DYM Rabbit Polyclonal Antibody, 100ul Cell fragmentation and collection Most MS4A genes| including MS4A10|

Most MS4A genes| including MS4A10| encode proteins with at least 4 potential transmembrane domains and N- and C-terminal cytoplasmic domains encoded by distinct exons

induction:Detected at low levels at interphase and in resting cells

The protein mediates cellular binding to particles and immune complexes that have activated complement

Terminates the action of GABA by its high affinity sodium-dependent reuptake into presynaptic terminals

Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6

DYM Rabbit Polyclonal Antibody, 100ul Cell fragmentation and collection Most MS4A genes| including MS4A10|This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia Dyggve Melchior Clausen (DMC) dysplasia and Smith McCort (SMC) dysplasia which involve both skeletal defects and mental retardation.