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pe conjugated goat anti human igg  (SouthernBiotech)


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    Structured Review

    SouthernBiotech pe conjugated goat anti human igg
    Pe Conjugated Goat Anti Human Igg, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 95/100, based on 298 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/goat+anti+human+igg+fc/Goat+Anti-Human+IgG+Fc-PE/10__1038_slash_s41541___026___01598___3-321-9-13
    Average 95 stars, based on 298 article reviews
    pe conjugated goat anti human igg - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Binding Assay:

    Article Title: Heavy chain-only antibodies with a stabilized human VH in transgenic chickens for therapeutic antibody discovery
    Article Snippet: .. To calculate binding affinity, a capture kinetic method was used on a chip coupled with goat anti-human IgG Fc-specific polyclonal (Southern Biotech, 2047–01) capture reagent. .. Purified recombinant His-tagged PGRN (R&D systems) and NKp46 (prepared in-house) were used as monovalent analytes and prepared as a 3-fold dilution series with top concentrations of 300 nM or 1 μM.

    Article Title: Heavy chain-only antibodies with a stabilized human VH in transgenic chickens for therapeutic antibody discovery.
    Article Snippet: Binding kinetics, epitope mapping, and epitope binning experiments were performed by high-throughput surface plasmon resonance on Carterra’s LSA platform equipped with HC-30 M sensor chips. .. The method has been previously described in detail elsewhere.27 To calculate binding affinity, a capture kinetic method was used on a chip coupled with goat anti-human IgG Fc-specific polyclonal (Southern Biotech, 2047–01) capture reagent. .. Purified recombinant His-tagged PGRN (R&D systems) and NKp46 (prepared in-house) were used as monovalent analytes and prepared as a 3-fold dilution series with top concentrations of 300 nM or 1 μM.

    Generated:

    Article Title: Engineering a new tripartite split-ccGFP system from Corynactis californica for detecting protein–protein interactions
    Article Snippet: .. Capture surfaces were generated within the SFC via standard amine coupling of goat anti-human IgG Fc (SouthernBiotech #2047-01), creating a uniform “lawn” across the chip. .. The sensor surface was first activated by injecting a freshly prepared 1:1:1 (v/v/v) mixture of 0.4 M EDC (Carterra #9094), 0.1 M N-hydroxysulfosuccinimide (SNHS; ThermoFisher Scientific #24510), and 0.1 M MES (pH 5.5; Carterra #3625) for 7 min.

    Article Title: Engineering a new tripartite split-ccGFP system from Corynactis californica for detecting protein-protein interactions.
    Article Snippet: .. Capture surfaces were generated within the SFC via standard amine coupling of goat anti-human IgG Fc (SouthernBiotech #2047-01), creating a uniform “lawn” across the chip. .. The sensor surface was first activated by injecting a freshly prepared 1:1:1 (v/v/v) mixture of 0.4 M EDC (Carterra #9094), 0.1 M N-hydroxysulfosuccinimide (SNHS; ThermoFisher Scientific #24510), and 0.1 M MES (pH 5.5; Carterra #3625) for 7 min.



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    A . The binding of anti-gp41 7B2 to H9/N:L4-3 cells was demonstrated by indirect immunofluorescence and flow cytometry. The gray histogram indicates binding in the presence of <t>secondary</t> <t>FITC-conjugated</t> <t>goat</t> <t>anti-human</t> IgG only, the blue histogram demonstrates fluorescence of cells first incubated with 7B2 followed by FITC-conjugated secondary antibody. B. Comparative cytotoxicity of 7B2-dgA and 7B2-PNU. Cells were incubated with the indicated concentration of CIC and CD4-IgG2 (500 ng/mL) for 72 hr. MTS dye reduction was measured during the final 3 hr of culture. C. The kinetics of apoptosis induction by the CICs was measured by the binding of fluorescent annexin V to cells at different times following treatment with CIC.
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    A . The binding of anti-gp41 7B2 to H9/N:L4-3 cells was demonstrated by indirect immunofluorescence and flow cytometry. The gray histogram indicates binding in the presence of <t>secondary</t> <t>FITC-conjugated</t> <t>goat</t> <t>anti-human</t> IgG only, the blue histogram demonstrates fluorescence of cells first incubated with 7B2 followed by FITC-conjugated secondary antibody. B. Comparative cytotoxicity of 7B2-dgA and 7B2-PNU. Cells were incubated with the indicated concentration of CIC and CD4-IgG2 (500 ng/mL) for 72 hr. MTS dye reduction was measured during the final 3 hr of culture. C. The kinetics of apoptosis induction by the CICs was measured by the binding of fluorescent annexin V to cells at different times following treatment with CIC.
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    A . The binding of anti-gp41 7B2 to H9/N:L4-3 cells was demonstrated by indirect immunofluorescence and flow cytometry. The gray histogram indicates binding in the presence of <t>secondary</t> <t>FITC-conjugated</t> <t>goat</t> <t>anti-human</t> IgG only, the blue histogram demonstrates fluorescence of cells first incubated with 7B2 followed by FITC-conjugated secondary antibody. B. Comparative cytotoxicity of 7B2-dgA and 7B2-PNU. Cells were incubated with the indicated concentration of CIC and CD4-IgG2 (500 ng/mL) for 72 hr. MTS dye reduction was measured during the final 3 hr of culture. C. The kinetics of apoptosis induction by the CICs was measured by the binding of fluorescent annexin V to cells at different times following treatment with CIC.
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    Image Search Results


    A . The binding of anti-gp41 7B2 to H9/N:L4-3 cells was demonstrated by indirect immunofluorescence and flow cytometry. The gray histogram indicates binding in the presence of secondary FITC-conjugated goat anti-human IgG only, the blue histogram demonstrates fluorescence of cells first incubated with 7B2 followed by FITC-conjugated secondary antibody. B. Comparative cytotoxicity of 7B2-dgA and 7B2-PNU. Cells were incubated with the indicated concentration of CIC and CD4-IgG2 (500 ng/mL) for 72 hr. MTS dye reduction was measured during the final 3 hr of culture. C. The kinetics of apoptosis induction by the CICs was measured by the binding of fluorescent annexin V to cells at different times following treatment with CIC.

    Journal: bioRxiv

    Article Title: Anti-HIV Immunotoxin and Antibody-Drug Conjugate Display Both Common and Distinct Effects in Killing Target Cells

    doi: 10.64898/2026.04.07.717054

    Figure Lengend Snippet: A . The binding of anti-gp41 7B2 to H9/N:L4-3 cells was demonstrated by indirect immunofluorescence and flow cytometry. The gray histogram indicates binding in the presence of secondary FITC-conjugated goat anti-human IgG only, the blue histogram demonstrates fluorescence of cells first incubated with 7B2 followed by FITC-conjugated secondary antibody. B. Comparative cytotoxicity of 7B2-dgA and 7B2-PNU. Cells were incubated with the indicated concentration of CIC and CD4-IgG2 (500 ng/mL) for 72 hr. MTS dye reduction was measured during the final 3 hr of culture. C. The kinetics of apoptosis induction by the CICs was measured by the binding of fluorescent annexin V to cells at different times following treatment with CIC.

    Article Snippet: Cells were washed twice in PBS and incubated with 2 μg /mL of secondary FITC-conjugated goat anti-human IgG (Novus Biologicals, Centennial CO USA) for 1 hr at room temperature in the dark, then washed a final time with PBS and resuspended in 2% paraformaldehyde.

    Techniques: Binding Assay, Immunofluorescence, Flow Cytometry, Fluorescence, Incubation, Concentration Assay