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mvac (measles virus live i. p)  (Serum Institute India)

 
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    Serum Institute India mvac (measles virus live i. p)
    Mvac (Measles Virus Live I. P), supplied by Serum Institute India, 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/mvac/measles+vaccine+m+vac/us11535864-323-0-8
    Average 90 stars, based on 1 article reviews
    mvac (measles virus live i. p) - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Immunopeptidomics:

    Article Title: Multicenter Safety and Immunogenicity Trial of an Attenuated Measles Vaccine for NHP
    Article Snippet: .. This need for a readily available vaccine led us to perform a broad, multicenter safety and immunogenicity study of another candidate vaccine, MVac (Serum Institute of India), a monovalent measles vaccine derived from live Edmonston–Zagreb strain virus that had been attenuated after 22 passages on human diploid cells. ..

    Derivative Assay:

    Article Title: Multicenter Safety and Immunogenicity Trial of an Attenuated Measles Vaccine for NHP
    Article Snippet: .. This need for a readily available vaccine led us to perform a broad, multicenter safety and immunogenicity study of another candidate vaccine, MVac (Serum Institute of India), a monovalent measles vaccine derived from live Edmonston–Zagreb strain virus that had been attenuated after 22 passages on human diploid cells. ..

    Virus:

    Article Title: Multicenter Safety and Immunogenicity Trial of an Attenuated Measles Vaccine for NHP
    Article Snippet: .. This need for a readily available vaccine led us to perform a broad, multicenter safety and immunogenicity study of another candidate vaccine, MVac (Serum Institute of India), a monovalent measles vaccine derived from live Edmonston–Zagreb strain virus that had been attenuated after 22 passages on human diploid cells. ..

    Produced:

    Article Title: Multicenter Safety and Immunogenicity Trial of an Attenuated Measles Vaccine for NHP
    Article Snippet: .. Given the lack of a viable, domestic-source, monovalent measles vaccine and alternatives, a collaborative effort was established among the United States NIH P51-supported National Primate Research Centers to investigate the safety and efficacy of MVac, a live attenuated measles vaccine that is licensed by the World Health Organization for use in humans and produced by the Serum Institute of India. ..



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    In vitro development of fresh bovine IVM oocytes (fresh control), bovine IVM oocytes treated with vitrification solution (solution control) and bovine IVM oocytes vitrified using the MVAC or Cryotop device after IVF and in vitro culture for 9 days

    Journal: The Journal of Reproduction and Development

    Article Title: Comparison of Cryotop and micro volume air cooling methods for cryopreservation of bovine matured oocytes and blastocysts

    doi: 10.1262/jrd.2014-163

    Figure Lengend Snippet: In vitro development of fresh bovine IVM oocytes (fresh control), bovine IVM oocytes treated with vitrification solution (solution control) and bovine IVM oocytes vitrified using the MVAC or Cryotop device after IVF and in vitro culture for 9 days

    Article Snippet: Thereafter, they were vitrified using either the MVAC device or the Cryotop device (Kitazato BioPharma, Shizuoka, Japan) in a vitrification solution, as described previously by Dinnyes et al . [ ].

    Techniques: In Vitro

    Cell numbers in blastocysts derived from fresh bovine IVM oocytes (fresh control), bovine IVM oocytes treated with vitrification solution (solution control) or bovine IVM oocytes vitrified by the MVAC or Cryotop methods after IVF and in vitro culture for 9 days. Data presented as the mean no. of nuclei ± SEM. Fresh control: IVM oocytes without any vitrification treatments. Solution control: IVM oocytes that were exposed to vitrification and warming solutions. MVAC: IVM oocytes that were vitrified by inserting the MVAC device containing them into a precooled 0.25-ml plastic straw. MVAC in LN 2 : IVM oocytes that were vitrified by plunging the MVAC device containing them directly into LN 2 . Cryotop: IVM oocytes that were vitrified by the Cryotop method. ICM: inner cell mass. TE: trophectoderm. No significant differences in ICM and TE cell numbers were detected between the treatment groups at P < 0.05 using one-way ANOVA.

    Journal: The Journal of Reproduction and Development

    Article Title: Comparison of Cryotop and micro volume air cooling methods for cryopreservation of bovine matured oocytes and blastocysts

    doi: 10.1262/jrd.2014-163

    Figure Lengend Snippet: Cell numbers in blastocysts derived from fresh bovine IVM oocytes (fresh control), bovine IVM oocytes treated with vitrification solution (solution control) or bovine IVM oocytes vitrified by the MVAC or Cryotop methods after IVF and in vitro culture for 9 days. Data presented as the mean no. of nuclei ± SEM. Fresh control: IVM oocytes without any vitrification treatments. Solution control: IVM oocytes that were exposed to vitrification and warming solutions. MVAC: IVM oocytes that were vitrified by inserting the MVAC device containing them into a precooled 0.25-ml plastic straw. MVAC in LN 2 : IVM oocytes that were vitrified by plunging the MVAC device containing them directly into LN 2 . Cryotop: IVM oocytes that were vitrified by the Cryotop method. ICM: inner cell mass. TE: trophectoderm. No significant differences in ICM and TE cell numbers were detected between the treatment groups at P < 0.05 using one-way ANOVA.

    Article Snippet: Thereafter, they were vitrified using either the MVAC device or the Cryotop device (Kitazato BioPharma, Shizuoka, Japan) in a vitrification solution, as described previously by Dinnyes et al . [ ].

    Techniques: Derivative Assay, In Vitro

    Development to the hatched blastocyst stage of in vitro -produced expanded blastocysts vitrified using the MVAC or Cryotop device, warmed and cultured in vitro for 72 h

    Journal: The Journal of Reproduction and Development

    Article Title: Comparison of Cryotop and micro volume air cooling methods for cryopreservation of bovine matured oocytes and blastocysts

    doi: 10.1262/jrd.2014-163

    Figure Lengend Snippet: Development to the hatched blastocyst stage of in vitro -produced expanded blastocysts vitrified using the MVAC or Cryotop device, warmed and cultured in vitro for 72 h

    Article Snippet: Thereafter, they were vitrified using either the MVAC device or the Cryotop device (Kitazato BioPharma, Shizuoka, Japan) in a vitrification solution, as described previously by Dinnyes et al . [ ].

    Techniques: In Vitro, Produced, Cell Culture