会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明授权
    • RBM3 as a marker for malignant melanoma prognosis
    • RBM3作为恶性黑素瘤预后的标志物
    • US08632984B2
    • 2014-01-21
    • US13201742
    • 2009-12-17
    • Mathias UhlenFredrik PontenKarin Jirstrom
    • Mathias UhlenFredrik PontenKarin Jirstrom
    • G01N33/53C12N5/07A61K39/395A61K38/00
    • G01N33/689C07K14/4748G01N33/5743
    • A method for determining whether a mammalian subject having a malignant melanoma belongs to a first or a second group, wherein the prognosis of subjects of the first group is better than the prognosis of subjects of the second group is provided. The method comprises the steps of: evaluating an amount of RBM3 protein in at least part of a sample earlier obtained from the subject and determining a sample value corresponding to the evaluated amount; comparing said sample value with a predetermined reference value; and if said sample value is higher than said reference value, concluding that the subject belongs to the first group; and if said sample value is lower than or equal to said reference value, concluding that the subject belongs to the second group.
    • 一种用于确定具有恶性黑素瘤的哺乳动物受试者是否属于第一组或第二组的方法,其中提供了第一组受试者的预后优于第二组受试者的预后。 该方法包括以下步骤:评估早期从受试者获得的样品的至少部分中的RBM3蛋白的量,并确定与评估量对应的样品值; 将所述样本值与预定参考值进行比较; 并且如果所述样本值高于所述参考值,则认定所述对象属于所述第一组; 并且如果所述样本值低于或等于所述参考值,则认定所述对象属于所述第二组。
    • 8. 发明授权
    • Method of sequencing DNA
    • DNA测序方法
    • US06210891B1
    • 2001-04-03
    • US09269436
    • 1999-07-06
    • Pål NyrenMathias UhlenMostafa Ronaghi
    • Pål NyrenMathias UhlenMostafa Ronaghi
    • C12Q168
    • C12Q1/6869C12Q2565/518C12Q2565/301C12Q2535/101
    • The present invention provides a method of identifying a base at a target position in a single-stranded sample DNA sequence wherein an extension primer, which hybridizes to the sample DNA immediately adjacent to the target position, is provided and the sample DNA and extension primer are subjected to a polymerization reaction in the presence of a deoxynucleotide or dideoxynucleotide, whereby the deoxynucleotide or dideoxynucleotide will only become incorporated and release pyrophosphate if it is complementary to the base in the target position. Release of pyrophosphate is detected enzymatically and pyrophosphate detection enzyme(s) are included in the polymerization step.
    • 本发明提供了在单链样品DNA序列中鉴定目标位置的碱基的方法,其中提供了与紧邻目标位置的样品DNA杂交的延伸引物,并且样品DNA和延伸引物为 在脱氧核苷酸或双脱氧核苷酸的存在下进行聚合反应,由此脱氧核苷酸或双脱氧核苷酸仅在靶位置与碱基互补时才被引入并释放焦磷酸盐。 检测到焦磷酸盐的释放,聚合步骤中包括焦磷酸盐检测酶。