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isotype matched control antibody  (R&D Systems)


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    R&D Systems isotype matched control antibody
    Isotype Matched Control Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 103 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/igg2b+isotype+control/Mouse+IgG2B+APC-conjugated+Antibody/us12613244-531-21-26
    Average 93 stars, based on 103 article reviews
    isotype matched control antibody - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection
    Article Snippet: Ex vivo LILRB1 and CD57 expression along T cell differentiation To assess CD57 and LILRB1 expression along T cell differentiation, CMV/pp65-specific CD8 T cell clonotypes of high versus low avidity isolated and stained as described in the main manuscript (CD8, CD28, CD45RA, CD57, CD85j, CMV/pp65 multimer, Vivid Aqua and appropriate TRBV antibodies (Supplementary Table 1)) were acquired on a Cytoflex flow cytometer (Beckman Coulter) and data were imported in FlowJo software (v.10.4.2, Tree Star) for analysis, using both CD28 and CD45RA as differentiation markers along which LILRB1 and CD57 positive cells were quantified as fractions of parent population. .. CFSE-labelled (Invitrogen) PBMCs from donor BCL4 were pulsed 1 hour at 37°C with native CMV/pp65495-503 peptide (10-8 M) washed and cultured in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT-2) blocking antibody or an IgG2B isotype control used at 5 μg/ml (R&D Systems). .. After 3-6 days, cells were washed, stained with Near-IR Vivid (Invitrogen), CMV/pp65-specific multimers, anti-CD8 antibodies (Beckman Coulter) and anti-TRBV antibodies specific for the TCRab clonotypes identified in BCL4 (Supplementary Table 1) before acquisition on a LSRII (BD Biosciences) cytometer.

    Recombinant:

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection
    Article Snippet: Ex vivo LILRB1 and CD57 expression along T cell differentiation To assess CD57 and LILRB1 expression along T cell differentiation, CMV/pp65-specific CD8 T cell clonotypes of high versus low avidity isolated and stained as described in the main manuscript (CD8, CD28, CD45RA, CD57, CD85j, CMV/pp65 multimer, Vivid Aqua and appropriate TRBV antibodies (Supplementary Table 1)) were acquired on a Cytoflex flow cytometer (Beckman Coulter) and data were imported in FlowJo software (v.10.4.2, Tree Star) for analysis, using both CD28 and CD45RA as differentiation markers along which LILRB1 and CD57 positive cells were quantified as fractions of parent population. .. CFSE-labelled (Invitrogen) PBMCs from donor BCL4 were pulsed 1 hour at 37°C with native CMV/pp65495-503 peptide (10-8 M) washed and cultured in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT-2) blocking antibody or an IgG2B isotype control used at 5 μg/ml (R&D Systems). .. After 3-6 days, cells were washed, stained with Near-IR Vivid (Invitrogen), CMV/pp65-specific multimers, anti-CD8 antibodies (Beckman Coulter) and anti-TRBV antibodies specific for the TCRab clonotypes identified in BCL4 (Supplementary Table 1) before acquisition on a LSRII (BD Biosciences) cytometer.

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection.
    Article Snippet: .. In vitro LILRB1 blocking experiments 30-Gy-irradiated HLA-A*0201-positive PBMCs were pulsed 1 hour at 37°C with the native CMV/pp65495-503 peptide (10 -8M), Frontiers in Immunology 04 washed, and incubated with CFSE-labelled (Invitrogen) CMV/ pp65-specific CD8 T cell clones of high or low avidity at an E/T ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT2) blocking antibody or an IgG2B isotype control used at 5 mg/ml (R&D Systems). .. After 3 days, cells were washed, stained in PBS with Near-IR Vivid (Invitrogen) at 4°C for 30 minutes before acquisition on a LSRII (BD Biosciences) cytometer.

