Culture medium and culture method of peritoneal malignant mesothelioma organoid

The invention discloses a culture medium and a culture method of peritoneal malignant mesothelioma organs. The culture medium comprises an initial culture medium and an amplification culture medium, wherein a formula of a second culture medium comprises Advanced DMEM/F12, 1-2% of P/S double antibodi...

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Hauptverfasser: CHEN TIANLIANG, SHU LIN, LI XUANFEI, FANG XIAOCHANG, FENG MAOHUI
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creator CHEN TIANLIANG
SHU LIN
LI XUANFEI
FANG XIAOCHANG
FENG MAOHUI
description The invention discloses a culture medium and a culture method of peritoneal malignant mesothelioma organs. The culture medium comprises an initial culture medium and an amplification culture medium, wherein a formula of a second culture medium comprises Advanced DMEM/F12, 1-2% of P/S double antibodies, 1-2% of primocin, 10mM of Hepes, 2-10mM of GlutaMAX, a B27 additive, an N2 additive, 50-125ng/mL of Wnt-3a, 50-125ng/mL of Noggin, 0.5-1.25 [mu] g/mL of R-Spondin1, 100-250ng/mL of FGF10, 35-70ng/mL of EGF, 1-10nM of gasin I, 5.5-10ng/mL of Insulin, 7.5-12.5 [mu The first culture medium is prepared by adding the following compounds with final concentrations on the basis of the second culture medium: 10 [mu] M of Nicotinamide, 10 to 40 [mu] M of Y-27632 and 1.75 to 3.25 [mu] M of CHIR999021. The method is high in induction rate. 本发明公开了一种腹膜恶性间皮瘤类器官的培养基和培养方法,包括初始培养基和扩增培养基:所述第二培养基的配方为:Advanced DMEM/F12,1-2%P/S双抗,1-2%primocin,10mM Hepes,2-10mM GlutaMAX,B27添加剂,N2添加剂,50-125ng/mL Wnt-3a,50-125ng/mL Noggin,0.5-1.25μg/mL
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The culture medium comprises an initial culture medium and an amplification culture medium, wherein a formula of a second culture medium comprises Advanced DMEM/F12, 1-2% of P/S double antibodies, 1-2% of primocin, 10mM of Hepes, 2-10mM of GlutaMAX, a B27 additive, an N2 additive, 50-125ng/mL of Wnt-3a, 50-125ng/mL of Noggin, 0.5-1.25 [mu] g/mL of R-Spondin1, 100-250ng/mL of FGF10, 35-70ng/mL of EGF, 1-10nM of gasin I, 5.5-10ng/mL of Insulin, 7.5-12.5 [mu The first culture medium is prepared by adding the following compounds with final concentrations on the basis of the second culture medium: 10 [mu] M of Nicotinamide, 10 to 40 [mu] M of Y-27632 and 1.75 to 3.25 [mu] M of CHIR999021. The method is high in induction rate. 本发明公开了一种腹膜恶性间皮瘤类器官的培养基和培养方法,包括初始培养基和扩增培养基:所述第二培养基的配方为:Advanced DMEM/F12,1-2%P/S双抗,1-2%primocin,10mM Hepes,2-10mM GlutaMAX,B27添加剂,N2添加剂,50-125ng/mL Wnt-3a,50-125ng/mL Noggin,0.5-1.25μg/mL</abstract><oa>free_for_read</oa></addata></record>
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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 Culture medium and culture method of peritoneal malignant mesothelioma organoid
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