gene test 中文意思是什麼
gene test
解釋
基因檢測-
Because traditional epistasis measure methods can only reflect the extent of interaction between all genes in the chromosome, we used correlation length analysis and epistasis measures on the fitness landscapes of schemata to test the extent of interdependence between some certain gene loci in study
針對傳統的測試基因關聯的方法只能給出染色體中所有基因位的整體關聯程度的情況，通過在模式適應值曲面上分別進行相關長度測試和基因關聯測試，以研究染色體中一些特定位之間的基因關聯程度。 -
To test the p7 promoter activity, a series of constructs were obtained by cloning the different dna fragments into the luciferase gene reporter vector pgl3 - b. when the constructs were transiently transfected into thp - 1 cells, luciferase activity assay showed that the core region of p7 promoter located at - - 165 bp
第一部分的工作首先通過對人acat - 1基因p7啟動子序列進行5 '和3 ' -端的缺失的詳細分析，結果顯示最大報告基因轉錄表達活性位於- 612 - 165bp區段。 -
By using the complementation test an unknown mutant can be rapidly assigned to a particular gene.
採用互補測驗可迅速地將某一未知突變型歸屬于某一特定基因。 -
In this paper, 45 e. coli strains isolated from chicken farms in sichuan province were determined to be the pathogenic e. coli by animal test. type 1 pili of 45 strains isolated was detected by msha. the pila gene of 45 avian pathogenic e. coli strains were amplified by the polymerase chain reaction ( pcr ) with primers designed according to the sequence of the pila gene in genbank. results showed that pcr was more sensitive, faster and more characteristic than msha to detect type 1 pili
本研究將從四川規模化雞場分離鑒定、經1日齡雛雞致病性試驗得到的雞源致病性大腸桿菌45株，採用d -甘露糖敏感血凝試驗（ msha ）檢測1型菌毛，根據genbank中公布的人源大腸桿菌1型菌毛pila基因序列設計一對引物用pcr擴增雞源致病性大腸桿菌1型菌毛pila基因。 -
Heredity modes of 6 traits were studied by analysis of population genetics, by the method of family combination analysis, by the methods of proband ' s sib analysis, segregation analysis, the threshold model of polygenes, and analysis of typical family trees, according to the data of the 72 families. the relative importance between genetic and environmental effect on each character was evaluated by comparing the coherence of twins. gene frequencies of 5 genetic characters, calculated from han group in huhhot, were compared with other groups by u - test so as to study the population or nationality difference in heredity
採用群體遺傳學分析、家系組合分析法、先證者同胞法、分離分析法及多基因閾值模式分析方法對所得家系資料進行了統計學分析，結合家繫系譜分析探討了上述6項特徵的遺傳方式；通過雙生子一致率的比較，對上述特徵的遺傳與環境效應的相對重要性進行了評價；計算了呼和浩特市漢族群體5對遺傳性狀的基因頻率，採用u檢驗方法與相關文獻報道的其他群體進行了比較，探討了不同種族間或民族間的遺傳差異性。 -
Pcr and enzyme acitivity check on chitin agar showed that the chitinase gene fragment existed and expressed in the wildtype strains. antagonistic activity test in vitro suggest that the transformants remained the ability to produce antibiotics. the recombinant strains showed an increased biocontrol efficacy against wheat take - all and rhizoctonia sheath blight in greenhouse
對小麥全蝕病和紋枯病的盆栽試驗結果表明工程菌株p25113一9的防病作用強於野生菌株，尤其是對小麥全蝕病的防治作用，其防治效果同野生菌株ap113和ap25相比，分別增長了22 -