    Blocking Assay:

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection
    Article Snippet: Ex vivo LILRB1 and CD57 expression along T cell differentiation To assess CD57 and LILRB1 expression along T cell differentiation, CMV/pp65-specific CD8 T cell clonotypes of high versus low avidity isolated and stained as described in the main manuscript (CD8, CD28, CD45RA, CD57, CD85j, CMV/pp65 multimer, Vivid Aqua and appropriate TRBV antibodies (Supplementary Table 1)) were acquired on a Cytoflex flow cytometer (Beckman Coulter) and data were imported in FlowJo software (v.10.4.2, Tree Star) for analysis, using both CD28 and CD45RA as differentiation markers along which LILRB1 and CD57 positive cells were quantified as fractions of parent population. .. CFSE-labelled (Invitrogen) PBMCs from donor BCL4 were pulsed 1 hour at 37°C with native CMV/pp65495-503 peptide (10-8 M) washed and cultured in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT-2) blocking antibody or an IgG2B isotype control used at 5 μg/ml (R&D Systems). .. After 3-6 days, cells were washed, stained with Near-IR Vivid (Invitrogen), CMV/pp65-specific multimers, anti-CD8 antibodies (Beckman Coulter) and anti-TRBV antibodies specific for the TCRab clonotypes identified in BCL4 (Supplementary Table 1) before acquisition on a LSRII (BD Biosciences) cytometer.

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection.
    Article Snippet: .. In vitro LILRB1 blocking experiments 30-Gy-irradiated HLA-A*0201-positive PBMCs were pulsed 1 hour at 37°C with the native CMV/pp65495-503 peptide (10 -8M), Frontiers in Immunology 04 washed, and incubated with CFSE-labelled (Invitrogen) CMV/ pp65-specific CD8 T cell clones of high or low avidity at an E/T ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT2) blocking antibody or an IgG2B isotype control used at 5 mg/ml (R&D Systems). .. After 3 days, cells were washed, stained in PBS with Near-IR Vivid (Invitrogen) at 4°C for 30 minutes before acquisition on a LSRII (BD Biosciences) cytometer.

    Control:

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection
    Article Snippet: Ex vivo LILRB1 and CD57 expression along T cell differentiation To assess CD57 and LILRB1 expression along T cell differentiation, CMV/pp65-specific CD8 T cell clonotypes of high versus low avidity isolated and stained as described in the main manuscript (CD8, CD28, CD45RA, CD57, CD85j, CMV/pp65 multimer, Vivid Aqua and appropriate TRBV antibodies (Supplementary Table 1)) were acquired on a Cytoflex flow cytometer (Beckman Coulter) and data were imported in FlowJo software (v.10.4.2, Tree Star) for analysis, using both CD28 and CD45RA as differentiation markers along which LILRB1 and CD57 positive cells were quantified as fractions of parent population. .. CFSE-labelled (Invitrogen) PBMCs from donor BCL4 were pulsed 1 hour at 37°C with native CMV/pp65495-503 peptide (10-8 M) washed and cultured in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT-2) blocking antibody or an IgG2B isotype control used at 5 μg/ml (R&D Systems). .. After 3-6 days, cells were washed, stained with Near-IR Vivid (Invitrogen), CMV/pp65-specific multimers, anti-CD8 antibodies (Beckman Coulter) and anti-TRBV antibodies specific for the TCRab clonotypes identified in BCL4 (Supplementary Table 1) before acquisition on a LSRII (BD Biosciences) cytometer.

    Article Title: Effect of Flavonoids on MCP-1 Expression in Human Coronary Artery Endothelial Cells and Impact on MCP-1-Dependent Migration of Human Monocytes
    Article Snippet: BD Pharmingen TM Recombinant Human MCP-1 (#554620) was purchased from BD Biosciences (Franklin Lakes, NJ, USA). .. IgG2B Isotype Control (#MAB004; RRID:AB_357346) and CCL2/JE/MCP-1 Antibody (#MAB679; RRID:AB_2071559) were obtained from R&D Systems (Wiesbaden, Germany). .. WST-1 ((4-[3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate) was bought from Roche Diagnostics (Mannheim, Germany).

