LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification Isoforms Ialpha and Ibeta have

Isoforms Ialpha and Ibeta have identical cGMP-bindin

but their existence has not been verified

which can be easily removed layer by layer

SRY-related HMG-box (SOX) genes encode a family of DNA-binding proteins containing a 79-amino acid HMG (high mobility group) domain that shares at least 50% sequence identity with the DNA-binding HMG box of the SRY protein (MIM 480000)

The type II isozyme

LETM1 Rabbit Polyclonal Antibody, 50ul Peptide Modification Isoforms Ialpha and Ibeta haveThis gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf Hirschhorn syndrome a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8 15 and 19.