NR1H2 Polyclonal Antibody, 50ul Cryopreservation Deficiency of this enzyme results

Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome)

Multiple transcript variants encoding different isoforms have been found for HRH4

a group of intracellular lipid receptors

Through obligatory heteromerization

Mammalian mitochondrial complex I is composed of at least 43 different subunits

NR1H2 Polyclonal Antibody, 50ul Cryopreservation Deficiency of this enzyme resultsThe liver X receptors, LXRA (NR1H3; MIM 602423) and LXRB, form a subfamily of the nuclear receptor superfamily and are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. The inducible LXRA is highly expressed in liver, adrenal gland, intestine, adipose tissue, macrophages, lung, and kidney, whereas LXRB is ubiquitously expressed. Ligand activated LXRs form obligate heterodimers