    Article Title: Microfluidic-Based Reconstitution of Functional Lymphatic Microvasculature: Elucidating the Role of Lymphatics in Health and Disease.
    Article Snippet: In a similar set of experiments, Fluorescein-conjugated avidin (Thermofisher) or Alexa Fluor 647-conjugated albumin from bovine serum (Thermofisher) was introduced into the system at a concentration of 100 μg mL−1. .. For neutralizing antibody experiments, PBMCs were incubated in a buffer solution with their respective antibody blocker at a concentration of 5 μg mL−1: human CCR7 antibody (MAB197-SP, R&D), human CXCR4 antibody (MAB172-SP, R&D), and a combine human IgG2A and IgG2B isotype control (MAB003 and MAB004, R&D). .. Device Seeding and Microvascular Culture: Fibrinogen from bovine plasma (Sigma) was dissolved for at least 3 h at 37 °C in Dulbecco’s Phosphate-Buffered Saline (DPBS, Lonza) at 5 mg mL−1, twice the final concentration.

    Article Title: Effect of Flavonoids on MCP-1 Expression in Human Coronary Artery Endothelial Cells and Impact on MCP-1-Dependent Migration of Human Monocytes.
    Article Snippet: BD PharmingenTM Recombinant Human MCP-1 (#554620) was purchased from BD Biosciences (Franklin Lakes, NJ, USA). .. IgG2B Isotype Control (#MAB004; RRID:AB_357346) and CCL2/JE/MCP-1 Antibody (#MAB679; RRID:AB_2071559) were obtained from R&D Systems (Wiesbaden, Germany). .. WST-1 ((4-[3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate) was bought from Roche Diagnostics (Mannheim, Germany).

    Article Title: A KLF2-BMPER-Smad1/5 checkpoint regulates high fluid shear stress-mediated artery remodeling
    Article Snippet: BMPER (Abcam ab73900; IB 1:1000, IF 1:400), KLF4 (Abcam ab215036; IF 1:400). .. Antibodies for BMP9 (MAB3209, clone #360107), BMP10 (MAB2926, clone #462732), IgG2A isotype control (MAB003, clone #20102) and IgG2B isotype control (MAB004, clone #20116) were purchased from R&D Systems. ..

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection.
    Article Snippet: .. In vitro LILRB1 blocking experiments 30-Gy-irradiated HLA-A*0201-positive PBMCs were pulsed 1 hour at 37°C with the native CMV/pp65495-503 peptide (10 -8M), Frontiers in Immunology 04 washed, and incubated with CFSE-labelled (Invitrogen) CMV/ pp65-specific CD8 T cell clones of high or low avidity at an E/T ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT2) blocking antibody or an IgG2B isotype control used at 5 mg/ml (R&D Systems). .. After 3 days, cells were washed, stained in PBS with Near-IR Vivid (Invitrogen) at 4°C for 30 minutes before acquisition on a LSRII (BD Biosciences) cytometer.

    Article Title: A KLF2-BMPER-Smad1/5 checkpoint regulates high fluid shear stress-mediated artery remodeling.
    Article Snippet: Vascular remodeling to match arterial diameter to tissue requirements commonly fails in ischemic disease.. Endothelial cells sense fluid shear stress (FSS) from blood flow to maintain FSS within a narrow range in healthy vessels.. Thus, high FSS induces vessel outward remodeling, but mechanisms are poorly understood.

    Incubation:

    Article Title: Microfluidic-Based Reconstitution of Functional Lymphatic Microvasculature: Elucidating the Role of Lymphatics in Health and Disease.
    Article Snippet: In a similar set of experiments, Fluorescein-conjugated avidin (Thermofisher) or Alexa Fluor 647-conjugated albumin from bovine serum (Thermofisher) was introduced into the system at a concentration of 100 μg mL−1. .. For neutralizing antibody experiments, PBMCs were incubated in a buffer solution with their respective antibody blocker at a concentration of 5 μg mL−1: human CCR7 antibody (MAB197-SP, R&D), human CXCR4 antibody (MAB172-SP, R&D), and a combine human IgG2A and IgG2B isotype control (MAB003 and MAB004, R&D). .. Device Seeding and Microvascular Culture: Fibrinogen from bovine plasma (Sigma) was dissolved for at least 3 h at 37 °C in Dulbecco’s Phosphate-Buffered Saline (DPBS, Lonza) at 5 mg mL−1, twice the final concentration.

