染色的例句大全

Rapid detectin of chromosome rearrangement in medical diagnostic X-ray workers by using fluorescence in situ gybridization and Study on dose estimation.

用荧光原位杂交快速检测医用诊断x射线工作者染色体结构重排及其剂量估算的探讨。

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A nucleus can have only one y-chromosome.

一个核可以仅有一个y染色体。

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This is a Cryptococcus neoformans meningitis stained with GMS to reveal the nuclei.

新型隐球菌脑膜炎GMS染色法显示细胞核.

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Histochemical staining showed the temporary expression rate of GUS gene reached more than 70 %.

组织化学染色结果表明:GUS基因的瞬时表达率可以达到70%以上.

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Histochemical staining showed the temporary expression rate of GUS gene reached more than 70 %.

组织化学染色结果表明:GUS基因的瞬时表达率可以达到70%以上.

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Hepatolenticular degeneration ( HLD ) is an autosomal reoessively inherited disease caused by copper metabolic dysfunction.

肝豆状核变性 ( Hepatolenticulardegeneration,HLD ) 是一种铜代谢紊乱而引起的常染色体隐性遗传的疾病.

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Methods Scale placed on slide with the 10 % KOH, Parker ink was added and observed under microscope.

方法　将病损皮屑置于10%KOH玻片上后, 再加派克墨水染色,显微镜下观察.

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Methods Scale placed on slide KOH, Parker ink was added and observed under microscope.

方法将病损皮屑置于KOH玻片上后, 再加派克墨水染色,显微镜下观察.

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After having been treated with VitE and L-NBP, caspase-3-IR neurons in all four groups decreased significantly ( P < 0.01 ).

缺氧组caspase蛳3阳性染色显著增加 ( P<0.01 ).

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The paper focused on the effect of LTP treatment on dyeing and shrink proof behaviour.

重点论述了LTP技术对羊毛纤维的染色性能和防毡缩性能的影响.

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Objective To establish a quick and easy method for SDS-PAGE protein staining.

目的建立一种快速,简易的SDS-PAGE染色方法.

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METHODS: MTT assay and immunohistochemical staining method were used to detect the activity of the proliferation and metabolic status of human bladder cancer BIU 87 cells and the expression of proliferating cell nuclear antigen ( PCNA) after the BPD MA were activated by laser.

方法采用亚甲基噻唑蓝（MTT）法和免疫组化染色法检测激光活化BPD-MA后人膀胱癌细胞株BIU-87细胞增殖代谢活性及增殖细胞核抗原（proliferating cell nuclear antigen，PCNA）的表达。

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The expression of Nogo protein-A in the brain of MCAO rats was observed by in situ hybridization and the section was subjected to image analysis to determine the mean staining gray.

原位杂交法观察大脑中动脉闭塞大鼠脑内勿动蛋白-A的表达，并对切片进行图像分析，测定染色平均灰度。

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Infarcted sizes in heart were determined by dual staining with Evans-blue and TTC.

以Evans蓝和TTC双重染色方法测量心肌梗死面积.

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Osteogenesis imperfecta ( OMIM 166200) is an autosomal dominant disorder characterized by bone fragility and abnormalities of connective tissue.

成骨不全病（OMIM166200）是一种常染色体显性遗传病，其临床表现以骨折及结缔组织异常为特征。

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Background Familial benign chronic pemphigus or Hailey-Hailey disease ( HHD; OMIM 169600) is a rare autosomal dominant cutaneous disorder characterized by recurrent vesicles and erosions mainly in intertriginous areas.

研究背景：家族性慢性良性天疱疮，又称Hailey-Hailey病（HHD，OMIM169600）是一种罕见的常染色体显性遗传性皮肤病。

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Van der Woude syndrome ( VWS, OMIM 119300) is an autosomal dominant craniofacial disorder characterized by pits of the lower lip, hypodontia and cleft lip and/ or cleft palate.

范德伍兹综合征（Van der Woude syndrome，VWS，OMIM119300）是一种常染色体显性遗传病。其特征是家族性下唇瘘复合唇裂或腭裂，1／4的患者伴有缺牙（Hypodontia）。

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Method It was used by immunohistochemical PAP method.

方法使用常规HE染色及免疫组化PAP法。

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In addition, certain problems of PAP staining were discussed.

另外讨论了有关PAP法染色的几个问题。

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Objective: Effects of the preservative Potassium sorbate on micronuclei and chromosomal aberrations in root tip cells of Vicia faba and inhibition of β-carotene 、 vitamin B2 and vitamin C on genetic toxicity induced by Potassium sorbate were studied.

目的研究防腐剂山梨酸钾对蚕豆根尖细胞微核和染色体畸变的影响及β胡萝卜素、维生素B2和维生素C对山梨酸钾遗传毒性的抑制作用。

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