Primer, probe, composition and method for screening and identifying MLL rearrangement correlated fusion genes by utilizing multi-fluorescent polymerase chain reaction (PCR) technology

The invention relates to a primer, a probe, a composition and a method for screening and identifying MLL rearrangement correlated fusion genes by utilizing a multi-fluorescent polymerase chain reaction (PCR) technology. The screened MLL rearrangement correlated fusion genes comprise thirteen relativ...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: ZOU YUAN, CHEN HONGMEI, DU CUI, XIA CHENGQING
Format: Patent
Sprache:chi ; eng
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 ZOU YUAN
CHEN HONGMEI
DU CUI
XIA CHENGQING
description The invention relates to a primer, a probe, a composition and a method for screening and identifying MLL rearrangement correlated fusion genes by utilizing a multi-fluorescent polymerase chain reaction (PCR) technology. The screened MLL rearrangement correlated fusion genes comprise thirteen relatively common fusion genes, i.e., MLL-AF9, MLL-AF6, MLL-AF4, MLL-AF1P, MLL-AF1Q, MLL-AF10, MLL-AF17, MLL-AFX1, MLL-ELL, MLL-ENL, MLL-SEPT6, MLL-CBP and dup MLL. The primer, the probe, the testing combination way and the detection method are convenient, economical, fast, good in specificity, high in sensitivity and large in flux, thus being suitable for clinical test of large-batch samples. 本发明种用多重荧光PCR技术筛查MLL重排相关融合基因的引物、探针、组合物和方法。所述筛查的MLL重排相关融合基因包括:MLL-AF9、MLL-AF6、MLL-AF4、MLL-AF1P、MLL-AF1Q、MLL-AF10、MLL-AF17、MLL-AFX1、MLL-ELL、MLL-ENL、MLL-SEPT6、MLL-CBP、dupMLL共计13种相对常见融合基因。本发明所述引物、探针、检测组合方式和检测方法方便、经济、快捷,特异性好,灵敏度高,通量大,适于大批量样本的临床检测。
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN105969866A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN105969866A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN105969866A3</originalsourceid><addsrcrecordid>eNqNjsFKAzEQhvfiQarvMN4UWlDExR7LonioUsR7SbP_7g4kmTDJHtYX8_VMig_gaZj55_v4L5ufg7KHrimqnLAmKz5K4swSyISePPIkPQ2ilKwCgcN4DrhHyDwsdX_f70lhVE0Y4cu9aFThTEZB51RlIwISnRaaMzv-rpifXebN4GZRJFuxKG4pbUwC2clwqFZ77nJ76D7vKMNOQZyMy1VzMRiXcP03V83N68tX97ZBlCNSNMWHfOw-Hu6ftu32uW13j__5-QVDCl5d</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Primer, probe, composition and method for screening and identifying MLL rearrangement correlated fusion genes by utilizing multi-fluorescent polymerase chain reaction (PCR) technology</title><source>esp@cenet</source><creator>ZOU YUAN ; CHEN HONGMEI ; DU CUI ; XIA CHENGQING</creator><creatorcontrib>ZOU YUAN ; CHEN HONGMEI ; DU CUI ; XIA CHENGQING</creatorcontrib><description>The invention relates to a primer, a probe, a composition and a method for screening and identifying MLL rearrangement correlated fusion genes by utilizing a multi-fluorescent polymerase chain reaction (PCR) technology. The screened MLL rearrangement correlated fusion genes comprise thirteen relatively common fusion genes, i.e., MLL-AF9, MLL-AF6, MLL-AF4, MLL-AF1P, MLL-AF1Q, MLL-AF10, MLL-AF17, MLL-AFX1, MLL-ELL, MLL-ENL, MLL-SEPT6, MLL-CBP and dup MLL. The primer, the probe, the testing combination way and the detection method are convenient, economical, fast, good in specificity, high in sensitivity and large in flux, thus being suitable for clinical test of large-batch samples. 本发明种用多重荧光PCR技术筛查MLL重排相关融合基因的引物、探针、组合物和方法。所述筛查的MLL重排相关融合基因包括:MLL-AF9、MLL-AF6、MLL-AF4、MLL-AF1P、MLL-AF1Q、MLL-AF10、MLL-AF17、MLL-AFX1、MLL-ELL、MLL-ENL、MLL-SEPT6、MLL-CBP、dupMLL共计13种相对常见融合基因。本发明所述引物、探针、检测组合方式和检测方法方便、经济、快捷,特异性好,灵敏度高,通量大,适于大批量样本的临床检测。</description><language>chi ; eng</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS OR TEST PAPERS THEREFOR ; COMPOSITIONS THEREOF ; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES ; CULTURE MEDIA ; ENZYMOLOGY ; MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; PROCESSES OF PREPARING SUCH COMPOSITIONS ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2016</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&amp;date=20160928&amp;DB=EPODOC&amp;CC=CN&amp;NR=105969866A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20160928&amp;DB=EPODOC&amp;CC=CN&amp;NR=105969866A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>ZOU YUAN</creatorcontrib><creatorcontrib>CHEN HONGMEI</creatorcontrib><creatorcontrib>DU CUI</creatorcontrib><creatorcontrib>XIA CHENGQING</creatorcontrib><title>Primer, probe, composition and method for screening and identifying MLL rearrangement correlated fusion genes by utilizing multi-fluorescent polymerase chain reaction (PCR) technology</title><description>The invention relates to a primer, a probe, a composition and a method for screening and identifying MLL rearrangement correlated fusion genes by utilizing a multi-fluorescent polymerase chain reaction (PCR) technology. The screened MLL rearrangement correlated fusion genes comprise thirteen relatively common fusion genes, i.e., MLL-AF9, MLL-AF6, MLL-AF4, MLL-AF1P, MLL-AF1Q, MLL-AF10, MLL-AF17, MLL-AFX1, MLL-ELL, MLL-ENL, MLL-SEPT6, MLL-CBP and dup MLL. The primer, the probe, the testing combination way and the detection method are convenient, economical, fast, good in specificity, high in sensitivity and large in flux, thus being suitable for clinical test of large-batch samples. 