shgoy-473雪松Cedrus deodaraCrocin9ALPHA,13ALPHA-表二氧基松香-8(14)-烯-18-酸116499-73-1C20H30O4≥95%
shgoy-474雪松Cedrus deodara2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one4-羟基苯丙酮, 对羟基苯丙酮70-70-2C9H10O2≥95%
shgoy-475雪松Cedrus deodara1-Deoxynojirimycin异海松酸5835-26-7C20H30O2≥96%
shgoy-476雪胆 Hemsleya amabilis Dielsb-D-Xylopyranoside,3-(6,7-dihydro-6-hydroxy-7,7-dimethyl-5H-furo[3,2-g][1]benzopyran-2-yl)-5-hydroxyphenyl豆腐果新苷A496066-82-1C32H38O19≥98%
shgoy-477玄参科植物地黄 Rehmannia glutinosamulberroside A地黄甙 A81720-05-0C21H32O15≥98%
shgoy-478玄参 Scrophularia ningpoensis Hemsl.Sanggenon C安格洛苷C115909-22-3C36H48O19≥98%
shgoy-479玄参 Scrophularia ningpoensis Hemsl.Sanggenon D苦玄参苷IA97230-47-2C41H62O13≥98%
shgoy-480续随子Euphorbia lathyris L.scopolin环氧续随子醇28649-60-7C20H30O5≥98%
shgoy-481续随子Euphorbia lathyrismorusin绿玉树因子TI276376-43-7C32H40O8≥95%
shgoy-482续随子Euphorbia lathyrisasiatic acid2,5,7,8,9,14-六乙酰氧基-3-苯甲酰基氧基-15-羟基-6(17),11E-麻风树属二烯210108-86-4C39H50O15≥95%
shgoy-483续随子Euphorbia lathyrisTectoridin2,5,14-三乙酰氧基-3-苯甲酰基氧基-8,15-二羟基-7-异丁酰氧基-9-烟酰氧基氧基-6(17),11E-麻风树属二烯210108-87-5C43H53NO14≥95%
shgoy-484续随子Euphorbia lathyrisTectorigenin2,5,9,14-四乙酰氧基-3-苯甲酰基氧基-8,15-二羟基-7-异丁酰氧基-6(17),11E-麻风树属二烯210108-88-6C39H52O14≥95%
shgoy-485续随子Euphorbia lathyrisdihydrocapsaicin2,5,7,14-四乙酰氧基-3-苯甲酰基氧基-8,15-二羟基-9-烟酰氧基-6(17),11E-麻风树属二烯210108-89-7C41H49NO14≥95%
shgoy-486续随子Euphorbia lathyrisTetrandrine210108-91-1C37H48O13≥95%
shgoy-487续随子Euphorbia lathyrisFangchinoline670257-89-3C43H51NO15≥95%
shgoy-488续断 Himalayan Teasel RootSinomenine hydrochloride木通皂甙 D; 川续断皂苷VI39524-08-8C47H76O18≥98%
shgoy-489续断 Himalayan Teasel Rootcapsaicin川续断皂苷乙33289-85-9C53H86O22≥98%
shgoy-490绣球Hydrangea macrophylla[4,8'-Bi-2H-1-benzopyran]-3,3',5,5',7,7'-hexol,2,2'-bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-, (2R,2'R,3R,3'R,4R)-(2S,2'S,3R,3'R,4R,4'S)-4,4'-((1E)-1-甲酰基-1_-丙烯基-1,3-二基)双(3-乙烯基-2-471271-55-3C34H46O19≥95%
shgoy-491绣球Hydrangea macrophyllaTetrahydropalmatine hydrochloride罗布麻酚 A358721-33-2C13H20O3≥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。