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polyclonal goat anti mouse igg alexa fluor 488  (SouthernBiotech)


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    Structured Review

    SouthernBiotech polyclonal goat anti mouse igg alexa fluor 488
    Polyclonal Goat Anti Mouse Igg Alexa Fluor 488, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 44 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alexa+fluor+488+polyclonal/bio_rxiv__64898__2026__03__30__715311-212-10-24?v=SouthernBiotech
    Average 93 stars, based on 44 article reviews
    polyclonal goat anti mouse igg alexa fluor 488 - by Bioz Stars, 2026-08
    93/100 stars

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    Bioss hpv16 e7 alexafluor 488
    ( A ) Schematics of three SNA designs presenting the HLA-A2–restricted <t>HPV16</t> E7 11-19 peptide: E-SNA (peptide encapsulated in the liposomal core), N-HSNA (peptide displayed on the SNA surface via N-terminal DNA conjugation), and C-HSNA (peptide displayed via C-terminal conjugation). DNA-peptide conjugates were synthesized using a SPDP linker and a site-specific additional cysteine residue at either the N or C terminus of the peptide. ( B ) Zeta potential measurements comparing SNA formulations with liposomes. ( C ) Number mean size distribution of SNAs and liposomes measured by DLS. Data represent mean ± SD ( n = 3). ( D ) Cryo–electron microscopy (cryo-EM) images of E-SNA, N-HSNA, and C-HSNA. Particle size quantification was performed on at least 50 particles per group. Scale bars, 50 nm.
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    Image Search Results


    ( A ) Schematics of three SNA designs presenting the HLA-A2–restricted HPV16 E7 11-19 peptide: E-SNA (peptide encapsulated in the liposomal core), N-HSNA (peptide displayed on the SNA surface via N-terminal DNA conjugation), and C-HSNA (peptide displayed via C-terminal conjugation). DNA-peptide conjugates were synthesized using a SPDP linker and a site-specific additional cysteine residue at either the N or C terminus of the peptide. ( B ) Zeta potential measurements comparing SNA formulations with liposomes. ( C ) Number mean size distribution of SNAs and liposomes measured by DLS. Data represent mean ± SD ( n = 3). ( D ) Cryo–electron microscopy (cryo-EM) images of E-SNA, N-HSNA, and C-HSNA. Particle size quantification was performed on at least 50 particles per group. Scale bars, 50 nm.

    Journal: Science Advances

    Article Title: E7 11-19 placement and orientation dictate CD8 + T cell response in structurally defined spherical nucleic acid vaccines

    doi: 10.1126/sciadv.aec3876

    Figure Lengend Snippet: ( A ) Schematics of three SNA designs presenting the HLA-A2–restricted HPV16 E7 11-19 peptide: E-SNA (peptide encapsulated in the liposomal core), N-HSNA (peptide displayed on the SNA surface via N-terminal DNA conjugation), and C-HSNA (peptide displayed via C-terminal conjugation). DNA-peptide conjugates were synthesized using a SPDP linker and a site-specific additional cysteine residue at either the N or C terminus of the peptide. ( B ) Zeta potential measurements comparing SNA formulations with liposomes. ( C ) Number mean size distribution of SNAs and liposomes measured by DLS. Data represent mean ± SD ( n = 3). ( D ) Cryo–electron microscopy (cryo-EM) images of E-SNA, N-HSNA, and C-HSNA. Particle size quantification was performed on at least 50 particles per group. Scale bars, 50 nm.

    Article Snippet: The directly conjugated antibodies used for PDOTS staining were CD45-AlexaFluor-647 (BioLegend, HI30), EGFR-AbBy Fluor-594 (BioLegend, AY13), and HPV16 E7-AlexaFluor-488 (Bioss).

    Techniques: Conjugation Assay, Synthesized, Residue, Zeta Potential Analyzer, Liposomes, Cryo-Electron Microscopy, Cryo-EM Sample Prep