Sex determination and milk protein genotyping of preimplantation stage bovine embryos using multiplex PCR
A method for determining the sex and milk protein genotypes (RFLPs) of preimplantation stage bovine embryos using multiplex polymerase chain reaction (PCR) is described. Day 6 to 7 embryos were micromanipulated to isolate 5 to 6 cells. These cells were then dried in reaction tubes for transport to t...
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Veröffentlicht in: | Theriogenology 1992-11, Vol.38 (5), p.969-978 |
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creator | Agrawala, P.L. Wagner, V.A. Geldermann, H. |
description | A method for determining the sex and milk protein genotypes (RFLPs) of preimplantation stage bovine embryos using multiplex polymerase chain reaction (PCR) is described. Day 6 to 7 embryos were micromanipulated to isolate 5 to 6 cells. These cells were then dried in reaction tubes for transport to the laboratory. Subsequently, two sets of PCRs were performed using Y chromosome, k-casein and β-lactoglobulin gene specific primers, followed by electrophoretic analysis of the PCR products. The presence or absence of the Y chromosome was ascertained in 90 of 92 embryos. Moreover, the k-casein specific fragment was amplified and detected in all these embryos. The PCR products were digested in order to genotype the k-casein gene. In 70% of the embryos, the β-lactoglobulin specific fragment was amplified, although together with some unspecific fragments. |
doi_str_mv | 10.1016/0093-691X(92)90171-M |
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Day 6 to 7 embryos were micromanipulated to isolate 5 to 6 cells. These cells were then dried in reaction tubes for transport to the laboratory. Subsequently, two sets of PCRs were performed using Y chromosome, k-casein and β-lactoglobulin gene specific primers, followed by electrophoretic analysis of the PCR products. The presence or absence of the Y chromosome was ascertained in 90 of 92 embryos. Moreover, the k-casein specific fragment was amplified and detected in all these embryos. The PCR products were digested in order to genotype the k-casein gene. 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Day 6 to 7 embryos were micromanipulated to isolate 5 to 6 cells. These cells were then dried in reaction tubes for transport to the laboratory. Subsequently, two sets of PCRs were performed using Y chromosome, k-casein and β-lactoglobulin gene specific primers, followed by electrophoretic analysis of the PCR products. The presence or absence of the Y chromosome was ascertained in 90 of 92 embryos. Moreover, the k-casein specific fragment was amplified and detected in all these embryos. The PCR products were digested in order to genotype the k-casein gene. In 70% of the embryos, the β-lactoglobulin specific fragment was amplified, although together with some unspecific fragments.</description><subject>bovine</subject><subject>embryo</subject><subject>genotyping</subject><subject>PCR</subject><subject>sexing</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNp9kE2P0zAQhi20iJbCP0Ar3xYOATtx7PqChCq-pK1AfEjcLMeeVF4SO2s7Ff33OLSCG6eRRs_MO_Mg9IySl5RQ_ooQ2VRc0h_PZf1CEipotX-A1nQrZNXUDb1C67_ICj1O6Y4Q0nBOH6EV5aIWVLZr5L7CL2whQxyd19kFj7W3eHTDTzzFkMF5fAAf8mly_oBDX7rgxmnQPp_xlPUBcBeOzgOGsYunkPCcFnqch-ymoSR83n15gh72ekjw9FI36Pu7t992H6rbT-8_7t7cVobVIldamF5aouW2bre8o6wD02sumGVC91a3LelBa2iNZnVXm9Y0wtqtpp0xlJeHN-jmvLecfz9Dymp0ycBQLoYwJyUaRglvGCskO5MmhpQi9GqKbtTxpChRi2O1CFSLQCVr9cex2pex60vA3I1g_w1dpBbg9RmA8ubRQVTJOPAGrItgsrLB_T_hN4Agjzg</recordid><startdate>19921101</startdate><enddate>19921101</enddate><creator>Agrawala, P.L.</creator><creator>Wagner, V.A.</creator><creator>Geldermann, H.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19921101</creationdate><title>Sex determination and milk protein genotyping of preimplantation stage bovine embryos using multiplex PCR</title><author>Agrawala, P.L. ; Wagner, V.A. ; Geldermann, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-a7cf9d0a982586b14becfa674d47afda550feaae5ca42b2c5c37dd8a1bcc16093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>bovine</topic><topic>embryo</topic><topic>genotyping</topic><topic>PCR</topic><topic>sexing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Agrawala, P.L.</creatorcontrib><creatorcontrib>Wagner, V.A.</creatorcontrib><creatorcontrib>Geldermann, H.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agrawala, P.L.</au><au>Wagner, V.A.</au><au>Geldermann, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex determination and milk protein genotyping of preimplantation stage bovine embryos using multiplex PCR</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>1992-11-01</date><risdate>1992</risdate><volume>38</volume><issue>5</issue><spage>969</spage><epage>978</epage><pages>969-978</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>A method for determining the sex and milk protein genotypes (RFLPs) of preimplantation stage bovine embryos using multiplex polymerase chain reaction (PCR) is described. Day 6 to 7 embryos were micromanipulated to isolate 5 to 6 cells. These cells were then dried in reaction tubes for transport to the laboratory. Subsequently, two sets of PCRs were performed using Y chromosome, k-casein and β-lactoglobulin gene specific primers, followed by electrophoretic analysis of the PCR products. The presence or absence of the Y chromosome was ascertained in 90 of 92 embryos. Moreover, the k-casein specific fragment was amplified and detected in all these embryos. The PCR products were digested in order to genotype the k-casein gene. In 70% of the embryos, the β-lactoglobulin specific fragment was amplified, although together with some unspecific fragments.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16727195</pmid><doi>10.1016/0093-691X(92)90171-M</doi><tpages>10</tpages></addata></record> |
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subjects | bovine embryo genotyping PCR sexing |
title | Sex determination and milk protein genotyping of preimplantation stage bovine embryos using multiplex PCR |
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