FBX46 Rabbit Polyclonal Antibody, 100ul Molecular Biology Defects in PEX7 cause peroxisome

Defects in PEX7 cause peroxisome biogenesis disorders (PBDs)

Mitogen-activated protein kinase kinase kinase MLK4 is a negative regulator of TLR4 signaling

It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome

This gene encodes the smallest subunit of DNA polymerase delta

The GAL4 protein of Saccharomyces cerevisiae is one of the most thoroughly characterized transcriptional activators

FBX46 Rabbit Polyclonal Antibody, 100ul Molecular Biology Defects in PEX7 cause peroxisomeMembers of the F box protein family such as FBXO46 are characterized by an approximately 40 amino acid F box motif. SCF complexes formed by SKP1 (MIM 601434) cullin (see CUL1; MIM 603134) and F box proteins act as protein ubiquitin ligases. F box proteins interact with SKP1 through the F box and they interact with ubiquitination targets through other protein interaction domains (Jin et al. 2004