寡核苷酸阵列比较基因组杂交标记试剂盒 CGH labeling kit for oligo arrays
CGH labeling kit for oligo arrays ENZ-42671
寡核苷酸阵列比较基因组杂交标记试剂盒
产品特点：
无需扩增或降低复杂度，能够实现整个基因组DNA分析；
能够为各种复杂的异质样品提供良好的动态分析检测范围
QC基准经高分辨度分析验证
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货号 |
产品名称 |
规格 |
品牌 |
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ENZ-42671-K010 |
CGH labeling kit for oligo arrays |
20 reactions |
ENZO(美国) |
|
ENZ-42671-K010 |
CGH labeling kit for oligo arrays |
200 reactions |
ENZO(美国) |
文献引用：
First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children: D.N. Senanayake, et al.; Mol. Gen. Met. Rep. 2, 81 (2015), Application(s): DNA Labeling,
A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings: J.W. Ahn, et al.; Peer J. 2, e354 (2014), Application(s): Labeling of DNA extracted from chorionic villi and amniotic fluid samples, Abstract; Full Text
Analysis of MYB oncogene in transformed adenoid cystic carcinomas reveals distinct pathways of tumor progression: A.F. Costa, et al.; Lab. Invest. 94, 692 (2014), Abstract;
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association: J. Winberg, et al.; PLoS One 9, 85313 (2014), Abstract; Full Text
Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: Further delineation of an emerging syndrome: M. Cafferkey, et. al.; Am. J. Med. Genet. A. Epub ahead of print, (2014), Abstract;
An improved method to extract DNA from 1ml of uncultured amniotic fluid from patients at less than 16 weeks’ gestation: A.L. Mosca-Boidron, et al.; PLoS One 8, e59956 (2013), Abstract; Full Text
Chromosome 20p11 gains are associated with liver-specific metastasis in patients with colorectal cancer: L.J. Mekenkamp, et al.; Gut 62, 94 (2013), Abstract;
DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas: M.M. Kamieniak, et al.; Br. J. Cancer 108, 1732 (2013), Abstract; Full Text
Focal aberrations indicate EYA2 and hsa‐miR‐375 as oncogene and tumor suppressor in cervical carcinogenesis: M. Bierkens, et al.; Genes Chromosomes Cancer 52, 56 (2013), Abstract;
Germline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumours: J. Aury-Landas, et al.; Eur. J. Hum. Genet. 21, 1369 (2013), Abstract;
Intellectual disability and hemizygous GPD2 mutation: D.Q. Barge-Schaapveld, et al.; Am. J. Med. Genet. A. 161A, 1044 (2013), Abstract;
Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders: M. Tropeano, et al.; PLoS One 8, e61365 (2013), Application(s): Blood samples from patients with neurodevelopmental disorders, Abstract; Full Text
UE-S601122S/S601122M/S601122L 
