重组FCHSD1蛋白
交货期：1周
产品别名：Recombinant FCHSD1
Recombinant FCH and double SH3 domains 1 protein
Recombinant FCH and double SH3 domains 1 protein
基因名：
产品别名：
背景信息：
FCHSD1
产品别名：
NWK2； FCHSD1； FCH and double SH3 domains 1； FCH and double SH3 domains 1； F-BAR and double SH3 domains protein 1； FCH and double SH3 domains protein 1； nervous wreck homolog 2； protein nervous wreck 2； FCHSD1蛋白；
背景信息：
FCHSD1 is a 690 amino acid protein that contains one FCH domain and two SH3 domains. FCHSD1 exists as three isoforms as a result of alternative splicing events. The gene encoding FCHSD1 maps to chromosome 5, which 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.
产品发布日期：2026.01.27
广州伟伯科技有限公司