K118197P Anti-FAM9B Polyclonal

The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1，000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. 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 well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The FAM9B gene product has been provisionally designated FAM9B pending further characterization.