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection.
    Article Snippet: .. In vitro LILRB1 blocking experiments 30-Gy-irradiated HLA-A*0201-positive PBMCs were pulsed 1 hour at 37°C with the native CMV/pp65495-503 peptide (10 -8M), Frontiers in Immunology 04 washed, and incubated with CFSE-labelled (Invitrogen) CMV/ pp65-specific CD8 T cell clones of high or low avidity at an E/T ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT2) blocking antibody or an IgG2B isotype control used at 5 mg/ml (R&D Systems). .. After 3 days, cells were washed, stained in PBS with Near-IR Vivid (Invitrogen) at 4°C for 30 minutes before acquisition on a LSRII (BD Biosciences) cytometer.

    Concentration Assay:

    Article Title: Microfluidic-Based Reconstitution of Functional Lymphatic Microvasculature: Elucidating the Role of Lymphatics in Health and Disease.
    Article Snippet: In a similar set of experiments, Fluorescein-conjugated avidin (Thermofisher) or Alexa Fluor 647-conjugated albumin from bovine serum (Thermofisher) was introduced into the system at a concentration of 100 μg mL−1. .. For neutralizing antibody experiments, PBMCs were incubated in a buffer solution with their respective antibody blocker at a concentration of 5 μg mL−1: human CCR7 antibody (MAB197-SP, R&D), human CXCR4 antibody (MAB172-SP, R&D), and a combine human IgG2A and IgG2B isotype control (MAB003 and MAB004, R&D). .. Device Seeding and Microvascular Culture: Fibrinogen from bovine plasma (Sigma) was dissolved for at least 3 h at 37 °C in Dulbecco’s Phosphate-Buffered Saline (DPBS, Lonza) at 5 mg mL−1, twice the final concentration.

    In Vitro:

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection.
    Article Snippet: .. In vitro LILRB1 blocking experiments 30-Gy-irradiated HLA-A*0201-positive PBMCs were pulsed 1 hour at 37°C with the native CMV/pp65495-503 peptide (10 -8M), Frontiers in Immunology 04 washed, and incubated with CFSE-labelled (Invitrogen) CMV/ pp65-specific CD8 T cell clones of high or low avidity at an E/T ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT2) blocking antibody or an IgG2B isotype control used at 5 mg/ml (R&D Systems). .. After 3 days, cells were washed, stained in PBS with Near-IR Vivid (Invitrogen) at 4°C for 30 minutes before acquisition on a LSRII (BD Biosciences) cytometer.

    Clone Assay:

    Article Title: Overall avidity declines in TCR repertoires during latent CMV but not EBV infection.
    Article Snippet: .. In vitro LILRB1 blocking experiments 30-Gy-irradiated HLA-A*0201-positive PBMCs were pulsed 1 hour at 37°C with the native CMV/pp65495-503 peptide (10 -8M), Frontiers in Immunology 04 washed, and incubated with CFSE-labelled (Invitrogen) CMV/ pp65-specific CD8 T cell clones of high or low avidity at an E/T ratio of 1:1 in RPMI 1640 medium (Gibco) supplemented with 8% human serum and 50 U/ml human recombinant IL-2 (GlaxoSmithKline) in the presence of monoclonal IgG2B mouse anti-human LILRB1 (CD85j, ILT2) blocking antibody or an IgG2B isotype control used at 5 mg/ml (R&D Systems). .. After 3 days, cells were washed, stained in PBS with Near-IR Vivid (Invitrogen) at 4°C for 30 minutes before acquisition on a LSRII (BD Biosciences) cytometer.



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