cell culture media hyq m199 ebss Search Results


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Corning Life Sciences medium 199
Medium 199, supplied by Corning Life Sciences, 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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ATCC atcc recommendations
Atcc Recommendations, supplied by ATCC, 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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Danaher Inc m199 medium
M199 Medium, supplied by Danaher Inc, 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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Corning Life Sciences m199
M199, supplied by Corning Life Sciences, 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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Thermo Fisher m199 medium
M199 Medium, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher earle s modified medium m199
Gel analysis of epitope-tagged ZP glycoproteins synthesized and secreted by growing mouse oocytes. Two hundred growing oocytes were isolated from 13-d-old mice, microinjected with Myc-mZP2, and cultured in <t>M199-M</t> for ∼5 h. Oocytes were then transferred to Met/Cys-depleted <t>M199-M,</t> supplemented with 4 mCi/ml [35S]Met/Cys. The culture medium was collected after ∼15 h and immunoprecipitated with monoclonal antibodies directed against Myc (9E10). Immunoprecipitates were subjected to 7.5% SDS-PAGE, as described in MATERIALS AND METHODS. Media from uninjected and injected oocytes probed with anti-Myc are shown in A and B, respectively. An arrowhead indicates the position of mZP2. Media were immunoprecipitated once again with an anti-mZP2 polyclonal antibody. As shown in C and D, both injected and noninjected oocytes secreted endogenous mZP2 glycoproteins. A band at ∼70 kDa was observed as a contaminant in all lanes. The positions of molecular mass standards are shown.
Earle S Modified Medium M199, 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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Thermo Fisher phenol red free m199
Gel analysis of epitope-tagged ZP glycoproteins synthesized and secreted by growing mouse oocytes. Two hundred growing oocytes were isolated from 13-d-old mice, microinjected with Myc-mZP2, and cultured in <t>M199-M</t> for ∼5 h. Oocytes were then transferred to Met/Cys-depleted <t>M199-M,</t> supplemented with 4 mCi/ml [35S]Met/Cys. The culture medium was collected after ∼15 h and immunoprecipitated with monoclonal antibodies directed against Myc (9E10). Immunoprecipitates were subjected to 7.5% SDS-PAGE, as described in MATERIALS AND METHODS. Media from uninjected and injected oocytes probed with anti-Myc are shown in A and B, respectively. An arrowhead indicates the position of mZP2. Media were immunoprecipitated once again with an anti-mZP2 polyclonal antibody. As shown in C and D, both injected and noninjected oocytes secreted endogenous mZP2 glycoproteins. A band at ∼70 kDa was observed as a contaminant in all lanes. The positions of molecular mass standards are shown.
Phenol Red Free M199, 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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InnoPharma inc m199 medium innopharma screen
Gel analysis of epitope-tagged ZP glycoproteins synthesized and secreted by growing mouse oocytes. Two hundred growing oocytes were isolated from 13-d-old mice, microinjected with Myc-mZP2, and cultured in <t>M199-M</t> for ∼5 h. Oocytes were then transferred to Met/Cys-depleted <t>M199-M,</t> supplemented with 4 mCi/ml [35S]Met/Cys. The culture medium was collected after ∼15 h and immunoprecipitated with monoclonal antibodies directed against Myc (9E10). Immunoprecipitates were subjected to 7.5% SDS-PAGE, as described in MATERIALS AND METHODS. Media from uninjected and injected oocytes probed with anti-Myc are shown in A and B, respectively. An arrowhead indicates the position of mZP2. Media were immunoprecipitated once again with an anti-mZP2 polyclonal antibody. As shown in C and D, both injected and noninjected oocytes secreted endogenous mZP2 glycoproteins. A band at ∼70 kDa was observed as a contaminant in all lanes. The positions of molecular mass standards are shown.
M199 Medium Innopharma Screen, supplied by InnoPharma 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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Carl Roth GmbH m199
Gel analysis of epitope-tagged ZP glycoproteins synthesized and secreted by growing mouse oocytes. Two hundred growing oocytes were isolated from 13-d-old mice, microinjected with Myc-mZP2, and cultured in <t>M199-M</t> for ∼5 h. Oocytes were then transferred to Met/Cys-depleted <t>M199-M,</t> supplemented with 4 mCi/ml [35S]Met/Cys. The culture medium was collected after ∼15 h and immunoprecipitated with monoclonal antibodies directed against Myc (9E10). Immunoprecipitates were subjected to 7.5% SDS-PAGE, as described in MATERIALS AND METHODS. Media from uninjected and injected oocytes probed with anti-Myc are shown in A and B, respectively. An arrowhead indicates the position of mZP2. Media were immunoprecipitated once again with an anti-mZP2 polyclonal antibody. As shown in C and D, both injected and noninjected oocytes secreted endogenous mZP2 glycoproteins. A band at ∼70 kDa was observed as a contaminant in all lanes. The positions of molecular mass standards are shown.
M199, supplied by Carl Roth GmbH, 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/cell+culture+media+hyq+m199+ebss/phenol+red+free+m199+medium/pmc09418552-69-5-6
Average 90 stars, based on 1 article reviews
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Image Search Results


