anti abca1 pe Search Results


95
Bio-Techne corporation abca1 antibody - bsa free
Abca1 Antibody Bsa Free, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
Novus Biologicals anti abca1 antibody pe cy7
Anti Abca1 Antibody Pe Cy7, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson pe-conjugated mouse anti- hla-abc
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Pe Conjugated Mouse Anti Hla Abc, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
Proteintech anti cd68
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Anti Cd68, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Santa Cruz Biotechnology staining with fitc fluorescein isothiocyanate labeled anti abca1
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Staining With Fitc Fluorescein Isothiocyanate Labeled Anti Abca1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Becton Dickinson cd163-pe
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Cd163 Pe, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Santa Cruz Biotechnology apc cd11b
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Apc Cd11b, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Becton Dickinson fitc-conjugated anti-mouse cd14 antibody
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Fitc Conjugated Anti Mouse Cd14 Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioss bs-0024r-pe-cy3
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Bs 0024r Pe Cy3, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gapdh  (Abcam)
99
Abcam gapdh
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Gapdh, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioss bs-0024r-pe-cy7
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Bs 0024r Pe Cy7, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioss bs-0024r-pe
iPSCs are vulnerable to complement activation. (A) <t>HLA-ABC</t> surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Bs 0024r Pe, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


iPSCs are vulnerable to complement activation. (A) HLA-ABC surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.

Journal: Frontiers in Immunology

Article Title: Inhibition of complement activation by CD55 overexpression in human induced pluripotent stem cell derived kidney organoids

doi: 10.3389/fimmu.2022.1058763

Figure Lengend Snippet: iPSCs are vulnerable to complement activation. (A) HLA-ABC surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.

Article Snippet: For flow cytometry the following antibodies were used: PE-conjugated mouse anti- HLA-ABC (1:100, 555553, BD Biosciences), human anti- HLA-A2 antibody (3 µg mL -1 , SN607D8), mouse anti-human CD55 (1:500, ab1422, Abcam), mouse anti-C3 (1:1000, RFK22, in-house generated), mouse anti-C5b-9 (1:100, AE11, Hycult Biotech), PE-conjugated mouse anti-human CD46 (1:100, 12-0469-42, Invitrogen), and APC-conjugated mouse anti-human CD59 (1:100, 17-0596-42, Invitrogen) were used as primary antibodies.

Techniques: Activation Assay, Expressing, Flow Cytometry, Quantitative RT-PCR, In Vitro, Incubation, Fluorescence, Standard Deviation