本发明种用多重荧光PCR技术筛查MLL重排相关融合基因的引物、探针、组合物和方法。所述筛查的MLL重排相关融合基因包括:MLL-AF9、MLL-AF6、MLL-AF4、MLL-AF1P、MLL-AF1Q、MLL-AF10、MLL-AF17、MLL-AFX1、MLL-ELL、MLL-ENL、MLL-SEPT6、MLL-CBP、dupMLL共计13种相对常见融合基因。本发明所述引物、探针、检测组合方式和检测方法方便、经济、快捷,特异性好,灵敏度高,通量大,适于大批量样本的临床检测。</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS OR TEST PAPERS THEREFOR</subject><subject>COMPOSITIONS THEREOF</subject><subject>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>PROCESSES OF PREPARING SUCH COMPOSITIONS</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2016</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjsFKAzEQhvfiQarvMN4UWlDExR7LonioUsR7SbP_7g4kmTDJHtYX8_VMig_gaZj55_v4L5ufg7KHrimqnLAmKz5K4swSyISePPIkPQ2ilKwCgcN4DrhHyDwsdX_f70lhVE0Y4cu9aFThTEZB51RlIwISnRaaMzv-rpifXebN4GZRJFuxKG4pbUwC2clwqFZ77nJ76D7vKMNOQZyMy1VzMRiXcP03V83N68tX97ZBlCNSNMWHfOw-Hu6ftu32uW13j__5-QVDCl5d</recordid><startdate>20160928</startdate><enddate>20160928</enddate><creator>ZOU YUAN</creator><creator>CHEN HONGMEI</creator><creator>DU CUI</creator><creator>XIA CHENGQING</creator><scope>EVB</scope></search><sort><creationdate>20160928</creationdate><title>Primer, probe, composition and method for screening and identifying MLL rearrangement correlated fusion genes by utilizing multi-fluorescent polymerase chain reaction (PCR) technology</title><author>ZOU YUAN ; CHEN HONGMEI ; DU CUI ; XIA CHENGQING</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN105969866A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2016</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS OR TEST PAPERS THEREFOR</topic><topic>COMPOSITIONS THEREOF</topic><topic>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>PROCESSES OF PREPARING SUCH COMPOSITIONS</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>ZOU YUAN</creatorcontrib><creatorcontrib>CHEN HONGMEI</creatorcontrib><creatorcontrib>DU CUI</creatorcontrib><creatorcontrib>XIA CHENGQING</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>ZOU YUAN</au><au>CHEN HONGMEI</au><au>DU CUI</au><au>XIA CHENGQING</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Primer, probe, composition and method for screening and identifying MLL rearrangement correlated fusion genes by utilizing multi-fluorescent polymerase chain reaction (PCR) technology</title><date>2016-09-28</date><risdate>2016</risdate><abstract>The invention relates to a primer, a probe, a composition and a method for screening and identifying MLL rearrangement correlated fusion genes by utilizing a multi-fluorescent polymerase chain reaction (PCR) technology. The screened MLL rearrangement correlated fusion genes comprise thirteen relatively common fusion genes, i.e., MLL-AF9, MLL-AF6, MLL-AF4, MLL-AF1P, MLL-AF1Q, MLL-AF10, MLL-AF17, MLL-AFX1, MLL-ELL, MLL-ENL, MLL-SEPT6, MLL-CBP and dup MLL. The primer, the probe, the testing combination way and the detection method are convenient, economical, fast, good in specificity, high in sensitivity and large in flux, thus being suitable for clinical test of large-batch samples. 本发明种用多重荧光PCR技术筛查MLL重排相关融合基因的引物、探针、组合物和方法。所述筛查的MLL重排相关融合基因包括:MLL-AF9、MLL-AF6、MLL-AF4、MLL-AF1P、MLL-AF1Q、MLL-AF10、MLL-AF17、MLL-AFX1、MLL-ELL、MLL-ENL、MLL-SEPT6、MLL-CBP、dupMLL共计13种相对常见融合基因。本发明所述引物、探针、检测组合方式和检测方法方便、经济、快捷,特异性好,灵敏度高,通量大,适于大批量样本的临床检测。</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language chi ; eng
recordid cdi_epo_espacenet_CN105969866A
source esp@cenet
subjects BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS OR TEST PAPERS THEREFOR
COMPOSITIONS THEREOF
CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES
CULTURE MEDIA
ENZYMOLOGY
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS
METALLURGY
MICROBIOLOGY
MICROORGANISMS OR ENZYMES
MUTATION OR GENETIC ENGINEERING
PROCESSES OF PREPARING SUCH COMPOSITIONS
PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS
SPIRITS
VINEGAR
WINE
title Primer, probe, composition and method for screening and identifying MLL rearrangement correlated fusion genes by utilizing multi-fluorescent polymerase chain reaction (PCR) technology
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T04%3A28%3A28IST&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=ZOU%20YUAN&rft.date=2016-09-28&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN105969866A%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