anti human cd69 pe Search Results


elabscience cat e ab f1138h  (Elabscience Biotechnology)
93
Elabscience Biotechnology elabscience cat e ab f1138h
Elabscience Cat E Ab F1138h, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+human+cd69+pe/PE%2FCyanine7+Anti-Human+CD69+Antibody/10__2147_slash_jir__s473068-77-104-104
Average 93 stars, based on 1 article reviews
elabscience cat e ab f1138h - by Bioz Stars, 2026-09
93/100 stars
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cd69  (Elabscience Biotechnology)
93
Elabscience Biotechnology cd69
(A). (i) Expression of Pf GBP-130 ECD fused with Transferrin membrane domain on the membrane of CHO K1 cells by infecting the lentiviral vector; pMSCV Puro and its immunofluorescence analysis using anti-rabbit Pf GBP antibody. (ii) CHO K1 cells expressing Pf GBP-130 ECD bind LFA-1 αI-Fc. Binding of purified LFA-1 αI-Fc to Pf GBP-130 ECD expressing CHO cells was assessed by FACS using an PE-Texas red anti-human IgG antibody. (B) NK cells activation in the presence of CHO K1 cells expressing Pf GBP ECD. Human NK cells were purified (>95%) from fresh PBMC and co-cultured with CHO K1 cells expressing Pf GBP ECD in 2: 1 ratio (20,000 CHO-K1 cells:10,000 NK cells) and these cells were stimulated with (Poly I:C/lipofectamine 2000) for 24 h. NK cells were separated from adherent CHO K1 cells and NK cells activation was assessed by assaying the expression of activation markers <t>(CD69,</t> CD25) and a degranulation marker; CD107a. NK cells co-cultured with CHO K1 cells expressing Pf GBP-ECD protein showed significant increase in the expression of CD25 and CD69, as well as CD107a in comparison to the NK cells co-cultured with mock CHO cells. Addition of anti-CD11a (HI111 clone) antibodies reduced the expression of both activation and degranulation markers. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.
Cd69, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+human+cd69+pe/PE+Anti-Human+CD69+Antibody/bio_rxiv__2025__08__20__671208-233-53-55
Average 93 stars, based on 1 article reviews
cd69 - by Bioz Stars, 2026-09
93/100 stars
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pe anti human cd69 antibody  (Cytek Biosciences)
92
Cytek Biosciences pe anti human cd69 antibody
(A). (i) Expression of Pf GBP-130 ECD fused with Transferrin membrane domain on the membrane of CHO K1 cells by infecting the lentiviral vector; pMSCV Puro and its immunofluorescence analysis using anti-rabbit Pf GBP antibody. (ii) CHO K1 cells expressing Pf GBP-130 ECD bind LFA-1 αI-Fc. Binding of purified LFA-1 αI-Fc to Pf GBP-130 ECD expressing CHO cells was assessed by FACS using an PE-Texas red anti-human IgG antibody. (B) NK cells activation in the presence of CHO K1 cells expressing Pf GBP ECD. Human NK cells were purified (>95%) from fresh PBMC and co-cultured with CHO K1 cells expressing Pf GBP ECD in 2: 1 ratio (20,000 CHO-K1 cells:10,000 NK cells) and these cells were stimulated with (Poly I:C/lipofectamine 2000) for 24 h. NK cells were separated from adherent CHO K1 cells and NK cells activation was assessed by assaying the expression of activation markers <t>(CD69,</t> CD25) and a degranulation marker; CD107a. NK cells co-cultured with CHO K1 cells expressing Pf GBP-ECD protein showed significant increase in the expression of CD25 and CD69, as well as CD107a in comparison to the NK cells co-cultured with mock CHO cells. Addition of anti-CD11a (HI111 clone) antibodies reduced the expression of both activation and degranulation markers. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.
Pe Anti Human Cd69 Antibody, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+human+cd69+pe/PE-Cyanine7+Anti-Human+CD69/pm36656150__ja2c10903_si_001-85-36-58
Average 92 stars, based on 1 article reviews
pe anti human cd69 antibody - by Bioz Stars, 2026-09
92/100 stars
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anti-human cd69 pe (holzel diagnostika)  (Holzel Diagnostika)
90
Holzel Diagnostika anti-human cd69 pe (holzel diagnostika)
