DNA amplification fingerprintings of breast cancer cell (MCF-7) and human mammary epithelial cell (MCF-10A)
Copyright information:Taken from "Evidence of a Genomic Biomarker in Normal Human Epithelial Mammary Cell Line, MCF-10A, That Is Absent in the Human Breast Cancer Cell Line, MCF-7"Journal of Biomedicine and Biotechnology 2006;2006():-.Published online Jan 2006PMCID:PMC1510942. Three μL of...
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creator | Crawford, Brian H. AKM A. Hussain Jideama, Nathan M. |
description | Copyright information:Taken from "Evidence of a Genomic Biomarker in Normal Human Epithelial Mammary Cell Line, MCF-10A, That Is Absent in the Human Breast Cancer Cell Line, MCF-7"Journal of Biomedicine and Biotechnology 2006;2006():-.Published online Jan 2006PMCID:PMC1510942. Three μL of the DAF PCR amplification reaction mixture was loaded with 3 μL of loading buffer. Electrophoresis was continued at 100 V until the dye front was approximately 1 cm from the end of the gel. The amplification fragments were separated by polyacrylamide gel (5%) electrophoresis. DNA was visualized using a fast and sensitive silver staining procedure that detects 1 pg DNA/mm band cross-section. The polymorphic marker was found at 262 bps. These results were confirmed by three additional experiments. |
doi_str_mv | 10.6084/m9.figshare.40607 |
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Hussain ; Jideama, Nathan M.</creatorcontrib><description>Copyright information:Taken from "Evidence of a Genomic Biomarker in Normal Human Epithelial Mammary Cell Line, MCF-10A, That Is Absent in the Human Breast Cancer Cell Line, MCF-7"Journal of Biomedicine and Biotechnology 2006;2006():-.Published online Jan 2006PMCID:PMC1510942. Three μL of the DAF PCR amplification reaction mixture was loaded with 3 μL of loading buffer. Electrophoresis was continued at 100 V until the dye front was approximately 1 cm from the end of the gel. The amplification fragments were separated by polyacrylamide gel (5%) electrophoresis. DNA was visualized using a fast and sensitive silver staining procedure that detects 1 pg DNA/mm band cross-section. The polymorphic marker was found at 262 bps. These results were confirmed by three additional experiments.</description><identifier>DOI: 10.6084/m9.figshare.40607</identifier><language>eng</language><publisher>figshare</publisher><subject>Molecular Biology</subject><creationdate>2011</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>777,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.40607$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Crawford, Brian H.</creatorcontrib><creatorcontrib>AKM A. Hussain</creatorcontrib><creatorcontrib>Jideama, Nathan M.</creatorcontrib><title>DNA amplification fingerprintings of breast cancer cell (MCF-7) and human mammary epithelial cell (MCF-10A)</title><description>Copyright information:Taken from "Evidence of a Genomic Biomarker in Normal Human Epithelial Mammary Cell Line, MCF-10A, That Is Absent in the Human Breast Cancer Cell Line, MCF-7"Journal of Biomedicine and Biotechnology 2006;2006():-.Published online Jan 2006PMCID:PMC1510942. Three μL of the DAF PCR amplification reaction mixture was loaded with 3 μL of loading buffer. Electrophoresis was continued at 100 V until the dye front was approximately 1 cm from the end of the gel. The amplification fragments were separated by polyacrylamide gel (5%) electrophoresis. DNA was visualized using a fast and sensitive silver staining procedure that detects 1 pg DNA/mm band cross-section. The polymorphic marker was found at 262 bps. These results were confirmed by three additional experiments.</description><subject>Molecular Biology</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2011</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNqdjisPwjAUhWsQBPgBuCuZ2OgCYUwSYMGAwjeXcstuaLulK4J_zyOQoFHniPP4hBjnMlvI5XzqyszwpasxUDaXC1n0xXVzWAG61rJhjZEbD4b9hUIb2Men66AxcAqEXQSNXlMATdbCZL-u0iIB9Geobw49OHQOwx2o5ViTZbQ_yVyukqHoGbQdjT46EHm1Pa536Rkjao6knqevCZVL9QJWrlRfYPUGnv3TeQAkYFH_</recordid><startdate>20111231</startdate><enddate>20111231</enddate><creator>Crawford, Brian H.</creator><creator>AKM A. Hussain</creator><creator>Jideama, Nathan M.</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20111231</creationdate><title>DNA amplification fingerprintings of breast cancer cell (MCF-7) and human mammary epithelial cell (MCF-10A)</title><author>Crawford, Brian H. ; AKM A. Hussain ; Jideama, Nathan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_406073</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Molecular Biology</topic><toplevel>online_resources</toplevel><creatorcontrib>Crawford, Brian H.</creatorcontrib><creatorcontrib>AKM A. Hussain</creatorcontrib><creatorcontrib>Jideama, Nathan M.</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Crawford, Brian H.</au><au>AKM A. Hussain</au><au>Jideama, Nathan M.</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>DNA amplification fingerprintings of breast cancer cell (MCF-7) and human mammary epithelial cell (MCF-10A)</title><date>2011-12-31</date><risdate>2011</risdate><abstract>Copyright information:Taken from "Evidence of a Genomic Biomarker in Normal Human Epithelial Mammary Cell Line, MCF-10A, That Is Absent in the Human Breast Cancer Cell Line, MCF-7"Journal of Biomedicine and Biotechnology 2006;2006():-.Published online Jan 2006PMCID:PMC1510942. Three μL of the DAF PCR amplification reaction mixture was loaded with 3 μL of loading buffer. Electrophoresis was continued at 100 V until the dye front was approximately 1 cm from the end of the gel. The amplification fragments were separated by polyacrylamide gel (5%) electrophoresis. DNA was visualized using a fast and sensitive silver staining procedure that detects 1 pg DNA/mm band cross-section. 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title | DNA amplification fingerprintings of breast cancer cell (MCF-7) and human mammary epithelial cell (MCF-10A) |
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