d IFN-γ-secreting splenocytes quantification by ELISPOT after O.N. stimulation with SARS-CoV-2 Spike peptide pool. e IFN-γ quantification in supernatants of splenocytes after overnight stimulation with SARS-CoV-2 Spike peptide pool determined by ELISA. f T-lymphocyte CD4 and CD8 cell frequencies in spleen analyzed by flow cytometry. g Tfh and GC B cells analysis. Mice ( n = 5) were immunized intramuscularly with 5 µg of mRNA/animal. Inguinal lymph nodes were extracted on day 7. h Tfh <t>(CD45R</t> - , CD4 + , CD44hi, CXCR5 + , PD-1 + ) and GC B cell (CD19 + , CD95 + , GL7 + ) frequencies were determined by flow cytometry analysis. Graphs are represented as mean ± SD. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001 as determined by two-way ANOVA ( a ) and one-way ANOVA ( c – h ) with Tukey post-test.
    Cd45r B220 Apc Vio770, supplied by Miltenyi Biotec, 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/cd45r b220 apc vio770/product/Miltenyi Biotec
    Average 95 stars, based on 1 article reviews
    cd45r b220 apc vio770 - by Bioz Stars, 2026-03
    95/100 stars
      Buy from Supplier

    90
    Thermo Fisher b220-apc-efluor780 antibody
    a Immunization scheme and sample collection schedule. Mice ( n = 5) were immunized intramuscularly at day 0 (prime) and 21(boost) with 1 µg of mRNA/animal. Blood samples were obtained at week 3 (prior to boost) and 6, and specific antibody levels were determined in serum. T-cell response was evaluated in splenocytes 3 weeks post-boost. b Reciprocal endpoint titers of antigen-specific IgG antibodies in serum samples determined by ELISA using RBD recombinant protein from wild-type variant. c Neutralization titers in serum samples were determined by neutralization assay using Spike-pseudotyped lentivirus and infection in HEK293T-ACE2-TMPRSS2 cells. NT50 titers refer to the dilution of a serum sample at which 50% of the pseudovirus infection is inhibited. d IFN-γ-secreting splenocytes quantification by ELISPOT after O.N. stimulation with SARS-CoV-2 Spike peptide pool. e IFN-γ quantification in supernatants of splenocytes after overnight stimulation with SARS-CoV-2 Spike peptide pool determined by ELISA. f T-lymphocyte CD4 and CD8 cell frequencies in spleen analyzed by flow cytometry. g Tfh and GC B cells analysis. Mice ( n = 5) were immunized intramuscularly with 5 µg of mRNA/animal. Inguinal lymph nodes were extracted on day 7. h Tfh <t>(CD45R</t> - , CD4 + , CD44hi, CXCR5 + , PD-1 + ) and GC B cell (CD19 + , CD95 + , GL7 + ) frequencies were determined by flow cytometry analysis. Graphs are represented as mean ± SD. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001 as determined by two-way ANOVA ( a ) and one-way ANOVA ( c – h ) with Tukey post-test.
    B220 Apc Efluor780 Antibody, supplied by Thermo Fisher, 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/b220-apc-efluor780 antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    b220-apc-efluor780 antibody - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Thermo Fisher b220 ra3-6b2 apc-efluor780 antibody
    a Immunization scheme and sample collection schedule. Mice ( n = 5) were immunized intramuscularly at day 0 (prime) and 21(boost) with 1 µg of mRNA/animal. Blood samples were obtained at week 3 (prior to boost) and 6, and specific antibody levels were determined in serum. T-cell response was evaluated in splenocytes 3 weeks post-boost. b Reciprocal endpoint titers of antigen-specific IgG antibodies in serum samples determined by ELISA using RBD recombinant protein from wild-type variant. c Neutralization titers in serum samples were determined by neutralization assay using Spike-pseudotyped lentivirus and infection in HEK293T-ACE2-TMPRSS2 cells. NT50 titers refer to the dilution of a serum sample at which 50% of the pseudovirus infection is inhibited. d IFN-γ-secreting splenocytes quantification by ELISPOT after O.N. stimulation with SARS-CoV-2 Spike peptide pool. e IFN-γ quantification in supernatants of splenocytes after overnight stimulation with SARS-CoV-2 Spike peptide pool determined by ELISA. f T-lymphocyte CD4 and CD8 cell frequencies in spleen analyzed by flow cytometry. g Tfh and GC B cells analysis. Mice ( n = 5) were immunized intramuscularly with 5 µg of mRNA/animal. Inguinal lymph nodes were extracted on day 7. h Tfh <t>(CD45R</t> - , CD4 + , CD44hi, CXCR5 + , PD-1 + ) and GC B cell (CD19 + , CD95 + , GL7 + ) frequencies were determined by flow cytometry analysis. Graphs are represented as mean ± SD. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001 as determined by two-way ANOVA ( a ) and one-way ANOVA ( c – h ) with Tukey post-test.
    B220 Ra3 6b2 Apc Efluor780 Antibody, supplied by Thermo Fisher, 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/b220 ra3-6b2 apc-efluor780 antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    b220 ra3-6b2 apc-efluor780 antibody - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    Image Search Results


