tlr cells Search Results


tlr (cell surface) screening antibody pack  (Bio-Techne corporation)
90
Bio-Techne corporation tlr (cell surface) screening antibody pack
Tlr (Cell Surface) Screening Antibody Pack, supplied by Bio-Techne corporation, 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/result/tlr (cell surface) screening antibody pack/product/Bio-Techne corporation
Average 90 stars, based on 1 article reviews
tlr (cell surface) screening antibody pack - by Bioz Stars, 2026-02
90/100 stars
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hek-293 cells transfected with tlr-2  (Asterand Inc)
90
Asterand Inc hek-293 cells transfected with tlr-2
Hek 293 Cells Transfected With Tlr 2, supplied by Asterand Inc, 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/result/hek-293 cells transfected with tlr-2/product/Asterand Inc
Average 90 stars, based on 1 article reviews
hek-293 cells transfected with tlr-2 - by Bioz Stars, 2026-02
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cd14/toll-like receptor (tlr) 2 and 4  (Cell Genesys)
90
Cell Genesys cd14/toll-like receptor (tlr) 2 and 4
Cd14/Toll Like Receptor (Tlr) 2 And 4, supplied by Cell Genesys, 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/result/cd14/toll-like receptor (tlr) 2 and 4/product/Cell Genesys
Average 90 stars, based on 1 article reviews
cd14/toll-like receptor (tlr) 2 and 4 - by Bioz Stars, 2026-02
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murine macrophage tlr knockout cell lines δmyd88  (BEI Resources)
90
BEI Resources murine macrophage tlr knockout cell lines δmyd88
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Murine Macrophage Tlr Knockout Cell Lines δmyd88, supplied by BEI Resources, 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/result/murine macrophage tlr knockout cell lines δmyd88/product/BEI Resources
Average 90 stars, based on 1 article reviews
murine macrophage tlr knockout cell lines δmyd88 - by Bioz Stars, 2026-02
90/100 stars
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hek-blue tlr reporter cells hkb-mtlr4  (Innovagen AB)
90
Innovagen AB hek-blue tlr reporter cells hkb-mtlr4
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Hek Blue Tlr Reporter Cells Hkb Mtlr4, supplied by Innovagen AB, 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/result/hek-blue tlr reporter cells hkb-mtlr4/product/Innovagen AB
Average 90 stars, based on 1 article reviews
hek-blue tlr reporter cells hkb-mtlr4 - by Bioz Stars, 2026-02
90/100 stars
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tlr knockout cell lines  (BEI Resources)
90
BEI Resources tlr knockout cell lines
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Tlr Knockout Cell Lines, supplied by BEI Resources, 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/result/tlr knockout cell lines/product/BEI Resources
Average 90 stars, based on 1 article reviews
tlr knockout cell lines - by Bioz Stars, 2026-02
90/100 stars
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responses of dendritic cells to tlr-4 stimulation  (Janssen)
90
Janssen responses of dendritic cells to tlr-4 stimulation
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Responses Of Dendritic Cells To Tlr 4 Stimulation, supplied by Janssen, 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/result/responses of dendritic cells to tlr-4 stimulation/product/Janssen
Average 90 stars, based on 1 article reviews
responses of dendritic cells to tlr-4 stimulation - by Bioz Stars, 2026-02
90/100 stars
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human cell codon-optimized cdna corresponding to the predicted amino acid sequence of nv-tlr  (GenScript corporation)
90
GenScript corporation human cell codon-optimized cdna corresponding to the predicted amino acid sequence of nv-tlr
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Human Cell Codon Optimized Cdna Corresponding To The Predicted Amino Acid Sequence Of Nv Tlr, supplied by GenScript corporation, 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/result/human cell codon-optimized cdna corresponding to the predicted amino acid sequence of nv-tlr/product/GenScript corporation
Average 90 stars, based on 1 article reviews
human cell codon-optimized cdna corresponding to the predicted amino acid sequence of nv-tlr - by Bioz Stars, 2026-02
90/100 stars
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hek-tlr-4 yfp -md-2 cell line nr-9315  (BEI Resources)
90
BEI Resources hek-tlr-4 yfp -md-2 cell line nr-9315
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Hek Tlr 4 Yfp Md 2 Cell Line Nr 9315, supplied by BEI Resources, 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/result/hek-tlr-4 yfp -md-2 cell line nr-9315/product/BEI Resources
Average 90 stars, based on 1 article reviews
hek-tlr-4 yfp -md-2 cell line nr-9315 - by Bioz Stars, 2026-02
90/100 stars
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cdnas encoding human cell codon-optimized versions of of-nf-κb, ofikk, and of-tlr  (GenScript corporation)
90
GenScript corporation cdnas encoding human cell codon-optimized versions of of-nf-κb, ofikk, and of-tlr
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Cdnas Encoding Human Cell Codon Optimized Versions Of Of Nf κb, Ofikk, And Of Tlr, supplied by GenScript corporation, 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/result/cdnas encoding human cell codon-optimized versions of of-nf-κb, ofikk, and of-tlr/product/GenScript corporation
Average 90 stars, based on 1 article reviews
cdnas encoding human cell codon-optimized versions of of-nf-κb, ofikk, and of-tlr - by Bioz Stars, 2026-02
90/100 stars
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characterization effective tlr agonist, t-cell helper peptide, diameter % w/w % w/w nanocarrier 217 ova  (NanoCarrier Co)
90
NanoCarrier Co characterization effective tlr agonist, t-cell helper peptide, diameter % w/w % w/w nanocarrier 217 ova
The innate immune receptor <t>TLR2</t> and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.
Characterization Effective Tlr Agonist, T Cell Helper Peptide, Diameter % W/W % W/W Nanocarrier 217 Ova, supplied by NanoCarrier Co, 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/result/characterization effective tlr agonist, t-cell helper peptide, diameter % w/w % w/w nanocarrier 217 ova/product/NanoCarrier Co
Average 90 stars, based on 1 article reviews
characterization effective tlr agonist, t-cell helper peptide, diameter % w/w % w/w nanocarrier 217 ova - by Bioz Stars, 2026-02
90/100 stars
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Image Search Results


