PFK-C Polyclonal Antibody, 50ul Pipette Holder Mutations in CEP135 are associated

Mutations in CEP135 are associated with autosomal recessive primary microcephaly-8

and acts as a decoy receptor that inhibits the activity of its ligands

Its cytosolic localization was demonstrated by cell fractionation experiments

member 6 (IL1F6)

the encoded protein translocates from the distal tips of the centrioles to the tip of the elongating cilium

PFK-C Polyclonal Antibody, 50ul Pipette Holder Mutations in CEP135 are associatedThe PFKP gene encodes the platelet isoform of phosphofructokinase (PFK) (ATP: D fructose 6 phosphate 1 phosphotransferase, EC 2. . 1). PFK catalyzes the irreversible conversion of fructose 6 phosphate to fructose 1,6 bisphosphate and is a key regulatory enzyme in glycolysis. The PFKP gene, which maps to chromosome 10p, is also expressed in fibroblasts. See also the muscle (PFKM; MIM 610681) and liver (PFKL; MIM 171860) isoforms of phosphofructokinase,