重组12号染色体开放阅读框72蛋白
交货期：1周
产品别名：Recombinant ETFBKMT
Recombinant electron transfer flavoprotein subunit beta lysine methyltransferase protein
Recombinant electron transfer flavoprotein subunit beta lysine methyltransferase protein
基因名：
产品别名：
背景信息：
ETFBKMT
产品别名：
C12orf72； ETFB-KMT； METTL20； ETFBKMT； electron transfer flavoprotein subunit beta lysine methyltransferase； electron transfer flavoprotein subunit beta lysine methyltransferase； electron transfer flavoprotein beta subunit lysine methyltransferase； ETFB lysine methyltransferase； methyltransferase like 20； methyltransferase-like protein 20； protein N-lysine methyltransferase METTL20； 12号染色体开放阅读框72；
背景信息：
GTPase-activating proteins (GAPs) accelerate the intrinsic rate of GTP hydrolysis of Ras-related proteins, resulting in downregulation of their active form. ARHGAP36 (Rho GTPase activating protein 36) is a 547 amino acid protein that contains one Rho-GAP domain. Conserved in chimpanzee, dog, cow, mouse and rat, ARHGAP36 exists as five alternatively spliced isoforms and is encoded by a gene that maps to human chromosome Xq26.1. Chromosome X consists of nearly 153 million base pairs encoding approximately 1,000 genes. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are X chromosome-linked conditions that affect males more frequently because males carry a single X chromosome.
产品发布日期：2026.05.06
广州伟伯科技有限公司