(A). (i) Expression of Pf GBP-130 ECD fused with Transferrin membrane domain on the membrane of CHO K1 cells by infecting the lentiviral vector; pMSCV Puro and its immunofluorescence analysis using anti-rabbit Pf GBP antibody. (ii) CHO K1 cells expressing Pf GBP-130 ECD bind LFA-1 αI-Fc. Binding of purified LFA-1 αI-Fc to Pf GBP-130 ECD expressing CHO cells was assessed by FACS using an PE-Texas red anti-human IgG antibody. (B) NK cells activation in the presence of CHO K1 cells expressing Pf GBP ECD. Human NK cells were purified (>95%) from fresh PBMC and co-cultured with CHO K1 cells expressing Pf GBP ECD in 2: 1 ratio (20,000 CHO-K1 cells:10,000 NK cells) and these cells were stimulated with (Poly I:C/lipofectamine 2000) for 24 h. NK cells were separated from adherent CHO K1 cells and NK cells activation was assessed by assaying the expression of activation markers <t>(CD69,</t> CD25) and a degranulation marker; CD107a. NK cells co-cultured with CHO K1 cells expressing Pf GBP-ECD protein showed significant increase in the expression of CD25 and CD69, as well as CD107a in comparison to the NK cells co-cultured with mock CHO cells. Addition of anti-CD11a (HI111 clone) antibodies reduced the expression of both activation and degranulation markers. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.
Anti Human Cd69 Pe (Holzel Diagnostika), supplied by Holzel Diagnostika, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+human+cd69+pe/anti+human+cd69+pe/pmc00520823-58-28-33
Average 90 stars, based on 1 article reviews
anti-human cd69 pe (holzel diagnostika) - by Bioz Stars, 2026-09
90/100 stars
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pe cy 7 mouse anti human cd69  (BD Biosciences)
N/A
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pe cyanine7 anti human cd69  (Tonbo Biosciences)
N/A
PE CYANINE7 ANTI HUMAN CD69 FN50
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anti human cd8 fitc cd69 pe cd3 percp  (BD Biosciences)
N/A
The CD8 antibody clone SK1 is derived from hybridization of NS 1 mouse myeloma cells with spleen cells from BALB c mice immunized with human peripheral blood T lymphocytes The CD8 antibody clone SK1 is
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anti human il 2 fitc cd69 pe cd4 percp cy 5 5 cd3 apc  (BD Biosciences)
N/A
Anti Hu IL 2 clone 5344 111 is derived from a fusion of Sp2 0 myeloma cells with splenocytes from BALB c mice immunized with recombinant human IL 2 Anti Hu IL 2 clone 5344
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pe/cy7 anti-human cd69  (BioLegend)
N/A
PE/Cy7 anti-human CD69 [FN50]; Isotype: Mouse IgG1, κ; Reactivity: Human, Cross-Reactivity: Chimpanzee, Baboon, Cynomolgus, Rhesus, Pigtailed Macaque; Apps: FC; Size: 25 tests
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pe anti-human cd69  (BioLegend)
N/A
PE anti-human CD69 [FN50]; Isotype: Mouse IgG1, κ; Reactivity: Human, Cross-Reactivity: Chimpanzee, Baboon, Cynomolgus, Rhesus, Pigtailed Macaque; Apps: FC; Size: 25 tests
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anti human cd69 pe cd3 percp  (BD Biosciences)
N/A
CD69 clone L78 is derived from hybridization of mouse Sp2 0 Ag14 myeloma cells with lymph node cells from BALB c mice immunized with a CD8 alloantigen directed cytotoxic T lymphocyte CTL cell line CD69
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pe/cyanine5 anti-human cd69 antibody  (Elabscience Biotechnology)
N/A
CD69 is a 27-33 kD type II transmembrane protein also known as activation inducer molecule (AIM), very early activation antigen (VEA), and MLR3. It is a member of the C-type lectin family, expressed as a
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(A). (i) Expression of Pf GBP-130 ECD fused with Transferrin membrane domain on the membrane of CHO K1 cells by infecting the lentiviral vector; pMSCV Puro and its immunofluorescence analysis using anti-rabbit Pf GBP antibody. (ii) CHO K1 cells expressing Pf GBP-130 ECD bind LFA-1 αI-Fc. Binding of purified LFA-1 αI-Fc to Pf GBP-130 ECD expressing CHO cells was assessed by FACS using an PE-Texas red anti-human IgG antibody. (B) NK cells activation in the presence of CHO K1 cells expressing Pf GBP ECD. Human NK cells were purified (>95%) from fresh PBMC and co-cultured with CHO K1 cells expressing Pf GBP ECD in 2: 1 ratio (20,000 CHO-K1 cells:10,000 NK cells) and these cells were stimulated with (Poly I:C/lipofectamine 2000) for 24 h. NK cells were separated from adherent CHO K1 cells and NK cells activation was assessed by assaying the expression of activation markers (CD69, CD25) and a degranulation marker; CD107a. NK cells co-cultured with CHO K1 cells expressing Pf GBP-ECD protein showed significant increase in the expression of CD25 and CD69, as well as CD107a in comparison to the NK cells co-cultured with mock CHO cells. Addition of anti-CD11a (HI111 clone) antibodies reduced the expression of both activation and degranulation markers. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.

