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iv) pe anti-mouse igm (rat igg2a; miltenyi 130-095-908  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec iv) pe anti-mouse igm (rat igg2a; miltenyi 130-095-908
    Iv) Pe Anti Mouse Igm (Rat Igg2a; Miltenyi 130 095 908, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 50 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/igg2a+pe/IgM+Antibody%2C+anti-mouse/pm42455073-74-69-75
    Average 95 stars, based on 50 article reviews
    iv) pe anti-mouse igm (rat igg2a; miltenyi 130-095-908 - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Bioprocessing:

    Article Title: Purification of Stem Cells from Oral Pyogenic Granuloma Tissue
    Article Snippet: The isolated cells were incubated for 10-30 minutes in a dark environment with the following anti-human antibodies: CD90- fluorescein isothiocianate (FITC), CD 34- phycoeritrin (PE), CD 45- Peridinin chlorophyll protein (PerCP), CD 271-FITC (MiltenyiBiotec), CD106-PE, CD 44-FITC, CD73-PE, CD14-FITC (BD Biosciences), and CD105-PerCP (AbDSerotec, Kidlington, Oxford, England). .. Isotype-matched irrelevant monoclonal antibodies such as Mouse IgG1-PE, IgG2a-FITC (AbDSerotec, Kidlington, Oxford, England), IgG2a-PerCP, IgG2b-FITC and IgG2a-PE (Miltenyi Biotec) were used to omit the effect of non-specific cells staining. .. Flow cytometry analysis was done in a FACS Calibur device (BD Biosciences) by using the cell quest as data acquisition software.

    Staining:

    Article Title: Purification of Stem Cells from Oral Pyogenic Granuloma Tissue
    Article Snippet: The isolated cells were incubated for 10-30 minutes in a dark environment with the following anti-human antibodies: CD90- fluorescein isothiocianate (FITC), CD 34- phycoeritrin (PE), CD 45- Peridinin chlorophyll protein (PerCP), CD 271-FITC (MiltenyiBiotec), CD106-PE, CD 44-FITC, CD73-PE, CD14-FITC (BD Biosciences), and CD105-PerCP (AbDSerotec, Kidlington, Oxford, England). .. Isotype-matched irrelevant monoclonal antibodies such as Mouse IgG1-PE, IgG2a-FITC (AbDSerotec, Kidlington, Oxford, England), IgG2a-PerCP, IgG2b-FITC and IgG2a-PE (Miltenyi Biotec) were used to omit the effect of non-specific cells staining. .. Flow cytometry analysis was done in a FACS Calibur device (BD Biosciences) by using the cell quest as data acquisition software.

    Labeling:

    Article Title: Recovery and assessment of leukocytes from LR Express filters
    Article Snippet: .. The fluorescently labeled antibodies used for this study included IgG1 FITC, IgG2a PE, IgG1 PerCP-Cy5.5, IgG2a APC, CD14 PE, CD4 APC, CD3 FITC, HLA-DR FITC, CD4 PerCP-Cy5.5, and CD8 (BD Biosciences) and CD83 APC and CD86 FITC (Miltenyi). .. In some experiments, cells were labeled with carboxyfluorescein diacetate succinimidyl ester (CFSE; Invitrogen) according to the manufacturer’s protocol.

    Article Title: Recovery and assessment of leukocytes from LR Express filters.
    Article Snippet: .. The fluorescently labeled antibodies used for this study included IgG1 FITC, IgG2a PE, IgG1 PerCP-Cy5.5, IgG2a APC, CD14 PE, CD4 APC, CD3 FITC, HLA-DR FITC, CD4 PerCP-Cy5.5, and CD8 (BD Biosciences) and CD83 APC and CD86 FITC (Miltenyi). .. In some experiments, cells were labeled with carboxyfluorescein diacetate succinimidyl ester (CFSE; Invitrogen) according to the manufacturer's protocol.

    Flow Cytometry:

    Article Title: Spheroid Coculture of Hematopoietic Stem/Progenitor Cells and Monolayer Expanded Mesenchymal Stem/Stromal Cells in Polydimethylsiloxane Microwells Modestly Improves In Vitro Hematopoietic Stem/Progenitor Cell Expansion
    Article Snippet: .. Flow cytometry analysis of trypsin-dissociated cultures was performed using antibodies for CD45-FITC, CD34-APC, and CD38-PE and corresponding isotype controls IgG2a-FITC, IgG2a-APC, and IgG2a-PE, all from Miltenyi and used as per the manufacturer's instructions. .. Cells were enumerated using fluorospheres (Beckman Coulter).



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    SouthernBiotech goat anti mouse igg2a
    Antibody titers against M. haemolytica and IgG subclass analysis ( n = 10). ( A ) The immunization procedure for titer evaluation. ( B ) BALB/c mice were immunized with rND-white oil, rND-propolis, and rND-Astragalus Polysaccharide Adjuvant, and commercial vaccines, and the serum IgG titers against M. haemolytica were determined. PBS group were used as a control. IgG titer measurements began seven days after the first injection. One-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. ( C ) <t>IgG2a</t> /IgG1 at OD 450 nm. ( D ) The serum IgG subtype titers against M. haemolytica after the third immunization (IgG1, IgG2a, IgG2b, and IgG3). Two-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. **** P < 0.0001, * * P < 0.001, ** P < 0.01, * P < 0.05, ns > 0.05
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    Image Search Results