    a Immunization scheme and sample collection schedule. Mice ( n = 5) were immunized intramuscularly at day 0 (prime) and 21(boost) with 1 µg of mRNA/animal. Blood samples were obtained at week 3 (prior to boost) and 6, and specific antibody levels were determined in serum. T-cell response was evaluated in splenocytes 3 weeks post-boost. b Reciprocal endpoint titers of antigen-specific IgG antibodies in serum samples determined by ELISA using RBD recombinant protein from wild-type variant. c Neutralization titers in serum samples were determined by neutralization assay using Spike-pseudotyped lentivirus and infection in HEK293T-ACE2-TMPRSS2 cells. NT50 titers refer to the dilution of a serum sample at which 50% of the pseudovirus infection is inhibited. d IFN-γ-secreting splenocytes quantification by ELISPOT after O.N. stimulation with SARS-CoV-2 Spike peptide pool. e IFN-γ quantification in supernatants of splenocytes after overnight stimulation with SARS-CoV-2 Spike peptide pool determined by ELISA. f T-lymphocyte CD4 and CD8 cell frequencies in spleen analyzed by flow cytometry. g Tfh and GC B cells analysis. Mice ( n = 5) were immunized intramuscularly with 5 µg of mRNA/animal. Inguinal lymph nodes were extracted on day 7. h Tfh (CD45R - , CD4 + , CD44hi, CXCR5 + , PD-1 + ) and GC B cell (CD19 + , CD95 + , GL7 + ) frequencies were determined by flow cytometry analysis. Graphs are represented as mean ± SD. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001 as determined by two-way ANOVA ( a ) and one-way ANOVA ( c – h ) with Tukey post-test.

    Journal: NPJ Vaccines

    Article Title: Preserved efficacy of lyophilized SARS-CoV-2 mRNA vaccine incorporating novel ionizable lipids after one year at 25 °C

    doi: 10.1038/s41541-025-01201-1

    Figure Lengend Snippet: a Immunization scheme and sample collection schedule. Mice ( n = 5) were immunized intramuscularly at day 0 (prime) and 21(boost) with 1 µg of mRNA/animal. Blood samples were obtained at week 3 (prior to boost) and 6, and specific antibody levels were determined in serum. T-cell response was evaluated in splenocytes 3 weeks post-boost. b Reciprocal endpoint titers of antigen-specific IgG antibodies in serum samples determined by ELISA using RBD recombinant protein from wild-type variant. c Neutralization titers in serum samples were determined by neutralization assay using Spike-pseudotyped lentivirus and infection in HEK293T-ACE2-TMPRSS2 cells. NT50 titers refer to the dilution of a serum sample at which 50% of the pseudovirus infection is inhibited. d IFN-γ-secreting splenocytes quantification by ELISPOT after O.N. stimulation with SARS-CoV-2 Spike peptide pool. e IFN-γ quantification in supernatants of splenocytes after overnight stimulation with SARS-CoV-2 Spike peptide pool determined by ELISA. f T-lymphocyte CD4 and CD8 cell frequencies in spleen analyzed by flow cytometry. g Tfh and GC B cells analysis. Mice ( n = 5) were immunized intramuscularly with 5 µg of mRNA/animal. Inguinal lymph nodes were extracted on day 7. h Tfh (CD45R - , CD4 + , CD44hi, CXCR5 + , PD-1 + ) and GC B cell (CD19 + , CD95 + , GL7 + ) frequencies were determined by flow cytometry analysis. Graphs are represented as mean ± SD. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001 as determined by two-way ANOVA ( a ) and one-way ANOVA ( c – h ) with Tukey post-test.

    Article Snippet: Tfh cells were defined as CD45R - CD4 + , CD44 high , CXCR5 + , PD-1 + , and the following antibodies were used for surface staining: CD45R (B220)-APC-Vio770 (Miltenyi, 130-110-849), CD4-VioBright FITC (Miltenyi, 130-118-692), CD44-PerCP-Vio700 (Miltenyi, 130-128-625), CD185 (CXCR5)-APC (Miltenyi, 130-119-129), and CD279 (PD1)-PE (Miltenyi, 130-111-953).

    Techniques: Enzyme-linked Immunosorbent Assay, Recombinant, Variant Assay, Neutralization, Infection, Enzyme-linked Immunospot, Flow Cytometry