polyclonal rabbit anti-c- myc antibody Search Results


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Abbexa Ltd rabbit anti il 1β polyclonal
list of Specific markers used in the current study.
Rabbit Anti Il 1β Polyclonal, supplied by Abbexa Ltd, 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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Cusabio myc csb pa407491
list of Specific markers used in the current study.
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Cusabio rabbit polyclonal anti human lf antibodies csb pa00870eorb
NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
Rabbit Polyclonal Anti Human Lf Antibodies Csb Pa00870eorb, supplied by Cusabio, 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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OriGene myc antibody
NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
Myc Antibody, supplied by OriGene, 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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NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
Mycn, supplied by OriGene, 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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Gramsch Inc rabbit anti-myc antibodies
NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
Rabbit Anti Myc Antibodies, supplied by Gramsch 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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Becton Dickinson rabbit polyclonal antibody c-myc
NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
Rabbit Polyclonal Antibody C Myc, 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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Oncogene Science Inc antic-fos rabbit polyclonal antibody ab-5
NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
Antic Fos Rabbit Polyclonal Antibody Ab 5, supplied by Oncogene Science 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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GeNOsys Inc pan-myc, mouse monoclonal antibody
NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf <t>(CSB-PA00870EORb)</t> or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.
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Image Search Results


list of Specific markers used in the current study.

Journal: Scientific Reports

Article Title: Panton–Valentine Leukocidin Colocalizes with Retinal Ganglion and Amacrine Cells and Activates Glial Reactions and Microglial Apoptosis

doi: 10.1038/s41598-018-20590-z

Figure Lengend Snippet: list of Specific markers used in the current study.

Article Snippet: IL-1β , Rabbit anti-IL-1β polyclonal , Abbexa Ltd, Cambridge, UK , 1:2000.

Techniques: Concentration Assay, TUNEL Assay

NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf (CSB-PA00870EORb) or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.

Journal: Frontiers in Immunology

Article Title: The Presence of Anti-Lactoferrin Antibodies in a Subgroup of Eosinophilic Granulomatosis with Polyangiitis Patients and Their Possible Contribution to Enhancement of Neutrophil Extracellular Trap Formation

doi: 10.3389/fimmu.2016.00636

Figure Lengend Snippet: NET induction assay . Peripheral blood neutrophils obtained from healthy volunteers were seeded on chamber slides (1 × 10 5 /mL), incubated for 15 min at 37°C, and then exposed to 0 or 10 nM phorbol myristate acetate (PMA) combined with 1 µg/mL aLf (CSB-PA00870EORb) or control rabbit IgG. After incubation for 3 h at 37°C, the samples were fixed with 4% paraformaldehyde followed by mounting with a solution containing DAPI. For positive control, the neutrophils were exposed to 100 nM PMA for 3 h at 37°C. (A) The representative photomicrographs are shown (original magnification: ×200). (B) NET area was represented by DAPI-positive area, which was calculated using Image J software. Data were presented as mean ± SD values of relative NET induction in which the value of the positive control (PMA 100 nM) was set as 1. Experiments were repeated five times. ** p < 0.01.

Article Snippet: For in vitro assay, rabbit polyclonal anti-human Lf antibodies (CSB-PA00870EORb) (Cusabio Biotech, Hubei, China) and rabbit control IgG (Beckman Coulter, Tokyo, Japan) were employed.

Techniques: Incubation, Control, Positive Control, Software