1) Nanjiang Yellow-goat
南江黄(山)羊
2) Boer×Nanjiang Yellow F1 hybrids
波尔山羊×南江黄羊F1代
3) Nanjiang yellow goat
南江黄羊
1.
Comparative study of genetic polymorphism from Nanjiang yellow goats by AFLP and RAPD;
南江黄羊基因组DNA的AFLP和RAPD研究
2.
Systematic breeding of Nanjiang Yellow goat;
引进的南江黄羊系统选育研究
3.
Grazing behavior of 4-month old Nanjiang yellow goat ram;
南江黄羊4月龄公羊放牧行为观测
4) Nanjiang Huang goats
南江黄羊
1.
The genotypes of 405 Nanjiang Huang goats at exon 3 of GH gene were detected by PCR-SSCP.
本试验采用PCR-SSCP方法检测405只南江黄羊GH基因外显子3多态性,并与生长性状进行关联分析。
2.
The genotypes of 392 Nanjiang Huang goats and 49 Boer goats at 5 flanking region of GHR gene were detected by PCR-SSCP.
试验采用PCR-SSCP方法检测392只南江黄羊和49只波尔山羊GHR基因5′-调控区多态性,并与体重性状进行关联分析。
5) Nanjiang huang goat
南江黄羊
1.
According to the LHβ gene sequence of cow,sheep and pig in GenBank,the primers were designed and partial sequence of LHβ gene from 35 Nanjiang Huang goat blood samples were amplified and sequenced by PCR method(GenBank No:AY853264).
参照GenBank中发表的奶牛、绵羊和猪LHβ基因序列设计引物,以35只南江黄羊为研究对象,利用PCR技术扩增并测定了山羊LHβ基因部分序列(GenBank登录号:AY853264),并利用GenBank中不同物种LHβ基因的部分编码区序列进行了系统发育分析。
2.
Using 246 Nanjiang huang goats as materials and according to the LHβ gene sequence of bovine,sheep and pig,the primers were designed,the polymorphism of LHβ gene from Nanjiang huang goat was studied by PCR-RFLP(restriction enzyme SphⅠ).
根据GenBank中公布的牛、绵羊、猪等动物LHβ基因序列设计引物,采用PCR扩增并以SphⅠ酶切分析了南江黄羊(246只)LHβ基因部分序列,比较了不同基因型的繁殖性能。
3.
According to the FSH β gene sequence of bovine and sheep,the primers were designed and follicular-stimulating hormone(FSH) β gene in-1 from Nanjiang Huang goat was sequenced.
利用牛、绵羊等动物FSHβ亚基基因序列设计引物,采用PCR法扩增并测定出南江黄羊FSHβ亚基基因内含子1全序列(GenBank登录号:AY838283)。
6) Nanjiang-Huang goat
南江黄羊
1.
Sequencing and analyzing of follicular-stimulating hormone beta subunit gene in-1 from Nanjiang-Huang goat;
南江黄羊FSHβ亚基基因内含子1序列的测定及分析
2.
According to the LHβ gene sequence of bovine,sheep and pig,the primers were designed,and the polymorphism of LHβ gene from 246 Nanjiang-Huang goat was studied by PCR-RFLP(restriction enzyme SphI).
以南江黄羊246个个体作为研究材料,利用GenBank中公布的牛、绵羊、猪等动物LHβ亚基基因序列设计引物,扩增并采用Sph I酶切分析山羊LHβ基因,比较不同基因型的繁殖性能。
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