SEMA4A Polyclonal Antibody, 20ul Recombinant Ab Production Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

KCNJ16 may be involved in the regulation of fluid and pH balance

Midline-1 encoded by this MID1 is a member of the tripartite motif (TRIM) family

Angiogenin encoded by ANG is an exceedingly potent mediator of new blood vessel formation

SEMA4A Polyclonal Antibody, 20ul Recombinant Ab Production Defects in TMEM237 are aSEMA4A encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single pass type I membrane protein containing an immunoglobulin like C2 type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for