biotinylated anti il 8 ab (R&D Systems)
Structured Review

Biotinylated Anti Il 8 Ab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 135 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/biotinylated anti il 8 ab/product/R&D Systems
Average 93 stars, based on 135 article reviews
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1) Product Images from "Thrombin Regulates Chemokine Induction during Human Retinal Pigment Epithelial Cell/Monocyte Interaction"
Article Title: Thrombin Regulates Chemokine Induction during Human Retinal Pigment Epithelial Cell/Monocyte Interaction
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Figure Legend Snippet: Modulation of IL-8 (A), MCP-1 (B), and IL-6 (C) secretion by IFN-γ. HRPE cells (HRPE), monocytes (Mo), and HRPE cell/monocyte co-cultures (HRPE + Mo) were incubated in the medium containing IFN-γ (1000 U/ml), either alone or in combination with thrombin for 24 hours. Supernatants were collected and IL-8, MCP-1, and IL-6 protein levels in supernatants were measured by ELISA (n = 3).
Techniques Used: Incubation, Enzyme-linked Immunosorbent Assay
Figure Legend Snippet: Thrombin induction of HRPE IL-8 and MCP-1 mRNA. A: HRPE cells were incubated with thrombin (10 U/ml) for different times, total RNA was extracted, and semiquantitative RT-PCR was performed. These representative data are from one of three independent experiments. B: Results are expressed as a ratio of each PCR product/β-actin band density. Values represent means ± SEM (n = 3).
Techniques Used: Incubation, Reverse Transcription Polymerase Chain Reaction
Figure Legend Snippet: Thrombin modulated cell-associated IL-8 (A) and MCP-1 (B). HRPE cells (HRPE), monocytes (Mo), and HRPE cell/monocyte co-cultures were incubated with thrombin (10 U/ml) for 4 hours. HRPE cells and monocytes in the co-cultures were separated, and cells were lysed, as described in Materials and Methods. IL-8 and MCP-1 levels were measured by ELISA. c versus d, P < 0.05; a versus b, a versus e, e versus g, e versus f, f versus h, g versus h, i versus j, i versus m, m versus o, m versus n, and n versus p; P < 0.01 (n = 3).
Techniques Used: Incubation, Enzyme-linked Immunosorbent Assay
Figure Legend Snippet: Cell-cell contact enhanced thrombin induction of IL-8 (A), MCP-1 (B), and IL-6 (C) secretion by co-cultures. HRPE cells co-incubated with monocytes in the same cultures, but separated by porous polycarbonate filters (HRPE/Mo), and HRPE cells overlayed with monocytes directly (HRPE + Mo) were incubated with thrombin (10 U/ml). After 24 hours, supernatants were collected and IL-8, MCP-1, and IL-6 protein levels in supernatants were measured by ELISA. a versus c, b versus d, e versus g, f versus h, i versus k, and j versus l; P < 0.01 (n = 3).
Techniques Used: Incubation, Enzyme-linked Immunosorbent Assay
Figure Legend Snippet: Anti-TNF-α Ab, but not anti-IL-1β Ab, inhibited thrombin-induced IL-8 (A) and MCP-1 (B) secretion by HRPE cell/monocyte co-cultures. HRPE cell/monocyte co-cultures (HRPE + Mo) were incubated with anti-TNF-α Ab or anti-IL-1β Ab in the presence or absence of thrombin (10 U/ml) for 24 hours. Supernatants were collected and IL-8 and MCP-1 protein levels in supernatants were measured by ELISA (n = 3).
Techniques Used: Incubation, Enzyme-linked Immunosorbent Assay
Figure Legend Snippet: Effect of thrombin on rhIL-1β-induced (A and B) and rhTNF-α-induced (C and D) IL-8 (A and C), MCP-1 (B and D), and IL-6 (E) secretion. Thrombin had synergistic effects on rhIL-1β- and rhTNF-α-induced IL-8, MCP-1, and IL-6 secretion. HRPE cells (HRPE), monocytes (Mo), and HRPE cell/monocyte co-cultures (HRPE + Mo) were incubated in the medium containing rhIL-1β (0.2 ng/ml) or rhTNF-α (2 ng/ml), either alone or in combination with thrombin for 24 hours. Supernatants were collected and IL-8, MCP-1, and IL-6 protein levels in supernatants were measured by ELISA. *, P < 0.05; **, P < 0.01, compared with chemokine secretion from cells with rhIL-1β or rhTNF-α alone (n = 3).
Techniques Used: Incubation, Enzyme-linked Immunosorbent Assay