    Antibody titers against M. haemolytica and IgG subclass analysis ( n = 10). ( A ) The immunization procedure for titer evaluation. ( B ) BALB/c mice were immunized with rND-white oil, rND-propolis, and rND-Astragalus Polysaccharide Adjuvant, and commercial vaccines, and the serum IgG titers against M. haemolytica were determined. PBS group were used as a control. IgG titer measurements began seven days after the first injection. One-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. ( C ) IgG2a /IgG1 at OD 450 nm. ( D ) The serum IgG subtype titers against M. haemolytica after the third immunization (IgG1, IgG2a, IgG2b, and IgG3). Two-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. **** P < 0.0001, * * P < 0.001, ** P < 0.01, * P < 0.05, ns > 0.05

    Journal: BMC Veterinary Research

    Article Title: Antigenicity analysis of the recombinant fusion proteins NlpI of Mannheimia haemolytica and DsbA of Pasteurella multocida

    doi: 10.1186/s12917-025-05233-6

    Figure Lengend Snippet: Antibody titers against M. haemolytica and IgG subclass analysis ( n = 10). ( A ) The immunization procedure for titer evaluation. ( B ) BALB/c mice were immunized with rND-white oil, rND-propolis, and rND-Astragalus Polysaccharide Adjuvant, and commercial vaccines, and the serum IgG titers against M. haemolytica were determined. PBS group were used as a control. IgG titer measurements began seven days after the first injection. One-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. ( C ) IgG2a /IgG1 at OD 450 nm. ( D ) The serum IgG subtype titers against M. haemolytica after the third immunization (IgG1, IgG2a, IgG2b, and IgG3). Two-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. **** P < 0.0001, * * P < 0.001, ** P < 0.01, * P < 0.05, ns > 0.05

    Article Snippet: ProteinIso Ni-NTA Resin was purchased from Beijing All-Golden Biota; Ampicillin(Amp+, 100 mg/ml solution), IPTG(Isopropyl β-D- Thiogalactopyranoside), ELISA coating solution, 5% BSA blocking solution, ELISA termination solution, two-component TMB chromogenic solution, 10× PBST, and 20× TBST were purchased from Beijing Soleibao Technology Co., Ltd.; hRP AffiniPure Goat Anti-Mouse IgG (H + L) from EarthOx; Goat Anti-Mouse IgG1, Human ads-HRP, Goat Anti-Mouse IgG2a, Human ads-HRP, Goat Anti-Mouse IgG2b-HRP and Goat Anti-Mouse IgG3-HRP were purchased from Southern Biotech; the LB medium was purchased from hopebiol Co., Ltd.

    Techniques: Adjuvant, Vaccines, Control, Injection, Comparison

    Antibody titers against P. multocida and IgG subclass analysis ( n = 10). ( A ) BALB/c mice were immunized with rND-white oil, rND-propolis and rND-astragalus polysaccharide adjuvants, and the serum IgG titers against P.multocida in were determined. PBS group were used as a control. IgG titer measurement began seven days after the first injection. One-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. ( B ) IgG2a/IgG1 at OD 450 nm. ( C ) The serum IgG subtype titers against P. multocida after the third immunization (IgG1, IgG2a, IgG2b, and IgG3). Two-way ANOVA with Dunnett ‘s multiple comparison test was used to compare the groups. **** P < 0.0001; *** P < 0.001; ** P < 0.01; * P < 0.05; ns, P > 0.05

    Journal: BMC Veterinary Research

    Article Title: Antigenicity analysis of the recombinant fusion proteins NlpI of Mannheimia haemolytica and DsbA of Pasteurella multocida

    doi: 10.1186/s12917-025-05233-6

    Figure Lengend Snippet: Antibody titers against P. multocida and IgG subclass analysis ( n = 10). ( A ) BALB/c mice were immunized with rND-white oil, rND-propolis and rND-astragalus polysaccharide adjuvants, and the serum IgG titers against P.multocida in were determined. PBS group were used as a control. IgG titer measurement began seven days after the first injection. One-way ANOVA with Dunnett’s multiple comparison test was used to compare the groups. ( B ) IgG2a/IgG1 at OD 450 nm. ( C ) The serum IgG subtype titers against P. multocida after the third immunization (IgG1, IgG2a, IgG2b, and IgG3). Two-way ANOVA with Dunnett ‘s multiple comparison test was used to compare the groups. **** P < 0.0001; *** P < 0.001; ** P < 0.01; * P < 0.05; ns, P > 0.05

    Article Snippet: ProteinIso Ni-NTA Resin was purchased from Beijing All-Golden Biota; Ampicillin(Amp+, 100 mg/ml solution), IPTG(Isopropyl β-D- Thiogalactopyranoside), ELISA coating solution, 5% BSA blocking solution, ELISA termination solution, two-component TMB chromogenic solution, 10× PBST, and 20× TBST were purchased from Beijing Soleibao Technology Co., Ltd.; hRP AffiniPure Goat Anti-Mouse IgG (H + L) from EarthOx; Goat Anti-Mouse IgG1, Human ads-HRP, Goat Anti-Mouse IgG2a, Human ads-HRP, Goat Anti-Mouse IgG2b-HRP and Goat Anti-Mouse IgG3-HRP were purchased from Southern Biotech; the LB medium was purchased from hopebiol Co., Ltd.

    Techniques: Control, Injection, Comparison