code for mie theory Search Results


vectorized mie-theory code (fastmie.m) in  (MathWorks Inc)
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MathWorks Inc vectorized mie-theory code (fastmie.m) in
Vectorized Mie Theory Code (Fastmie.M) In, supplied by MathWorks 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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mie theory matlab code  (MathWorks Inc)
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MathWorks Inc mie theory matlab code
Mie Theory Matlab Code, supplied by MathWorks 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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mab810 against hcmv major ie proteins  (Millipore)
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Millipore mab810 against hcmv major ie proteins
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Mab810 Against Hcmv Major Ie Proteins, supplied by Millipore, 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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mie  (Weksler)
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Weksler mie
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Mie, supplied by Weksler, 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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mie  (Bristol Myers)
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Bristol Myers mie
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Mie, supplied by Bristol Myers, 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/result/mie/product/Bristol Myers
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daikyo-cho, yokkaichi-shi, mie, japan  (Daikyo Seiko Ltd)
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Daikyo Seiko Ltd daikyo-cho, yokkaichi-shi, mie, japan
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Daikyo Cho, Yokkaichi Shi, Mie, Japan, supplied by Daikyo Seiko Ltd, 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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thermoresistivity  (EcoDesign Inc)
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EcoDesign Inc thermoresistivity
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Thermoresistivity, supplied by EcoDesign 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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clin. mie  (Verlag GmbH)
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Verlag GmbH clin. mie
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Clin. Mie, supplied by Verlag GmbH, 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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beitrage zur optik truber medien speziell kolloidaler metallosungen  (Optik GmbH)
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Optik GmbH beitrage zur optik truber medien speziell kolloidaler metallosungen
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Beitrage Zur Optik Truber Medien Speziell Kolloidaler Metallosungen, supplied by Optik GmbH, 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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tuneable coupling of surface plasmon-polaritons and mie plasmons  (Verlag GmbH)
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Verlag GmbH tuneable coupling of surface plasmon-polaritons and mie plasmons
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Tuneable Coupling Of Surface Plasmon Polaritons And Mie Plasmons, supplied by Verlag GmbH, 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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matlab-based implementation of mie theory  (MathWorks Inc)
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MathWorks Inc matlab-based implementation of mie theory
Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody <t>MAb810</t> (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.
Matlab Based Implementation Of Mie Theory, supplied by MathWorks 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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galbraith plot analysis  (Galbraith Laboratories Inc)
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Galbraith Laboratories Inc galbraith plot analysis
Galbraith plot of <t>MIE</t> <t>and</t> <t>pulmonary</t> complications
Galbraith Plot Analysis, supplied by Galbraith Laboratories 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


Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody MAb810 (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.

Journal:

Article Title: Functional Interaction between the pp71 Protein of Human Cytomegalovirus and the PML-Interacting Protein Human Daxx

doi: 10.1128/JVI.76.11.5769-5783.2002

Figure Lengend Snippet: Recruitment of pp71 after expression of FLAG-hDaxx. HFF cells (A) and HeLa cells (B) grown on coverslips were transfected with eukaryotic expression vectors encoding pp71-GFP, FLAG-hDaxx, and FLAG-Sp100, as well as the HCMV proteins ppUL69 and IE2, as indicated. Thereafter, indirect immunofluorescence analyses were carried out. pp71 was visible through its GFP moiety (panels Aa, d, k, and n; panels Ba and d). FLAG-hDaxx and FLAG-Sp100 were detected with the anti-FLAG monoclonal antibody (panels Ab and e; panel Be). ppUL69 was stained by using the polyclonal anti-UL69 antiserum (panels Ag and l); IE2 was detected with monoclonal antibody MAb810 (panel Ao). Staining for endogenous hDaxx was performed with a polyclonal anti-hDaxx antiserum (panel Bb). Thereafter, TRITC-conjugated anti-mouse secondary antibodies, as well as FITC-conjugated anti-rabbit secondary antibodies, were employed.

Article Snippet: The monoclonal antibody MAb810 against HCMV major IE proteins was obtained from Chemicon (Hofheim, Germany) ( 46 ).

Techniques: Expressing, Transfection, Immunofluorescence, Staining

Galbraith plot of MIE and pulmonary complications

Journal: World Journal of Surgical Oncology

Article Title: Minimally invasive oesophagectomy versus open esophagectomy for resectable esophageal cancer: a meta-analysis

doi: 10.1186/s12957-016-1062-7

Figure Lengend Snippet: Galbraith plot of MIE and pulmonary complications

Article Snippet: Fig. 3 Meta-analysis for MIE and pulmonary complications Fig. 4 Galbraith plot of MIE and pulmonary complications Fig. 5 Begg’s Test of MIE and pulmonary complications

Techniques:

Begg’s Test of MIE and pulmonary complications

Journal: World Journal of Surgical Oncology

Article Title: Minimally invasive oesophagectomy versus open esophagectomy for resectable esophageal cancer: a meta-analysis

doi: 10.1186/s12957-016-1062-7

Figure Lengend Snippet: Begg’s Test of MIE and pulmonary complications

Article Snippet: Fig. 3 Meta-analysis for MIE and pulmonary complications Fig. 4 Galbraith plot of MIE and pulmonary complications Fig. 5 Begg’s Test of MIE and pulmonary complications

Techniques:

The “trim and fill” method for MIE and pulmonary complications

Journal: World Journal of Surgical Oncology

Article Title: Minimally invasive oesophagectomy versus open esophagectomy for resectable esophageal cancer: a meta-analysis

doi: 10.1186/s12957-016-1062-7

Figure Lengend Snippet: The “trim and fill” method for MIE and pulmonary complications

Article Snippet: Fig. 3 Meta-analysis for MIE and pulmonary complications Fig. 4 Galbraith plot of MIE and pulmonary complications Fig. 5 Begg’s Test of MIE and pulmonary complications

Techniques:

The sensitivity analysis of MIE and pulmonary complications

Journal: World Journal of Surgical Oncology

Article Title: Minimally invasive oesophagectomy versus open esophagectomy for resectable esophageal cancer: a meta-analysis

doi: 10.1186/s12957-016-1062-7

Figure Lengend Snippet: The sensitivity analysis of MIE and pulmonary complications

Article Snippet: Fig. 3 Meta-analysis for MIE and pulmonary complications Fig. 4 Galbraith plot of MIE and pulmonary complications Fig. 5 Begg’s Test of MIE and pulmonary complications

Techniques: