ESTABLISHMENT OF A HUMAN EMBRYONIC STEM CELL LINE USING MAMMALIAN CELLS
Purified preparations of human embryonic stem cells with certain population- specific characteristics are disclosed. This preparation is characterized by the positive expression of the following pluripotent cell surface markers: SSEA-1 (-); SSEA-4 (+); TRA-1-60 (+); TRA-1-81 (+); alkaline phosphatas...
Gespeichert in:
Hauptverfasser: | , , , , , , , , |
---|---|
Format: | Patent |
Sprache: | eng ; fre |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | BIPASHA, BOSE TIPNIS, SHABARI ALAM, KHAN FIRDOS JAYANT, KULKAMI RAJARSHI, PAL GEETA, RAVINDRAN ARUNDHATI, MANDAL ARNEET, PATKI APARNA, KHANNA |
description | Purified preparations of human embryonic stem cells with certain population- specific characteristics are disclosed. This preparation is characterized by the positive expression of the following pluripotent cell surface markers: SSEA-1 (-); SSEA-4 (+); TRA-1-60 (+); TRA-1-81 (+); alkaline phosphatase (+) , as well as a set of ES cell markers including Oct-4, Nanog, Rexl, Sox2, Thyl , FGF4, ABCG2, Dppa5, UTFl, Criptol, hTERT, Connexin-43 and Connexin-45. The cells of the preparation are negative for lineage specific markers like Keratin 8, Sox-1, NFH (ectoderm), MyoD, brachyury, cardiac-actin (mesoderm), HNF-3 beta, albumin, and PDXl (endoderm). The cells of the preparation are human embryonic stem cells, have normal karyotypes, exhibit high telomerase activity and continue to proliferate in an undifferentiated state after continuous culture for over 40 passages. The embryonic stem cell line RelicellTM Hes1 also retains the ability, throughout the culture, to differentiate into cell and tissue types derived from all three embryonic ge rm layers (endoderm, mesoderm and ectoderm). Methods for isolating a human embryonic stem cell line are also disclosed. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CA2608833A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CA2608833A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CA2608833A13</originalsourceid><addsrcrecordid>eNrjZHB3DQ5xdPLxDPbwdfULUfB3U3BU8Aj1dfRTcPV1Cor09_N0VggOcfVVcHb18VHw8fRzVQgN9vRzV_B19PV19PEEKgTJBPMwsKYl5hSn8kJpbgYFN9cQZw_d1IL8-NTigsTk1LzUknhnRyMzAwsLY2NHQ2MilAAAXeQrwQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>ESTABLISHMENT OF A HUMAN EMBRYONIC STEM CELL LINE USING MAMMALIAN CELLS</title><source>esp@cenet</source><creator>BIPASHA, BOSE ; TIPNIS, SHABARI ; ALAM, KHAN FIRDOS ; JAYANT, KULKAMI ; RAJARSHI, PAL ; GEETA, RAVINDRAN ; ARUNDHATI, MANDAL ; ARNEET, PATKI ; APARNA, KHANNA</creator><creatorcontrib>BIPASHA, BOSE ; TIPNIS, SHABARI ; ALAM, KHAN FIRDOS ; JAYANT, KULKAMI ; RAJARSHI, PAL ; GEETA, RAVINDRAN ; ARUNDHATI, MANDAL ; ARNEET, PATKI ; APARNA, KHANNA</creatorcontrib><description>Purified preparations of human embryonic stem cells with certain population- specific characteristics are disclosed. This preparation is characterized by the positive expression of the following pluripotent cell surface markers: SSEA-1 (-); SSEA-4 (+); TRA-1-60 (+); TRA-1-81 (+); alkaline phosphatase (+) , as well as a set of ES cell markers including Oct-4, Nanog, Rexl, Sox2, Thyl , FGF4, ABCG2, Dppa5, UTFl, Criptol, hTERT, Connexin-43 and Connexin-45. The cells of the preparation are negative for lineage specific markers like Keratin 8, Sox-1, NFH (ectoderm), MyoD, brachyury, cardiac-actin (mesoderm), HNF-3 beta, albumin, and PDXl (endoderm). The cells of the preparation are human embryonic stem cells, have normal karyotypes, exhibit high telomerase activity and continue to proliferate in an undifferentiated state after continuous culture for over 40 passages. The embryonic stem cell line RelicellTM Hes1 also retains the ability, throughout the culture, to differentiate into cell and tissue types derived from all three embryonic ge rm layers (endoderm, mesoderm and ectoderm). Methods for isolating a human embryonic stem cell line are also disclosed.</description><language>eng ; fre</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS THEREOF ; CULTURE MEDIA ; ENZYMOLOGY ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2007</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20070222&DB=EPODOC&CC=CA&NR=2608833A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25562,76317</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20070222&DB=EPODOC&CC=CA&NR=2608833A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BIPASHA, BOSE</creatorcontrib><creatorcontrib>TIPNIS, SHABARI</creatorcontrib><creatorcontrib>ALAM, KHAN FIRDOS</creatorcontrib><creatorcontrib>JAYANT, KULKAMI</creatorcontrib><creatorcontrib>RAJARSHI, PAL</creatorcontrib><creatorcontrib>GEETA, RAVINDRAN</creatorcontrib><creatorcontrib>ARUNDHATI, MANDAL</creatorcontrib><creatorcontrib>ARNEET, PATKI</creatorcontrib><creatorcontrib>APARNA, KHANNA</creatorcontrib><title>ESTABLISHMENT OF A HUMAN EMBRYONIC STEM CELL LINE USING MAMMALIAN CELLS</title><description>Purified preparations of human