本发明提供了一种HBB基因的用途,用于制备判别结核潜伏感染和活动性结核的产品. The present invention provides the use of a HBB gene for the preparation of discrimination latent tuberculosis infection and active TB products. 所述判别结核潜伏感染和活动性结核的产品优选包括:用实时定量PCR或基因芯片检测判别...
Do you need HBB gene to express the HBB protein for functional or characterization studies? Get the HBB gene in an expression-ready vector for your molecular biology studies by ordering a HBB ORF clone.About the HBB gene The alpha (HBA) and beta (HBB) loci determine the structure of the ...
We have developed a cost-effective, highly sensitive and specific, indigenous targeted NGS assay for detecting mutations in the HBB gene. Using this custom NGS assay, we processed 1530 samples (3017 alleles), in which we detected a spectrum of 48 pathogenic/likely pathogenic variants (mutations)...
(5%-30%)β-globinchainsynthesis.Themostcommongeneticdefectsinβ-thalassaemiaarecausedbypointmutationsorsmalldeletionsorinsertionsinHBBgene,whichcausedasubstantialreducionofP-chainsynthesisandadistincthaematolog...
Relationships of mRNA-protein secondary structures in the human -globin gene HBB and four variants. Chin Sci Bull, 2012, 57, doi: 10.1007/s11434-012-4996-3 《中国科学》杂志社 SCIENCE CHINA PRESS 论文 人类 珠蛋白基因 HBB 及其突变体的 mRNA-蛋白质 二级结构分析 李燕飞① 云南大学现代生物学研究...
提供的HBB人源重组蛋白(Q01)产品为带有GST标签的人源HBB部分序列重组蛋白,其对应的GeneID号为3043。 产品描述 与其它公司提供的重组蛋白不同,该HBB人源重组蛋白(Q01)产品为采用CFS的无细胞麦胚蛋白合成系统表达出来的重组蛋白,可表达出对细胞有毒性、易被蛋白酶降解的蛋白;并获得具有良好的可溶性,并有翻译后修饰、...
关键词TALENs;基因治疗;腺病毒作者:**大指导老师:**顾振纶多重PCR分子诊断和p53、HBB基因点突变检测研究及艾滋病基因治疗相关前期研究英文摘要MultiplexPCRmoleculardiagnosisandmutationdetectionofp53、HBBgeneresearchandadvanceresearchofTALENsingenetherapyofAIDSPartIAbstractTheapplicationresearchofmultiplexPCRtechnologymedia...
The scientists say their method, which repairs the beta-globin gene (HBB), avoids gene therapy techniques that can introduce potentially harmful genes into cells. Researchers discover safe way to repair sickle cell disease genes In review, a point mutation in the HBB (beta hemoglobin) gene occurr...
【英文摘要】Theβ-thalassaemia is hereditary autosomal disorders with decreased(β+) or absent(β0) (5%-30%)β-globin chain synthesis.The most common genetic defects inβ-thalassaemia are caused by point mutations or small deletions or insertions in HBB gene, which caused a substantial reducion...
解释:在医学领域,HBB代表血红蛋白β链,是血红蛋白分子中的一个重要组成部分,与合成血红蛋白有关。 造句: Mutations in the HBB gene can lead to beta-thalassemia, a genetic blood disorder. (HBB基因的突变可能导致β-地中海贫血,这是一种遗传性血液疾病。) Scientists are study...