蛋白质/抗原/多肽 >> 重组蛋白
重组DENND4A蛋白
产品介绍 基因名: DENND4A 产品别名: IRLB; MYCPBP; DENND4A; DENN domain containing 4A; DENN domain containing 4A; C-myc promoter-binding protein; DENN domain-containing protein 4A; DENN/MADD domain containing 4A; c-myc promoter binding protein; DENND4A蛋白; 背景信息: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. 标签:His-tag |
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