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虎纹涡虫姐妹染色单体的差异染色

Differential staining of Dugesia tigrina sister chromatids.

作者信息

Edelman J R, Lin Y J

机构信息

Department of Biology, Long Island University, Brooklyn Center, New York 11201.

出版信息

Cytobios. 1994;78(313):123-8.

PMID:7520850
Abstract

Planaria were cultured in a solution of bromodeoxyuridine (BrdU) for 24 h in an attempt to produce sister chromatid differential staining (SCD) and sister chromatid exchange (SCE). SCD was produced when planaria were cultured in planarian saline solution (PSS) containing 5 x 10(-5) M BrdU. Colchicine (0.02%) was added to the BrdU/PSS culture medium 8 to 10 h before sacrifice. Animals were then vigorously dissociated into cells, centrifuged, and fixed in Carnoy's solution. Slides were prepared using the air-drying method, allowed to age for at least 1 day, stained with the fluorochrome Hoechst 33258, exposed to high intensity incandescent light, stained with Giemsa solution, and mounted. This method is the first reported SCD/SCE investigation in the Platyhelminthes and consistently yielded second division metaphases exhibiting SCD and third division metaphases exhibiting non-reciprocal SCE's composed of unifilarly BrdU-labelled DNA.

摘要

将涡虫培养在溴脱氧尿苷(BrdU)溶液中24小时,试图产生姐妹染色单体差异染色(SCD)和姐妹染色单体交换(SCE)。当涡虫在含有5×10⁻⁵ M BrdU的涡虫生理盐水溶液(PSS)中培养时,可产生SCD。在处死前8至10小时,向BrdU/PSS培养基中加入秋水仙碱(0.02%)。然后将动物剧烈解离成细胞,离心,并固定在卡诺氏固定液中。使用空气干燥法制备载玻片,使其老化至少1天,用荧光染料Hoechst 33258染色,暴露于高强度白炽灯下,用吉姆萨溶液染色,然后封片。该方法是首次报道的针对扁形动物的SCD/SCE研究,并且始终产生显示SCD的第二次分裂中期以及由单链BrdU标记DNA组成的显示非相互性SCE的第三次分裂中期。

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