Gel analysis of epitope-tagged ZP glycoproteins synthesized and secreted by growing mouse oocytes. Two hundred growing oocytes were isolated from 13-d-old mice, microinjected with Myc-mZP2, and cultured in M199-M for ∼5 h. Oocytes were then transferred to Met/Cys-depleted M199-M, supplemented with 4 mCi/ml [35S]Met/Cys. The culture medium was collected after ∼15 h and immunoprecipitated with monoclonal antibodies directed against Myc (9E10). Immunoprecipitates were subjected to 7.5% SDS-PAGE, as described in MATERIALS AND METHODS. Media from uninjected and injected oocytes probed with anti-Myc are shown in A and B, respectively. An arrowhead indicates the position of mZP2. Media were immunoprecipitated once again with an anti-mZP2 polyclonal antibody. As shown in C and D, both injected and noninjected oocytes secreted endogenous mZP2 glycoproteins. A band at ∼70 kDa was observed as a contaminant in all lanes. The positions of molecular mass standards are shown.

Journal:

Article Title: Secretion and Assembly of Zona Pellucida Glycoproteins by Growing Mouse Oocytes Microinjected with Epitope-tagged cDNAs for mZP2 and mZP3 *

doi: 10.1091/mbc.01-09-0440

Figure Lengend Snippet: Gel analysis of epitope-tagged ZP glycoproteins synthesized and secreted by growing mouse oocytes. Two hundred growing oocytes were isolated from 13-d-old mice, microinjected with Myc-mZP2, and cultured in M199-M for ∼5 h. Oocytes were then transferred to Met/Cys-depleted M199-M, supplemented with 4 mCi/ml [35S]Met/Cys. The culture medium was collected after ∼15 h and immunoprecipitated with monoclonal antibodies directed against Myc (9E10). Immunoprecipitates were subjected to 7.5% SDS-PAGE, as described in MATERIALS AND METHODS. Media from uninjected and injected oocytes probed with anti-Myc are shown in A and B, respectively. An arrowhead indicates the position of mZP2. Media were immunoprecipitated once again with an anti-mZP2 polyclonal antibody. As shown in C and D, both injected and noninjected oocytes secreted endogenous mZP2 glycoproteins. A band at ∼70 kDa was observed as a contaminant in all lanes. The positions of molecular mass standards are shown.

Article Snippet: Growing oocytes (50 ± 10 μm in diameter; Sorensen and Wassarman, 1976 ; Eppig and Telfer, 1993 ; Eppig et al. , 1996 ) were released by puncturing ovaries with fine steel needles under a dissecting microscope in a culture dish containing prewarmed Earle's modified medium M199 (Invitrogen) supplemented with bovine serum albumin (BSA; 4 mg/ml) and sodium pyruvate (30 μg/ml; M199-M).

Techniques: Synthesized, Isolation, Cell Culture, Immunoprecipitation, SDS Page, Injection