摘要:
Human cell surface molecules CD70 and CD203c are expressed at higher levels in kidney carcinomas, particularly renal cell carcinomas and clear cell renal cell carcinomas, yet are expressed at low levels in normal kidney and other diseased kidney tissue, and at low levels in other tissues. CD70 and CD203c show specificity towards kidney carcinomas, particularly renal cell carcinomas and clear cell renal cell carcinomas and thus can be used as diagnostic markers and therapeutic targets for these diseases. In addition, antibodies or small molecules against these molecules could be used in treatments towards these diseases.
摘要:
Nucleic acid arrays and methods of using the same for concurrent or discriminable detection of different strains of a non-viral species. In many embodiments, the nucleic acid arrays of the present invention include probes that are specific to different respective strains of a non-viral species. In many other embodiments, the nucleic acid arrays of the present invention include probes that are common to two or more different strains of the non-viral species. In one embodiment, the non-viral species is Staphylococcus aureus, and the different Staphylococcus aureus strains include COL, N315, Mu50, EMRSA-16, MSSA-476, and 8325 strains. In another embodiment, a nucleic acid array of the present invention includes polynucleotide probes capable of hybridizing under stringent or nucleic acid array hybridization conditions to respective sequences selected from SEQ ID NOs: 1 to 7,852, or the complements thereof.
摘要翻译:核酸阵列及其用于同时或可区分检测非病毒物种的不同菌株的方法。 在许多实施方案中,本发明的核酸阵列包括对非病毒物种的不同相应菌株特异的探针。 在许多其它实施方案中,本发明的核酸阵列包括两种或多种非病毒物种的不同菌株共有的探针。 在一个实施方案中,非病毒物种是金黄色葡萄球菌,不同的金黄色葡萄球菌菌株包括COL,N315,Mu50,EMRSA-16,MSSA-476和8325菌株。 在另一个实施方案中,本发明的核酸阵列包括能够在严格或核酸阵列杂交条件下与选自SEQ ID NO:1至7,852的各序列或其互补序列杂交的多核苷酸探针。
摘要:
The present invention includes methods of normalizing hybridization reactions that are designed to select normalization control genes, specifically 5′-3′-, and middle portions of the these genes, that hybridize similarly to a probe array and that produce the most consistently linear curve of hybridization signal over a range of normalization control gene segment concentrations. These methods have applicability across a broad spectrum of hybridization formats.