PRIO Polyclonal Antibody, 20ul NGS Oligos Mutations in this gene are

Mutations in this gene are associated with autosomal recessive nonsyndromic deafness (DFNB82)

induction:Activity in polarized intestinal cells is regulated by the association between SLC3A2/4F2 (in the SLC3A2/4F2-LAT2 heterodimer) and ICAM1

stable surface processes ensure an optimal culture environment for high-yield cell cultures

The encoded protein contains domains involved in DNA binding

the AMME complex (Alport syndrome

PRIO Polyclonal Antibody, 20ul NGS Oligos Mutations in this gene areThe protein encoded by this gene is a membrane glycosylphosphatidylinositol anchored glycoprotein that tends to aggregate into rod like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as