TM1L1 Polyclonal Antibody, 20ul Filtration and cell motility

and cell motility

C1QC encodes the C-chain polypeptide of human complement subcomponent C1q

Mutations in this gene or in the enhancer regions can cause ocular disorders such as aniridia and Peter's anomaly

as well as non-voltage gated sodium channels

FXYD4 (CHIF)

TM1L1 Polyclonal Antibody, 20ul Filtration and cell motilityProbable adapter protein involved in signaling pathways. Interacts with the SH2 and SH3 domains of various signaling proteins when it is phosphorylated. May promotes FYN activation, possibly by disrupting intramolecular SH3 dependent interactions.,PTM: Phosphorylated on tyrosines by FYN (By similarity). Phosphorylated upon DNA damage, probably by ATM or ATR.,Belongs to the TOM1 family.,Contains 1 GAT domain.,Contains 1 VHS domain.,subunit: Interacts