sterile spikelet 中文意思是什麼
sterile spikelet
解釋
不結實的小穗-
Combination of additive effects and interaction effects can account for over 50 % of genotypic variation in spikelet number per spike ( sns ) and spike number per 50cm row ( snr ), and over 40 % in fertile spikelet number per spike ( fsns ), 1000 grain weight ( kgw ) and ear length ( el ), over 30 % in plant height ( ph ), over 20 % in sterile spikelet number per spike ( ssns ) and less than 10 % in grain weight per 50cm row ( gwr ) and grain number per spike ( gns )
加性效應和互作效應聯合起來，可以解釋群體總小穗數和50cm行長穗數變異的50以上，結實小穗數、千粒重和穗長變異的40以上，株高的30以上，不孕小穗數的20以上，而只能解釋50cm行長粒重和穗粒數變異的10以下。 -
57 protein spots out of about 1000 detectable spots on the 2 - d gels were indentified by the following two methods : l ) n ~ terminal edman degradation microsequencing after the protein spots were electro - transferred to pvdf membrane. 2 ) maldi - tof - ms peptide fingerprint analysis of the protein spots and protein database searching. the 2d protein maps of the rice spikelet during the sterile and fertile stages were compared
二是通過原位酶解，抽提蛋白質片段進行maldi - tof質譜分析，利用肽質量指紋圖數據在數據庫中進行檢索，在雙向電泳凝膠上取了57個點進行分析，有34個蛋白質點在數據庫得到歸屬鑒定。 -
( 4 ) the results of qtl mapping indicated that the inheritance of yield traits was very complex, the explanation as follows : additive effects except for sterile spikelet number per spike ( ssns ), qtls of additive effects were tested for all other traits, with 10 qtls for 1000 grain weight ( kgw ). the large variance of the effect values and the contribution rate of qtls indicated that the effects are difference for different qtls
14 。 （ 4 ）通過對產量性狀qtls作圖，發現產量性狀的遺傳非常復雜，可以從4個方面說明：加性效應除不孕小穗數外，各性狀均檢測到了表現加性效應的qtls 。其中，在各環境聯合分析下，檢測到了10個千粒重qtls ，各qtls的加性效應值和對群體變異的貢獻率也存在很大差異，說明不同的qtls不是等效的。 -
Indentificatiort is also the first step towards studies on protein co - and post - translational modification, and ultimately, function. in the present study, the total proteins of the photo - thermo sensitive genie male - sterile rice ( oryza sativa, peiai64s ) spikelet at meiosis stage were used as the material. by optimizing crucial factors and procedures such as sample treatment, electrophoresis parameters, and gel concentration, 2 - d maps with high quality and reproducibility were obtained
用兩種方法對經雙向電泳分離的凝膠上的蛋白質點進行了初步鑒定，一是通過電印跡轉移把蛋白質轉到pvdf膜上，再用edman降解的方法測得部分相對分子質量在10000 - 30000da的蛋白質點的n -端序列，通過網上搜索其同源性對其進行鑒定，並確定該點在凝膠上的位置。
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