free ca 2 Search Results


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Novus Biologicals rabbit polyclonal anti xbp1
Rabbit Polyclonal Anti Xbp1, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals tnfα neutralizing antibody infliximab
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Novus Biologicals infliximab
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Infliximab, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Alomone Labs primary antibodies against ncx1
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Primary Antibodies Against Ncx1, supplied by Alomone Labs, 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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Novus Biologicals anti carbonic anhydrase ii
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Anti Carbonic Anhydrase Ii, supplied by Novus Biologicals, 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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Corning Life Sciences hanks’ balanced salt solution with ca 2+ and 2
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Hanks’ Balanced Salt Solution With Ca 2+ And 2, supplied by Corning Life Sciences, 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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Biochrom hbss without ca2 and mg2
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
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BioWhittaker Molecular Applications ca2 -free eagle’s minimal essential medium (emem)
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Ca2 Free Eagle’s Minimal Essential Medium (Emem), supplied by BioWhittaker Molecular Applications, 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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BioWhittaker Molecular Applications endotoxin-free pbs without ca 2+ and 2
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Endotoxin Free Pbs Without Ca 2+ And 2, supplied by BioWhittaker Molecular Applications, 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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BioIVT Inc 1 ml 37°c ca 2+ /mg 2+ -free hbss (with 1 mm egta)
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
1 Ml 37°C Ca 2+ /Mg 2+ Free Hbss (With 1 Mm Egta), supplied by BioIVT Inc, 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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1 ml 37°c ca 2+ /mg 2+ -free hbss (with 1 mm egta) - by Bioz Stars, 2026-11
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Welgene inc calcium and magnesium-free hanks’ balanced salt solution hbss
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Calcium And Magnesium Free Hanks’ Balanced Salt Solution Hbss, supplied by Welgene inc, 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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Cook Canada Inc ca 2+ 2+ -free medium
WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα <t>(infliximab</t> (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.
Ca 2+ 2+ Free Medium, supplied by Cook Canada Inc, 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


WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα (infliximab (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.

Journal: The Journal of Biological Chemistry

Article Title: Matrix metalloproteinases inactivate the proinflammatory functions of secreted moonlighting tryptophanyl-tRNA synthetase

doi: 10.1074/jbc.RA119.009584

Figure Lengend Snippet: WRS increases MMP activity in macrophage-conditioned media by a TNFα-dependent pathway. PMA-differentiated THP1-derived macrophages were treated for 24 h with recombinant human WRS (100 nm), Δ1–47 WRS (100 nm) as an analog of the MMP7 and MMP8 cleavage product, TNFα (40 ng/ml), or buffer with or without a mAb inhibitor of TNFα (infliximab (IN)) (100 ng/ml). MMPs in 20-fold–concentrated conditioned media were activated with 1 mm APMA, and cleavage of the quenched fluorescence peptide substrate Mca-Pro-Leu-Gly↓Leu-Dpa-Ala-Arg-NH2 was measured (scatter plots show means ± S.D., n = 3) in N = 3 independent experiments. Statistical significance was determined against buffer + infliximab using a one-way ANOVA with Dunnett's multiple comparison posttests. ***, p < 0.001; ns, not significant. Error bars represent S.D.

Article Snippet: To assess MMP activity in conditioned medium, THP1 M0 cells were cultured in phenol red–free, serum-free growth medium for 24 h with 10 μg/ml polymyxin B plus 100 n m WRS, TNFα 40 μg/ml, or PBS ± 100 μg/ml infliximab (Novus Biologicals, catalog number NBP2-52655).

Techniques: Activity Assay, Derivative Assay, Recombinant, Fluorescence, Comparison