1) NADH-6 gene
NADH-6基因
1.
Total mRNAs of domestic and wild silkworms were extracted, and COⅠ and NADH-6 genes from mtDNA were cloned by RT-PCR and analysed by DIG-RFLP method.
为了进一步明确家蚕和野桑蚕的亲缘关系,收集了中国和日本的一些家蚕和野桑蚕品种资源,提取了家蚕和野桑蚕的总mRNA,通过RT-PCR克隆了家蚕和野桑蚕线粒体DNA(mtDNA)的细胞色素氧化酶亚基1基因(cytochromeoxidasesubunit1gene,COⅠ)和NADH-6基因,并制备探针进行了DIG-RFLP检测。
2) NADH gene
NADH基因
1.
We carried out a series of studies for such inssue based on fragment length polymorphis of microsatellite locus Ple46, sequence of NADH gene on mtDNA and subspecies specific alleles at 11 microsatellites.
本论文用微卫星位点Ple46片段长度多态性、mtDNA的NADH基因序列和11个微卫星位点亚种特异性等位基因开展了一系列虎亚种鉴别方法的研究。
3) 8-(6-aminohexyl)-amino-NADH
8-(6-氨基己烷)-氨基-NADH
1.
8-(6-aminohexyl)-amino-NADH was successfully prepared by modifying NADH with 1,6-hexanediamine at the C8 position of adenine moiety.
采用1,6-己二胺对烟酰胺辅酶(NADH)的腺嘌呤C8位点进行定点修饰,通过DEAE-Sepharose层析分离得到产物8-(6-氨基己烷)-氨基-NADH。
4) ND 5 gene
NADH氧化还原酶基因(ND5)
5) ND-1
NADH脱氢酶亚单位1基因
6) bcl-6 gene
bcl-6基因
1.
Objective: To investigate the BCL-6 gene alterations in B-cell Non-Hodgkin’s lymphomas( B-NHL) in Chinese populations and its clinic-pathological significance.
目的:系统性地研究中国人B-NHL常见类型中BCL-6基因的异常,并探讨其临床病理意义。
2.
BCL-6 gene is the most relevant gene.
BCL-6基因５’端调控区极不稳定，容易变化，包括染色体间的易位、突变和缺失，可导致BCL-6表达失调。
3.
The results indicated that up-regulation of bcl-6 expression was found only in K562 cells being induced differentiating into megakaryocyte-lineage,while mutation of 5\'regulatory region of bcl-6 gene was not found.
用Western blot检测以十四烷酸佛波醇-13-乙酯(tetradecanoylphorbol13-acetate,TPA)、羟基脲(hydooxyurea,Hu)及六甲基双乙酰胺(hexamethylene bisacetamide,HMBA)为诱导剂分别诱导K562细胞向巨核细胞系、红细胞系及巨噬细胞系分化时bcl-6表达变化,用PCR、克隆、直接DNA测序方法分析bcl-6基因5′调控区序列变异情况。
补充资料：beta-NADH disodium salt
分子式：C21H27N7Na2O14P2
分子量：709.41
CAS号：606-68-8
性质：水溶性soluble。
分子量：709.41
CAS号：606-68-8
性质：水溶性soluble。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条