MTCH2 Rabbit Polyclonal Antibody, 100ul Plasma Mutations in PKD2 are associated

Mutations in PKD2 are associated with autosomal dominant polycystic kidney disease type 2

a disease resulting in hemolytic anemia and thrombosis

• Dual protection housing particularly benefit for safe running

Alternative splicing of this gene results in two products

MTCH2 Rabbit Polyclonal Antibody, 100ul Plasma Mutations in PKD2 are associatedThis gene encodes a member of the SLC25 family of nuclear encoded transporters that are localized in the inner mitochondrial membrane. Members of this superfamily are involved in many metabolic pathways and cell functions. Genome wide association studies in human have identified single nucleotide polymorphisms in several loci associated with obesity. This gene is one such locus which is highly expressed in white adipose tissue and adipocytes and