shgoy-698乌药 Lindera aggregata (Sims) Kosterm.protopine异乌药内酯728-61-0C15H16O3≥98%
shgoy-699乌药 Lindera aggregata (Sims) Kosterm.Nodakenin乌药醚内酯13476-25-0C15H16O4≥98%
shgoy⁻⁷00乌头属欧乌头Aconitum napellus L.Daucosterol硬飞燕草碱509-18-2C25H41NO7≥98%
shgoy⁻⁷01乌头属欧乌头、川乌、北草乌和 华乌头AconitumGeraniin塔拉萨敏20501-56-8C24H39NO5≥98%
shgoy⁻⁷02乌头属Aconitum carmichaeli Debxcorilagin光翠雀碱26166-37-0C22H33NO3≥98%
shgoy⁻⁷03乌头属Aconitum carmichaeli Debx(E)-4-((5-Hydroxy-3,7-dimethylocta-2,6-dien-1-yl)oxy)⁻⁷H-furo[3,2-g]chromen⁻⁷-one脱氧3175-95-9C34H47NO10≥98%
shgoy⁻⁷04乌头属 Aconitum L.Cepharanthine乙酰77181-26-1C36H49 NO12≥98%
shgoy⁻⁷05乌头属 Aconitum carmichaeli Debx.7-Methoxy-1-methyl-9H-pyrido[3,4-b]indole hydrochloride中2752-64-9C33H45NO11≥98%
shgoy⁻⁷06乌头属 Aconitum carmichaeli Debxsophoridine乌头原碱509-20-6C25H41NO9≥98%
shgoy⁻⁷07乌头属 Aconitum carmichaeli Debxalpha-Boswellic acid302-27-2C34H47NO11≥98%
shgoy⁻⁷08乌头属 Aconitum carmichaeli DebxJolkinolide B甲酰新乌头原碱63238-67-5C31H43NO10≥98%
shgoy⁻⁷09乌头属 Aconitum carmichaeli Debx28-demethyl -β-amyrone硬飞燕草碱509-18-2C25H41NO7≥98%
shgoy⁻⁷10乌头属 Aconitum carmichaeli DebxOleanan-29-al,13,28-epoxy-3-[(O-b-D-glucopyranosyl-(1®2)-O-[O-b-D-xylopyranosyl-(1®2)-b-D-glucopyranosyl-(1®4)]-a-L-arabinopyranosyl)oxy]-16-hydroxy-, (3b,16a,20b)-德尔塔林6836--11-9C27H41NO8≥98%
shgoy⁻⁷11乌头属 Aconitum carmichaeli DebxIsovitexin次6900-87-4C33H45NO10≥98%
shgoy⁻⁷12乌头属 Aconitum carmichaeli DebxCyasterone印4491-19-4C34H47NO10≥98%
shgoy⁻⁷13乌头属 Aconitum carmichaeli Debx5,7-dihydroxy-4',6-dimethoxyflavone异佛手柑内酯482-48-4C12H8O4≥98%
shgoy⁻⁷14乌头Aconitum carmichaeli Debx5,7-Dihydroxy-4H-chromen-4-one甲酰次乌头原碱63238-66-4C32H45NO10≥98%
shgoy⁻⁷15乌头Aconitum carmichaelil-Chicoric acid丽江73870-35-6C35H49NO9≥98%
shgoy⁻⁷16乌头Aconitum carmichaeli(2S,3R)-2-Amino-4-hydroxy-3-methylpentanoic acid10- 羟基尼奥宁132362-42-6C24H39NO7≥95%
shgoy⁻⁷17乌头Aconitum carmichaeliECHINOCYSTIC ACID准葛尔乌头胺23179⁻⁷8-4C22H29NO3≥95%
1)贴壁细胞传代:提前将培养基、PBS放入37℃水浴锅内预热,用75%酒精擦拭后再放入超净台内,吸除或倒掉细胞瓶内旧培养液,加少量PBS润洗细胞,加入适量胰酶,使胰酶的量能盖住细胞,37℃孵育,每隔2~3min显微镜下观察,待贴壁细胞间间隙变大、细胞趋于圆形但还未漂起时弃去胰酶,加入新鲜培养基,晃动细胞瓶,终止胰酶作用,用吸管小心吹打贴壁的细胞,制成细胞悬液。控制吹打的力度,避免产生大量的气泡,将细胞悬液分别接种到另外的2~3个细胞瓶内,加入新鲜培养基,置37℃温箱培养,隔天观察贴壁生长情况。
2)悬浮细胞传代:将细胞悬液转移到无菌离心管内,1000rpm离心5min,弃去上清,加入新鲜的培养基,用吸管小心吹散沉淀,制成细胞悬液,将细胞悬液分别接种到另外的2~3个细胞瓶内,加入新鲜培养基,置37℃温箱培养。