ELOVL1 Polyclonal Antibody, 50ul Shaker&Mixing Mutations in this gene cause

Mutations in this gene cause lissencephaly 4

MIM 600475) in TFIID

The protein encoded by this gene contains C2H2 zinc finger domains

However| the biological validity and full-length nature of some variants cannot be determined at this time

PPP1R15B encodes a protein phosphatase I-interacting protein that promotes the dephosphorylation of eukaryotic translation initiation factor 2A to regulate translation under conditions of cellular stress

ELOVL1 Polyclonal Antibody, 50ul Shaker&Mixing Mutations in this gene causeElongation of very long chain fatty acid like (ELOVL) proteins 1 6 are members of the ELO family of proteins, which play an important role in tissue specific biosynthesis of very long chain fatty acids and sphingolipids. The ELOVL proteins act as catalysts in fatty acid elongation reduction and localize to the endoplasmic reticulum (ER). Elongation of very long chain fatty acids protein 1 (ELOVL1), also referred to as Ssc1, is the human homolog of the