Journal: bioRxiv

Article Title: LFA-1 Interaction with GBP-130 on Plasmodium falciparum -infected Red Blood Cells mediates NK Cell Activation and Parasite Control

doi: 10.1101/2025.08.20.671208

Figure Lengend Snippet: (A). (i) Expression of Pf GBP-130 ECD fused with Transferrin membrane domain on the membrane of CHO K1 cells by infecting the lentiviral vector; pMSCV Puro and its immunofluorescence analysis using anti-rabbit Pf GBP antibody. (ii) CHO K1 cells expressing Pf GBP-130 ECD bind LFA-1 αI-Fc. Binding of purified LFA-1 αI-Fc to Pf GBP-130 ECD expressing CHO cells was assessed by FACS using an PE-Texas red anti-human IgG antibody. (B) NK cells activation in the presence of CHO K1 cells expressing Pf GBP ECD. Human NK cells were purified (>95%) from fresh PBMC and co-cultured with CHO K1 cells expressing Pf GBP ECD in 2: 1 ratio (20,000 CHO-K1 cells:10,000 NK cells) and these cells were stimulated with (Poly I:C/lipofectamine 2000) for 24 h. NK cells were separated from adherent CHO K1 cells and NK cells activation was assessed by assaying the expression of activation markers (CD69, CD25) and a degranulation marker; CD107a. NK cells co-cultured with CHO K1 cells expressing Pf GBP-ECD protein showed significant increase in the expression of CD25 and CD69, as well as CD107a in comparison to the NK cells co-cultured with mock CHO cells. Addition of anti-CD11a (HI111 clone) antibodies reduced the expression of both activation and degranulation markers. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.

Article Snippet: The following antibodies were used for staining: anti-human CD3 (biotin, OKT3; Elabsciences), anti CD16 (3G8; Biolegend), anti CD11a (HI111; BioLegend), CD56-PE (5.1H11; Elabsciences), Ultra-LEAFTM Purified Human IgG1 Isotype (Biolegend), Goat anti-Human IgG Alexa FluorTM 488 (Invitrogen), Goat anti-Human IgG Secondary Antibody, Alexa FluorTM 594 (Invitrogen), (CD107a (H4A3; Elabsciences), CD25-Alexa Fluor® 488 (BioLegend), and CD69 (FN50; Elabsciences).

Techniques: Expressing, Membrane, Plasmid Preparation, Immunofluorescence, Binding Assay, Purification, Activation Assay, Cell Culture, Marker, Comparison

(A) Activated human NK cells eliminate iRBCs in vitro. Human NK cells when co-cultured with iRBCs reduce parasitemia significantly after 96h and in the presence of anti- Pf GBP-130 antibodies this reduction in parasitemia was blocked. Presence of anti-GBP-130 abs resulted in parasitemia simialr to the control when NK cells were incubated with iRBCs alone. (B) NK cells activation in the presence of iRBCs. Human NK cells were were purified (>95%) from fresh PBMC and co-cultured with synchronized schizont stage iRBCs at a parasitemia of 0.5% in 10:1 ratio (NK: iRBC) for 48h. Quantification of activation and degranulation markers was performed after 48 hours. NK cells co-cultured with iRBCs showed significant increase in the expression of CD25 and CD69, the two activation markers as well as for the expression of CD107a, a degranulation marker in comparison to the NK cells co-cultured with RBCs alone. Addition of anti-rabbit PfGBP-130 antibodies reduced the expression of both activation and degranulation markers in these NK cells in comparison to rabbit IgG isotype control. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.

Journal: bioRxiv

Article Title: LFA-1 Interaction with GBP-130 on Plasmodium falciparum -infected Red Blood Cells mediates NK Cell Activation and Parasite Control

doi: 10.1101/2025.08.20.671208

Figure Lengend Snippet: (A) Activated human NK cells eliminate iRBCs in vitro. Human NK cells when co-cultured with iRBCs reduce parasitemia significantly after 96h and in the presence of anti- Pf GBP-130 antibodies this reduction in parasitemia was blocked. Presence of anti-GBP-130 abs resulted in parasitemia simialr to the control when NK cells were incubated with iRBCs alone. (B) NK cells activation in the presence of iRBCs. Human NK cells were were purified (>95%) from fresh PBMC and co-cultured with synchronized schizont stage iRBCs at a parasitemia of 0.5% in 10:1 ratio (NK: iRBC) for 48h. Quantification of activation and degranulation markers was performed after 48 hours. NK cells co-cultured with iRBCs showed significant increase in the expression of CD25 and CD69, the two activation markers as well as for the expression of CD107a, a degranulation marker in comparison to the NK cells co-cultured with RBCs alone. Addition of anti-rabbit PfGBP-130 antibodies reduced the expression of both activation and degranulation markers in these NK cells in comparison to rabbit IgG isotype control. * Denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001.

Article Snippet: The following antibodies were used for staining: anti-human CD3 (biotin, OKT3; Elabsciences), anti CD16 (3G8; Biolegend), anti CD11a (HI111; BioLegend), CD56-PE (5.1H11; Elabsciences), Ultra-LEAFTM Purified Human IgG1 Isotype (Biolegend), Goat anti-Human IgG Alexa FluorTM 488 (Invitrogen), Goat anti-Human IgG Secondary Antibody, Alexa FluorTM 594 (Invitrogen), (CD107a (H4A3; Elabsciences), CD25-Alexa Fluor® 488 (BioLegend), and CD69 (FN50; Elabsciences).

Techniques: In Vitro, Cell Culture, Control, Incubation, Activation Assay, Purification, Expressing, Marker, Comparison