It still remains a question whether the rearrangements of igh come from h / rs cell or the background lymphocytes. in this study, we have detected the igh clonal correlation between the h / rs cells and the background cells, from a new aspect to study the clonality of h / rs cell and its relation with the background cells. the expression of b - cell - specific activator protein ( bsap ) was detected in hl. igh gene rearrangements were analysed by the methods including gene analysis in neoplasms tissue and micropicked cells from paraffin - embedded sections, sequencing to test the pcr product, and in situ pcr
本研究將在以往研究的基礎上，在國內率先把b細胞核反式作用因子? b細胞特異性激活蛋白（ b - cell - specificactivatorprotein ， bsap ）應用於hl的研究，檢測hl的bsap表達，並採用石蠟刮片組織和微切割單細胞的基因分析、測序分析和間接原位pcr等方法，同步觀察分析h rs和背景淋巴細胞的igh基因克隆相關性，從又一個新視角探究chl的腫瘤性h rs細胞克隆性及與背景淋巴細胞的關系。 -
( 4 ) transformation of mdmv - cp gene mdmv - cp gene was successfully into r18. w18 and 501 in 2001 fall, each material being bombed 20, 15, and 10 plates. 213 bastar ( effective constitution ppt ) resistant plants were obtained of which r18, w18 and 501 resistant plants counted 103, 90, and 20 plants respectively. molecular test was undergoing
O ） mdmvcp因的邀傳轉化於2001年秋用基因槍將mdmvcp基因巾35scpbar質粒）導入、 w18 、 501三個優良自交系，利用已建立好的遺傳轉化體系，經抗性篩選、分化、壯苗等步驟，已得到抗bastar （有效成分ppt ）植株213棵，其中r18103株、 w1890株、 50120株。 -
97 % identities in amino acids respectively. the e. coli strain dh5 transformed recombinant plasmid phn was induced with 0. 6 mmol / m iptg for n gene expression. the expressed product was identified by sds - page and westem - blot test, a fusion protein about 47ku as we expected was found
將含有重組質粒phn的菌株dh5在37條件下培養，以濃度為0 . 6mmol / liptg誘導，重組質粒n基因phn融合蛋白獲得了表達：經sds - page ， western - blot試驗，確定其表達的融合蛋白產物大小為預期的47ku 。 -
Last october, scientists field - tested a cotton pest called the pink bollworm moth, carrying a test gene for a glowing jellyfish protein
去年10月科學家對一種叫紅棉鈴蟲蛾的棉花害蟲做了野外試驗，它帶有一個發光的水母蛋白測試基因。 -
The insect feeding test indicated that the development of lymantria dispar was clearly put off, in which the insects feeded transgenic plants were 2 ages, when the insects as the control were 4 ages after treating 15 days. besides, the insect growth was restrained, that the weight of insect as control was 9. 7 and 6. 4 times compared to the treated ones. it also resulted that the foreign gene could normally express in the transgenic plants by displaying insect resistance in a certain degrees
舞毒蛾幼蟲發育推遲， 15天時處理為4齡，但對照仍為2齡，發育推遲了2個齡期；舞毒蛾生長受到抑制，對照的體重為處理的9 . 7倍與6 . 4倍，外源基因嚴重抑制幼蟲的生長，說明外源基因在轉基因白樺中能夠正常表達，轉基因植株表現一定的抗蟲性。 -
Through studying the working mechanism of the composing, the paper referred the bearing ' s analyzing model and designing flow. through shearing test of high damping rubber, the paper analyzes the influence of shearing shape, shearing strain range and inspiriting frequence on the characteristic parameters ( dynamic shear elastic module, dissipation engineering module, wasted gene ). according to the rule of equivalent energy, the paper gets the hysteretic curve of hdr ' s equivalent bilinear model and parameters ' calculating formula
本論文通過對這種分離式減震支座各組成部分工作機理的研究，提出了該分離式減震支座整體的計算分析方法和設計流程；通過高阻尼橡膠剪切試驗，分析了高阻尼橡膠剪切面形狀、剪應變幅值、激勵頻率和試件高度對特徵參數（動態剪切彈性模量、耗能模量、損耗因子）的影響。 -