The innate immune receptor TLR2 and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.

Journal: Frontiers in Immunology

Article Title: Deciphering the functional roles of PE18 and PPE26 proteins in modulating Mycobacterium tuberculosis pathogenesis and immune response

doi: 10.3389/fimmu.2025.1517822

Figure Lengend Snippet: The innate immune receptor TLR2 and adaptor Myd88 are involved in the secretion of proinflammatory cytokines. (A-C) 6-well tissue culture plates were used for seeding 2 million TLR knockout macrophage cells. The cells were incubated overnight for adherence. After adherence, cells were infected with Msmeg , Msmeg_VC , and Msmeg expressing PE18, PPE26, and PE18+PPE26 (MOI = 1:10). Culture supernatants were collected after 24 and 48 h of infection. The levels of TNFα, IL6, and IL12 were quantified using ELISA. (D-F) 6-well culture plates were used for seeding ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88 mouse macrophages (2 million cells/well) and allowed to adhere for 2 h. PE18 (5 µg), PPE26 (5 µg), and PE18 (2. 5µg) + PPE26 (2.5 µg) purified proteins were used to treat macrophage cells for 24 h. The culture supernatant was collected, and TNFα, IL6, and IL12 levels were measured using sandwich ELISA. Untreated (UT) cells, Proteinase K-digested, and heat-inactivated protein (HI) (5 µg)-treated cells were used as negative controls. Three independent experiments were performed to determine the level of pro-inflammatory cytokines. ****P values less than 0.0001 as compared to the controls. n. s shows that the data were not significant.

Article Snippet: The Biodefense and Emerging Infections Research (BEI) resources (NIAID, NIH) provided the murine macrophage TLR knockout cell lines ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88.

Techniques: Knock-Out, Incubation, Infection, Expressing, Enzyme-linked Immunosorbent Assay, Purification, Sandwich ELISA

Mtb PE18 and PPE26 employ TLR2 and Myd88 for regulating immune response and endosome-phagosome maturation: A Model. Mtb PE18 and PPE26 heterodimers interact with the innate immune receptor TLR2, recruiting adapter Myd88 to initiating downstream signaling cascades and the consequent secretion of proinflammatory cytokines and NO. PE18 and PPE26 primed peritoneal macrophages and splenocytes showed increased expression of activation markers, proinflammatory cytokine production, and skewed memory response towards T-cells cell-mediated effector memory. PE18 and PPE26 proteins inhibit actin-mediated cytoskeleton dynamics by regulating the protein levels of Arp2, N-Wasp, Profilin, and Rac1. In addition to the regulation of actin dynamics, PE18 and PPE26 possibly hampers endosome-phagosome maturation by modulating the early, late, and recycling endosome markers EEA1, Rab5, Rab7, and Rab11. These findings highlight that Mtb PE18 and PPE26 mediated subversion of innate defenses leads to efficient survival and virulence.

Journal: Frontiers in Immunology

Article Title: Deciphering the functional roles of PE18 and PPE26 proteins in modulating Mycobacterium tuberculosis pathogenesis and immune response

doi: 10.3389/fimmu.2025.1517822

Figure Lengend Snippet: Mtb PE18 and PPE26 employ TLR2 and Myd88 for regulating immune response and endosome-phagosome maturation: A Model. Mtb PE18 and PPE26 heterodimers interact with the innate immune receptor TLR2, recruiting adapter Myd88 to initiating downstream signaling cascades and the consequent secretion of proinflammatory cytokines and NO. PE18 and PPE26 primed peritoneal macrophages and splenocytes showed increased expression of activation markers, proinflammatory cytokine production, and skewed memory response towards T-cells cell-mediated effector memory. PE18 and PPE26 proteins inhibit actin-mediated cytoskeleton dynamics by regulating the protein levels of Arp2, N-Wasp, Profilin, and Rac1. In addition to the regulation of actin dynamics, PE18 and PPE26 possibly hampers endosome-phagosome maturation by modulating the early, late, and recycling endosome markers EEA1, Rab5, Rab7, and Rab11. These findings highlight that Mtb PE18 and PPE26 mediated subversion of innate defenses leads to efficient survival and virulence.

Article Snippet: The Biodefense and Emerging Infections Research (BEI) resources (NIAID, NIH) provided the murine macrophage TLR knockout cell lines ΔTLR2, ΔTLR4, ΔTRIF, and ΔMyd88.

Techniques: Expressing, Activation Assay