點染色 的英文怎麼說
中文拼音 [diǎnrǎnshǎi]
點染色
英文
vertex coloring-
At anaphase the dicentric chromatid will form a bridge and the acentric a fragment, both of which can be scored.
在後期雙著綠點染色體將形成一個橋,無著綠點染色體單體形成一斷片,此兩者均可記錄下來。During mitosis, sister chromatids remain joined by their centromere until anaphase
在有絲分裂期間,姐妹染色單體在分裂後期之前都是通過著絲點連接的。In meiosis it is not until anaphase ii that the centromere divides, the chromatids being termed daughter chromosomes after separation
在減數分裂期間,直到分裂後期ii兩條染色單體才隨著著絲點的分裂而彼此分開。Each chromosome consists of two chromatids held together by the centromere.
每個染色體由兩個染色單體所組成,它們被一個著絲點聯結在一起。During anaphase ii the centromeres divide and single chromatids are drawn toward the poles, thus sister chromatids are separated
在減數分裂後期ii ,每條染色體的兩個染色單體隨著著絲點的分裂而彼此分開,由紡錘絲牽向兩極。A locus is the "location" of a gene along a chromosome.
位點是基因在染色體的位置。Chromosome 5 is distinguished by a proximal knob.
第5染色體的特點是有一個近側的節結。Textiles - tests for colour fastness - part z11 : evaluation of speckiness of colorant dispersions
紡織品.色牢度試驗.第z11部分:染色劑擴散斑點的評價Textiles - tests for colour fastness - part z11 : evaluation of speckiness of colorant dispersions iso 105 - z11 : 1998 ; german version en iso 105 - z11 : 2000
紡織品.色牢度試驗.第z11部分:染色劑分散斑點評定Y chromosome is transmitted in the form of hap - loid, leading to extreme disequilibrium of y chromosome genetic markers distribution in different population. the prerequisite of str application in forensic medicine is establishment of a database of population y - str loci haplotype distribution. therefore we need to form haplotypes by using the known highly polymorphic str loci and detect more local population
由於y染色體呈單倍體遺傳,導致y染色體遺傳標記在不同人群中的分佈極不平衡,群體差異比常染色體str位點更加顯著,在法醫學應用的前提條件是:建立含有多個y - str位點的單倍型的群體分佈數據庫。That is, if we want to assign frequencies to a pair of adjacent cities or radio stations, then the difference of those two frequencies used has to avoid the set t. the t - colorings of multigraphs is a more practical case of t - colorings of graphs where interference may occur on different level
頻率分配問題的圖論模型可以這樣得到:令收發信機為圖中的點,兩點之間有邊當且僅當這兩個收發信機干擾。重圖的t -染色是圖的t -染色的一個較為實用的部分,這是因為在研究頻率分配時,干擾可能會在不同的水平上發生。8p22 of human chromosome is an region with abundant disease - related genes. it is said that it is susceptible loci of hypertension and schizophrenia. the region is also the loci of oncogene and tumor su - pressor gene
人染色體8p22區是疾病基因富含區域,有報道說該區域是高血壓、精神分裂癥等疾病的易感位點,也是癌基因和抑癌基因的研究熱點。The nuclei are ooid or round with finely reticular chromatin and rare punctate nucleoli. the cytoplasm is pale eosinophilic or clear
細胞核呈圓形或卵圓形,染色質為精細的網路狀,稀疏的斑點狀核仁。胞漿蒼白色或透明,嗜酸性染色。4. engineering dhqase ( arod ) - deficient e. coli mutant with a second copy of the arob gene gene targeting technique was used to disrupt the arod gene in e. coli chromosome. the mutant 31bk was engineered, in which homologous recombination of the arobkanr gene cassette into the arod locus ( arod : : arobkanr ) of the e. coli strain atcc31884 genome utilized the helper plasmid pkd46 with red system. the host cell 31bk lacked catalytic activity of dhqase ( arod ) and had a second copy of the arob gene, so it improved carbon flow into the quinic acid biosynthesis direction
構建宿主菌基因精確定位突變株31bk ( arod : : arobkan ~ r )為了改變代謝途徑脫氫奎尼酸( dhq )分支點上的代謝流量,使之充分流向目的產物奎尼酸合成方向,利用基因打靶技術構建了31884宿主菌arod基因精確定位插入突變體,使dhq脫水酶( dhqase )失活,阻斷了碳代謝流流向芳香氨基酸生成的方向,同時用同源重組的方法將arob基因定位整合入染色體上,解除了限速酶對碳代謝流通過共同途徑到達dhq的阻遏影響,並減輕代謝負擔。I love red maples, swaying in the sough autumn wind. it absorbs heat and gives the cold world warm color with its own life
我愛紅楓,它飄搖于肅殺的秋氣之中。它吸盡了熱,用自己的生命,給寒冷的世界點染了一片暖色。“ well, i have now, ” he said, shocked and offended. lisa would never have said such a thing, any more than she would have worn splashy tie - dyed orange
「好啦,現在我已經聽說過啦, 」他吃驚地受了冒犯地說。莉莎從來都不會說出這等話來,正如同她從來都不會穿那種有點顏色四濺扎染的橙色連衣裙。There are 4 pairs central - region - kinomere chromosomes and 4 pairs subcentral - region - kinomere chromosomes and only one pair telochromosomes in one cell
4對為中部著絲點染色體, 4對為近中部著絲點染色體,只有1對近端部著絲點染色體。Transposable elements, or insertion elements, are dna sequences which can be inserted into many different sites in chromosomes.
轉位因子或插入因子是能夠插入到染色體不同位點的DNA序列。Transposable elements, or insertion elements, are dna sequences which can be inserted into many different sites in chromosomes
轉位因子或插入因子是能夠插入到染色體不同位點的dna序列。A color a e x is legal for an uncolored vertex v e v if by coloring v with a, the subgraph induced by all vertices of color a has maximum degree at most d
對頂點v是合法的,是指由所有染顏色。的頂點導出的子圖的最大度至多是d ,其中alice和bob每走一步都是用合法顏色染未染色點。分享友人