pmel 1 tcr transgenic mice Search Results


86
Jackson Laboratory tcratcrb 8rest j commonly known as pmel 1 mice
Tcratcrb 8rest J Commonly Known As Pmel 1 Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory tcratcrb 8rest j pmel1 mice
Tcratcrb 8rest J Pmel1 Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Charles River Laboratories pmel 1 tcr thy1 1 pmel transgenic mice
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Jackson Laboratory mouse pmel 1
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Jackson Laboratory t cell receptor tcr transgenic thy1 1 pmel 1 pmel mice b6 cg thy1 a cytg tcrazcrb 8rest j
T Cell Receptor Tcr Transgenic Thy1 1 Pmel 1 Pmel Mice B6 Cg Thy1 A Cytg Tcrazcrb 8rest J, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory old female transgenic pmel 1 mouse
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Becton Dickinson anti-gr-1 (rb6-8c5 antibody
Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting <t>Gr-1</t> or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).
Anti Gr 1 (Rb6 8c5 Antibody, 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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Jackson Laboratory pmel
Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting <t>Gr-1</t> or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).
Pmel, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio X Cell anti ly6g
Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting <t>Gr-1</t> or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).
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Bio X Cell anti nk1 1
Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting <t>Gr-1</t> or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).
Anti Nk1 1, supplied by Bio X Cell, 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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Thermo Fisher newborn balb c mice
Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting <t>Gr-1</t> or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).
Newborn Balb C Mice, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting Gr-1 or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).

Journal: American Journal of Physiology - Lung Cellular and Molecular Physiology

Article Title: Moderate oxygen augments lipopolysaccharide-induced lung injury in mice

doi: 10.1152/ajplung.00308.2009

Figure Lengend Snippet: Neutrophil depletion abrogates the augmentation of LPS-induced lung injury by supplemental oxygen. Mice received LPS and supplemental oxygen as described, as well as concomitant treatment with neutrophil-depleting Gr-1 or isotype antibodies. Injury parameters were assessed at day 4. A: BAL neutrophils and macrophages were quantified (n = 3–5/group, *P < 0.05). B: representative lung histology sections from each group, stained with H&E. C: lung injury scores as described for each group; n = 3–5 mice/group; *P < 0.05. BAL protein and albumin (D) and wet lung to body weight (E) were in each group (n = 3–5/group, *P < 0.05). TNFα (F) and chemokines MIP-2 and KC (G) were assessed in BAL fluid of mice from each group (n = 3–5/group; *P < 0.05).

Article Snippet: Mice were administered intraperitoneal (IP) injections of anti-Gr-1 (RB6-8C5 clone) antibody [Ab; 250 μg·mouse −1 ·day −1 (BD Pharmingen, 553123) or isotype Ab (Rat IgG2b, κ) on day −2 and day 0 (at the time of LPS injection)].

Techniques: Staining