embryonic stem cells with certain population- specific characteristics are disclosed. This preparation is characterized by the positive expression of the following pluripotent cell surface markers: SSEA-1 (-); SSEA-4 (+); TRA-1-60 (+); TRA-1-81 (+); alkaline phosphatase (+) , as well as a set of ES cell markers including Oct-4, Nanog, Rexl, Sox2, Thyl , FGF4, ABCG2, Dppa5, UTFl, Criptol, hTERT, Connexin-43 and Connexin-45. The cells of the preparation are negative for lineage specific markers like Keratin 8, Sox-1, NFH (ectoderm), MyoD, brachyury, cardiac-actin (mesoderm), HNF-3 beta, albumin, and PDXl (endoderm). The cells of the preparation are human embryonic stem cells, have normal karyotypes, exhibit high telomerase activity and continue to proliferate in an undifferentiated state after continuous culture for over 40 passages. The embryonic stem cell line RelicellTM Hes1 also retains the ability, throughout the culture, to differentiate into cell and tissue types derived from all three embryonic ge rm layers (endoderm, mesoderm and ectoderm). Methods for isolating a human embryonic stem cell line are also disclosed.</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS THEREOF</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2007</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZHB3DQ5xdPLxDPbwdfULUfB3U3BU8Aj1dfRTcPV1Cor09_N0VggOcfVVcHb18VHw8fRzVQgN9vRzV_B19PV19PEEKgTJBPMwsKYl5hSn8kJpbgYFN9cQZw_d1IL8-NTigsTk1LzUknhnRyMzAwsLY2NHQ2MilAAAXeQrwQ</recordid><startdate>20070222</startdate><enddate>20070222</enddate><creator>BIPASHA, BOSE</creator><creator>TIPNIS, SHABARI</creator><creator>ALAM, KHAN FIRDOS</creator><creator>JAYANT, KULKAMI</creator><creator>RAJARSHI, PAL</creator><creator>GEETA, RAVINDRAN</creator><creator>ARUNDHATI, MANDAL</creator><creator>ARNEET, PATKI</creator><creator>APARNA, KHANNA</creator><scope>EVB</scope></search><sort><creationdate>20070222</creationdate><title>ESTABLISHMENT OF A HUMAN EMBRYONIC STEM CELL LINE USING MAMMALIAN CELLS</title><author>BIPASHA, BOSE ; TIPNIS, SHABARI ; ALAM, KHAN FIRDOS ; JAYANT, KULKAMI ; RAJARSHI, PAL ; GEETA, RAVINDRAN ; ARUNDHATI, MANDAL ; ARNEET, PATKI ; APARNA, KHANNA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CA2608833A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2007</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>BIPASHA, BOSE</creatorcontrib><creatorcontrib>TIPNIS, SHABARI</creatorcontrib><creatorcontrib>ALAM, KHAN FIRDOS</creatorcontrib><creatorcontrib>JAYANT, KULKAMI</creatorcontrib><creatorcontrib>RAJARSHI, PAL</creatorcontrib><creatorcontrib>GEETA, RAVINDRAN</creatorcontrib><creatorcontrib>ARUNDHATI, MANDAL</creatorcontrib><creatorcontrib>ARNEET, PATKI</creatorcontrib><creatorcontrib>APARNA, KHANNA</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BIPASHA, BOSE</au><au>TIPNIS, SHABARI</au><au>ALAM, KHAN FIRDOS</au><au>JAYANT, KULKAMI</au><au>RAJARSHI, PAL</au><au>GEETA, RAVINDRAN</au><au>ARUNDHATI, MANDAL</au><au>ARNEET, PATKI</au><au>APARNA, KHANNA</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>ESTABLISHMENT OF A HUMAN EMBRYONIC STEM CELL LINE USING MAMMALIAN CELLS</title><date>2007-02-22</date><risdate>2007</risdate><abstract>Purified preparations of human embryonic stem cells with certain population- specific characteristics are disclosed. This preparation is characterized by the positive expression of the following pluripotent cell surface markers: SSEA-1 (-); SSEA-4 (+); TRA-1-60 (+); TRA-1-81 (+); alkaline phosphatase (+) , as well as a set of ES cell markers including Oct-4, Nanog, Rexl, Sox2, Thyl , FGF4, ABCG2, Dppa5, UTFl, Criptol, hTERT, Connexin-43 and Connexin-45. The cells of the preparation are negative for lineage specific markers like Keratin 8, Sox-1, NFH (ectoderm), MyoD, brachyury, cardiac-actin (mesoderm), HNF-3 beta, albumin, and PDXl (endoderm). The cells of the preparation are human embryonic stem cells, have normal karyotypes, exhibit high telomerase activity and continue to proliferate in an undifferentiated state after continuous culture for over 40 passages. The embryonic stem cell line RelicellTM Hes1 also retains the ability, throughout the culture, to differentiate into cell and tissue types derived from all three embryonic ge rm layers (endoderm, mesoderm and ectoderm). Methods for isolating a human embryonic stem cell line are also disclosed.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng ; fre |
recordid | cdi_epo_espacenet_CA2608833A1 |
source | esp@cenet |
subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA ENZYMOLOGY METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS VINEGAR WINE |
title | ESTABLISHMENT OF A HUMAN EMBRYONIC STEM CELL LINE USING MAMMALIAN CELLS |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T04%3A57%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=BIPASHA,%20BOSE&rft.date=2007-02-22&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECA2608833A1%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |