重组5号染色体开放阅读框51蛋白
交货期：1周
产品别名：Recombinant Rimoc1
Recombinant RAB7A interacting MON1-CCZ1 complex subunit 1 protein
Recombinant RAB7A interacting MON1-CCZ1 complex subunit 1 protein
基因名：
产品别名：
背景信息：
Rimoc1
产品别名：
AI195826； AW549877； Rimoc1； RAB7A interacting MON1-CCZ1 complex subunit 1； RAB7A interacting MON1-CCZ1 complex subunit 1； RAB7A-interacting MON1-CCZ1 complex subunit 1； UPF0600 protein C5orf51 homolog； 5号染色体开放阅读框51；
背景信息：
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The LOC285636 gene product has been provisionally designated LOC285636 pending further characterization.
产品发布日期：2026.03.18
广州伟伯科技有限公司