Brn-3 Polyclonal Antibody, 100ul Glassware along with the desmogleins

along with the desmogleins

Defects in PRF1 cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2)

Multiple alternatively splcied transcript variants encoding distinct isoforms have been identified for this gene

Angiomotin mediates angiostatin inhibition of endothelial cell migration and tube formation in vitro

GOSR1 (golgi SNAP receptor complex member 1) encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi and between Golgi compartments

Brn-3 Polyclonal Antibody, 100ul Glassware along with the desmogleinsPOU4F3 (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.