Brn-3 Polyclonal Antibody, 20ul Organelle Studies also called triple-A syndrome or

also called triple-A syndrome or Allgrove syndrome

making it perfect for cell culture applications

It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally

YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma) product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins

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Brn-3 Polyclonal Antibody, 20ul Organelle Studies also called triple-A syndrome orPOU4F3 (POU class 4 homeobox 3) encodes a member of the POU domain family of transcription factors. POU domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in POU4F3 are the cause of non syndromic sensorineural deafness autosomal dominant type 15.