" gene patents give their owners property rights over gene sequences for example in a diagnostic test, as a test for the efficacy of a new drug, or in the production of therapeutic proteins, " murray said
其中，享有人類基因專利權最多的是美國incyte制藥公司，其享有的專利權覆蓋了2000種人類基因。對此，莫里教授表示，基因專利權給它的所有者帶來了基於這種基因某些新用途的財產權。 -
Test data sets and evaluation of gene prediction programs on the rice genome
水稻基因組中預測基因的程序評估及測試數據集 -
The protein product of meq gene was highly expressed in the nuclei of recombinant baculovirus infected sf9 cells when using an anti - meq monoclonal antibody ( mcab ) 23b46 to run the immunofluorescence assay ( fa ) ; the expression quantity and if staining patterns differed with different times post - infection ( pi ). the results of western blotting and immunoprecipitation test showed there were two specific bands around 60 kd. the results of the study demonstrated that the baculovirus / insect cell system is effective to be used to express nuclear protein of virus
結果發現:本表達系統產生的meq蛋白可被重組痘病毒表達的meq制備的單抗23b46所識別;在感染細胞中， meq蛋白僅局限於細胞核內，而且隨著感染后（ pi ）時間的增加，具有從核質向核仁和核膜轉移的趨向; w已stemblot和免疫沉澱試驗均證實重組桿狀病毒感染細胞裂解物中出現有兩條大小約為60kd的特異帶。 -
Cea gene was transferred into human dcs, and specific anti - cancer effecs induced by the vaccine was observed. this test is part of my tutor ' s. hang you - tian has observed the induction of crcinembryonic antigen ( cea ) - specific cytotoxic t - lymphocyte responses in vitro when he transfected dcs with pcdna3 - cea, and has observed the immunity effects of the dcs ( pcea ) inoculateing against to ct 26 ( hcea + ) loaded in balb / c mice. after vaccination with the cea gene - modified dc, the survival time of the mice vaccinated with ct26 + ( cea + ) ws prolonged more potently than that of the mice vaccinatd with other dcs
癌胚抗原（ carcinoebryonicantigen ， cea ）是一種研廠鄭州大學2002年碩士畢業論文轉染人癌胚抗原真核表達質粒的人樹突狀細胞的抗瘤作用究最為深入的腫瘤相關抗原（ tumorassociatiednigen ， taa ） ，在90的胃腸道腫瘤、 50的乳腺癌及70的非小細胞肺癌中有高水平的表達，是目前國際上公認的腫瘤標志物。 -
Probing into the method of prompt test of herbicide sethoxydim - resistant gene flow
快速檢測抗除草劑拿捕凈基因流的方法初探 -
No trace of any newly expressed protein band was noticed in supernant as well as in the cells by sds - page, except the verification of the substitution of beta - galactosidase gene ( the lose of galactosidase protein band ), which is a selective marker of the wild - type virus. elisa test results suggested the expression of egf in cells, but not in culture supernant. the quantitative calculation suggested the expressed egf was about 6 - 7 u g ( as egf standard ) per flask ( 2 > < 106 cells ) in the cellular extract
將重組病毒rbmbacph - egf以10moi感染bmn細胞， 72小時后收集培養細胞和上清；培養上清和經超聲波處理的細胞樣品elisa檢測發現胞內樣品中存在能與egf抗體免疫反應的產物，粗略估計表達量約6 7 g 2 10 ~ 6個細胞（相當于egf標準品） ；重組病毒rbmbacph - egf穿刺接種5齡家蠶幼蟲，每隔24h收集蠶血淋巴，經elisa檢測發現第4天表達量最高，根據egf標準曲線計算蠶血淋巴的表達量約32 g ml ； elisa定性實驗還發現正常蠶血也存在與egf抗體間交叉反應的物質。 -
Standard guide for measuring the presence of planar organic compounds which induce cyp1a, using reporter gene test systems
用指示器基因測試系統測定感應cyp1a的共面有機化合物的存在的標準指南 -
Harmon, amy. " as gene test menu grows, who gets to choose ? " new york times 21 july 2004
隨著基因測試項目的發展，誰來選擇？ ， 《紐約時報》 ， 2004年7月21日
分享友人