Human A disintegrin and metalloproteinase with thrombospondin motifs 18(ADAMTS18) ELISA kit
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中文名称:人金属肽酶含血小板反应蛋白18(ADAMTS18)酶联免疫试剂盒
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货号:CSB-EL001306HU
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规格:96T/48T
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价格:¥3600/¥2500
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其他:
产品详情
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产品描述:人金属肽酶含血小板反应蛋白18(ADAMTS18)酶联免疫试剂盒(CSB-EL001306HU)为双抗夹心法ELISA试剂盒,定量检测血清、血浆、组织匀浆样本中的ADAMTS18含量。ADAMTS18属于ADAMTS蛋白酶家族,参与细胞外基质的代谢和组织重塑。研究表明,它在多种生理和病理过程中发挥作用,如血管生成、肿瘤进展等。其机制可能涉及对特定底物的蛋白水解切割,不过关于它的确切功能和作用机制仍在进一步研究中。试剂盒检测范围为0.016ug/ml- 10ug/ml,支持科研领域对ADAMTS18蛋白表达的定量分析,适用于癌症生物学研究、组织微环境调控、胚胎发育或疾病模型构建等方向,为探索ADAMTS18在细胞迁移、血管形成或肿瘤转移中的作用机制提供可靠工具本品仅用于科研,不用于临床诊断,产品具体参数及操作步骤详见产品说明书。
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别名:ADAMTS18 ELISA kit; ADAMTS21A disintegrin and metalloproteinase with thrombospondin motifs 18 ELISA kit; ADAM-TS 18 ELISA kit; ADAM-TS18 ELISA kit; ADAMTS-18 ELISA kit; EC 3.4.24.- ELISA kit
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缩写:
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Uniprot No.:
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种属:Homo sapiens (Human)
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样本类型:serum, plasma, tissue homogenates
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检测范围:0.016ug/ml- 10ug/ml
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灵敏度:0.016ug/ml
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反应时间:1-5h
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样本体积:50-100ul
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检测波长:450 nm
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研究领域:Cell Biology
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测定原理:quantitative
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测定方法:Sandwich
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数据处理:
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货期:3-5 working days
相关产品
靶点详情
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基因功能参考文献:
- In summary, we demonstrate that ADAMTS18 silencing in breast cancer is significantly correlated with promoter CpG methylation. ADAMTS18 acts as an antagonist of AKT and NF-kappaB signaling, further suppressing EMT and metastasis of breast cancer cells. PMID: 28503860
- This study showed that ADAMTS1, 8, and 18 are highly expressed in GC and its nodal metastases, suggesting important roles of these proteases in carcinogenesis and lymphatic metastasis. The findings from the present study indicate that these proteases may be promising candidates for novel and alternative treatments in GC (gastric cancer) PMID: 28814085
- Studies suggest that ADAM metallopeptidase with thrombospondin type 1 motif, 18 protein (ADAMTS-18) as a promising diagnostic and therapeutic target. PMID: 24896365
- Novel homozygous mutations in ADAMTS18 were identified, consisting of c.1067T>A [p.L356*] in the first proband, c.2159G>C [p.C720S] in the 2 affected brothers PMID: 24874986
- Results suggest that ADAMTS18 plays an essential role in early eye development and that mutations therein cause a distinct eye phenotype that is mainly characterized by microcornea and myopia. PMID: 23818446
- study reveals that mutations in the ADAMTS18 gene can cause a broad phenotypic spectrum of eye disorders and contribute to shed further light on the complexity of retinal diseases PMID: 23356391
- the study identified ADAMTS18 as the only gene carrying a homozygous protein altering mutation. PMID: 21862674
- ADAMTS18 mutations promote growth, migration, and metastasis in melanoma PMID: 21047771
- ADAMTS18 gene methylation in 3 types of cancers was significantly higher than normal tissues. No significant association was found between methylation status & TNM staging. Epigenetic regulation of ADAMTS18 was associated with carcinogenesis. PMID: 19806480
- Functional epigenetics show ADAMTS18 to be a novel functional tumor suppressor, being frequently inactivated epigenetically in multiple carcinomas. PMID: 17546048
- ADAMTS18 and TGFBR3 might underlie BMD determination in the major human ethnic groups. PMID: 19249006
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相关疾病:Microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT)
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亚细胞定位:Secreted, extracellular space, extracellular matrix.
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组织特异性:Expressed in fetal lung, liver, and kidney and in adult brain, prostate, submaxillary gland, and endothelium.
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数据库链接:
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