rabbit anti human ifn c Search Results


rabbit anti human ifn c  (Bio-Rad)
85
Bio-Rad rabbit anti human ifn c
Rabbit Anti Human Ifn C, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ifn c igg antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology ifn c igg antibody
Ifn C Igg Antibody, 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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recombinant human interferon c ifnc  (R&D Systems)
94
R&D Systems recombinant human interferon c ifnc
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Recombinant Human Interferon C Ifnc, supplied by R&D Systems, 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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Average 94 stars, based on 1 article reviews
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rabbit anti human ifn c pab  (Novus Biologicals)
90
Novus Biologicals rabbit anti human ifn c pab
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Rabbit Anti Human Ifn C Pab, 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
https://www.bioz.com/product/rabbit+anti+human+ifn+c/Rabbit+anti-Human+IgA+Fc+Secondary+Antibody/10__1161_slash_jaha__117__008145-35-26-30
Average 90 stars, based on 1 article reviews
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polyclonal goat anti human ifn c  (R&D Systems)
92
R&D Systems polyclonal goat anti human ifn c
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Polyclonal Goat Anti Human Ifn C, supplied by R&D Systems, 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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mouse anti ifn c  (R&D Systems)
93
R&D Systems mouse anti ifn c
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Mouse Anti Ifn C, supplied by R&D Systems, 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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anti ifn c receptor b rabbit polyclonal antibody  (Santa Cruz Biotechnology)
95
Santa Cruz Biotechnology anti ifn c receptor b rabbit polyclonal antibody
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Anti Ifn C Receptor B Rabbit Polyclonal Antibody, supplied by Santa Cruz Biotechnology, 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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mb recombinant mouse ifn c carrier free biolegend  (R&D Systems)
95
R&D Systems mb recombinant mouse ifn c carrier free biolegend
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Mb Recombinant Mouse Ifn C Carrier Free Biolegend, supplied by R&D Systems, 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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ifn c  (Boster Bio)
91
Boster Bio ifn c
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Ifn C, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+human+ifn+c/Anti-Phospho-Interferon-alpha+Receptor%2C+Type+I%2C+Subunit+1+(Ser535%2C539)+Antibody/pm21538928-72-49-51
Average 91 stars, based on 1 article reviews
ifn c - by Bioz Stars, 2026-09
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recombinant human ifn c  (R&D Systems)
94
R&D Systems recombinant human ifn c
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Recombinant Human Ifn C, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+human+ifn+c/Recombinant+Human+IFN-epsilon+Protein/pm19250634-44-0-10
Average 94 stars, based on 1 article reviews
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recombinant human ifn-c  (Becton Dickinson)
90
Becton Dickinson recombinant human ifn-c
Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of <t>IFNc</t> or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.
Recombinant Human Ifn C, 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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Image Search Results


Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of IFNc or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.

Journal: Journal of neurochemistry

Article Title: Enhanced expression and shedding of the transmembrane chemokine CXCL16 by reactive astrocytes and glioma cells.

doi: 10.1111/j.1471-4159.2005.03123.x

Figure Lengend Snippet: Fig. 3 Induction of CXCL16 mRNA expression by proinflammatory cytokines in vitro. Cultured human endothelial cells and U343 glioma cells were stimulated with either 10 ng/mL of IFNc or TNFa alone or a combination of the two cytokines. After 24 h of incubation, the CXCL16 mRNA level was quantified by TaqMan RT-PCR and expressed as the percentage of that determined for the non-stimulated control. The expression of GAPDH mRNA was not affected by cell stimulation (not shown). Data are presented as means and SD of one representative of three independent experiments each performed in triplicates.

Article Snippet: Recombinant human CXCL16 extracellular domain and chemokine domain, recombinant human interferon-c (IFNc), recombinant human tumour necrosis factor-a (TNFa) as well as unconjugated goat antihuman CXCL16 antibody were obtained from R & D Systems (Wiesbaden, Germany).

Techniques: Expressing, In Vitro, Cell Culture, Incubation, Reverse Transcription Polymerase Chain Reaction, Control, Cell Stimulation

Fig. 4 Expression and release of CXCL16 protein. (a) Glioma cells were left untreated or stimulated with IFNc and TNFa for 24 h. Sub- sequently, the cells were washed and cell extracts prepared with Tri- ton-X100 were analysed by Western blotting with a rabbit antibody against human CXCL16. As a control, extracts of COS7 cells trans- fected with hemagglutinin (HA)-tagged CXCL16 were analysed in parallel. The transfected CXCL16 was detected by both, an anti-HA and the anti-CXCL16 antibody. Broad bands of the glycosylated transmembrane form of CXCL16 are visible at 49 kDa, the expression is stimulated by cytokine treatment. (b) The human glioma cell line (U 343) and glioma cells cultivated from a grade IV surgical glioma (A 761) were treated with IFNc (10 ng/mL), TNFa (10 ng/mL) glutamate (10 mM), substance p (10 nM), EGF (10 ng/mL), TGFb1 (10 ng/mL) and HIL-6 (10 ng/mL), for 24 h, and subsequently conditioned media were harvested and analysed for the presence of soluble CXCL16 by ELISA. Data are shown as means and SD of one representative of three independent experiments each performed in triplicates.

Journal: Journal of neurochemistry

Article Title: Enhanced expression and shedding of the transmembrane chemokine CXCL16 by reactive astrocytes and glioma cells.

doi: 10.1111/j.1471-4159.2005.03123.x

Figure Lengend Snippet: Fig. 4 Expression and release of CXCL16 protein. (a) Glioma cells were left untreated or stimulated with IFNc and TNFa for 24 h. Sub- sequently, the cells were washed and cell extracts prepared with Tri- ton-X100 were analysed by Western blotting with a rabbit antibody against human CXCL16. As a control, extracts of COS7 cells trans- fected with hemagglutinin (HA)-tagged CXCL16 were analysed in parallel. The transfected CXCL16 was detected by both, an anti-HA and the anti-CXCL16 antibody. Broad bands of the glycosylated transmembrane form of CXCL16 are visible at 49 kDa, the expression is stimulated by cytokine treatment. (b) The human glioma cell line (U 343) and glioma cells cultivated from a grade IV surgical glioma (A 761) were treated with IFNc (10 ng/mL), TNFa (10 ng/mL) glutamate (10 mM), substance p (10 nM), EGF (10 ng/mL), TGFb1 (10 ng/mL) and HIL-6 (10 ng/mL), for 24 h, and subsequently conditioned media were harvested and analysed for the presence of soluble CXCL16 by ELISA. Data are shown as means and SD of one representative of three independent experiments each performed in triplicates.

Article Snippet: Recombinant human CXCL16 extracellular domain and chemokine domain, recombinant human interferon-c (IFNc), recombinant human tumour necrosis factor-a (TNFa) as well as unconjugated goat antihuman CXCL16 antibody were obtained from R & D Systems (Wiesbaden, Germany).

Techniques: Expressing, Western Blot, Control, Transfection, Enzyme-linked Immunosorbent Assay