MRGX4 Polyclonal Antibody, 100ul Site-directed Mutagenesis an autosomal recessive disease in

an autosomal recessive disease in which few or no gamma globulins or antibodies are made

SLC39A1 encodes a member of the zinc-iron permease family

alternative products:Experimental confirmation may be lacking for some isoforms

Isoforms Ialpha and Ibeta have identical cGMP-bindin

The protein (glucosylceramidase beta 3 (gene/pseudogene)) encoded by GBA3 is an enzyme that can hydrolyze several types of glycosides

MRGX4 Polyclonal Antibody, 100ul Site-directed Mutagenesis an autosomal recessive disease inOrphan receptor. Probably involved in the function of nociceptive neurons. May regulate nociceptor function and or development, including the sensation or modulation of pain. Potently activated by enkephalins.