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    • 3. 发明公开
    • Methods for identifying synovium cells having decreased proliferative or chondrogenic potentials
    • 识别具有降解的增殖或变性潜能的概念细胞的方法
    • KR20100037581A
    • 2010-04-09
    • KR20100018725
    • 2010-03-02
    • SEOUL NAT UNIV IND FOUNDATION
    • HAN HYUK SOOLEE SAHNG HOONLEE MYUNG CHUL
    • C12Q1/68C12N5/077C12N15/12
    • C12Q1/6883C12N5/0655G01N2800/10
    • PURPOSE: A kit for identifying or detecting synovial membrane cells with reduced proliferation or chondroplasia ability is provided to easily and accurately identify chodrocytes and treat injury of joint cartilage. CONSTITUTION: A kit for identifying or detecting synovial membrane cells with reduced proliferation or chondroplasia ability contains a primer or probe which specifically binds to cyclin-dependent kinase inhibitor 2A gene, v-Ki-ras 2 gene, thrombospondin 1 gene, mitogen-activated protein kinase 9 gene, ecto-nucleotide pyrophosphatase/phosphodiesterase 1 gene, tumor necrosis factor receptor superfamily member 6 gene, tumor necrosis factor receptor superfamily member 10d gene, tumor necrosis receptor superfamily member 10b gene, tumor necrosis factor receptor superfamily 11b gene, TNF receptor-related factor 4 gene or PRKC apoptosis WT1 regulator(PAWR) gene sequence. A method for identifying or detecting synovial membrane cells with reduced proliferation or chondroplasia ability comprises: a step of collecting total RNA from synovial membrane cells; a step of constructing cDNA from the total RNA; a step of hybridizing the cDNA with specific probe; or a step of detecting hybridization, a step of amplifying cDNA using specific primer; and a step of confirming amplified product.
    • 目的:提供一种用于鉴定或检测减少增殖或软骨发育能力的滑膜细胞的试剂盒,用于容易且准确地鉴定切割细胞并治疗关节软骨的损伤。 构成:用于鉴定或检测减少增殖或软骨发育能力的滑膜细胞的试剂盒含有特异性结合细胞周期蛋白依赖性激酶抑制剂2A基因,v-Ki-ras 2基因,血小板反应蛋白1基因,促分裂原活化蛋白的引物或探针 激酶9基因,异位核苷酸焦磷酸酶/磷酸二酯酶1基因,肿瘤坏死因子受体超家族成员6基因,肿瘤坏死因子受体超家族成员10d基因,肿瘤坏死因子超家族成员10b基因,肿瘤坏死因子受体超家族11b基因, 相关因子4基因或PRKC凋亡WT1调节因子(PAWR)基因序列。 用于鉴定或检测具有降低的增殖或软骨发育能力的滑膜细胞的方法包括:从滑膜细胞收集总RNA的步骤; 从总RNA构建cDNA的步骤; cDNA与特异性探针杂交的步骤; 或检测杂交的步骤,使用特异性引物扩增cDNA的步骤; 以及确认扩增产物的步骤。
    • 4. 发明公开
    • ANKH의 신규 돌연변이
    • 在ANKH的新的突变
    • KR1020070097236A
    • 2007-10-04
    • KR1020060028164
    • 2006-03-29
    • 경북대학교 산학협력단
    • 최제용김효진
    • C07K14/47
    • C07K14/705C07K16/28G01N33/6893G01N2333/705G01N2800/10
    • A novel mutant of ANKH(human homolog of ANK(ankylosis)) is provided to diagnose and identify craniometaphyseal dysplasia(CMD) and perform genetic study for the disease. A mutant protein of ANKH has the amino acid sequence of SEQ ID NO:2 and comprises mutation, in which 290th-295th amino acids of wild ANKH, "Tyr-Gly-Trp-Leu-Thr-Glu" are substituted by "Gln-Gly"; and the mutation is missense mutation . A nucleic acid molecule encoding the mutant protein of ANKH has the nucleotide sequence of SEQ ID NO:1. An expression vector contains the ANKH mutant nucleic acid molecule. An antibody specifically binding to the mutant of ANKH is provided. A genetic marker useful for diagnosis of craniometaphyseal dysplasia(CMD) comprises 10-100 consecutive residues containing 1188th-1193rd nucleotides in the nucleotide sequence of SEQ ID NO:1.
    • 提供ANKH(ANK(强直性)的人类同源物)的新型突变体,用于诊断和鉴定颅髓发育不良(CMD)并进行该疾病的遗传学研究。 ANKH的突变蛋白具有SEQ ID NO:2的氨基酸序列,并且包含突变,其中野生型ANKH“Tyr-Gly-Trp-Leu-Thr-Glu”的第290〜295位氨基酸被“Gln- 甘氨酸“; 突变是错义突变。 编码ANKH突变蛋白的核酸分子具有SEQ ID NO:1的核苷酸序列。 表达载体含有ANKH突变核酸分子。 提供了与ANKH突变体特异性结合的抗体。 可用于诊断颅脑膜发育不良(CMD)的遗传标记包含在SEQ ID NO:1的核苷酸序列中含有1188位至第1193位核苷酸的10-100个连续残基。