Rtn-3 Monoclonal Antibody, 50ul[BT-MCA1110] Vessels Defects in this gene cause

Defects in this gene cause aortic aneurysm familial thoracic type 6

RUNX1) represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis

CR1 encodes a monomeric single-pass type I membrane glycoprotein found on erythrocytes

xeno-free functional hydrogel for 3D cell culture research

Rtn-3 Monoclonal Antibody, 50ul[BT-MCA1110] Vessels Defects in this gene causeThis gene belongs to the reticulon family of highly conserved genes that are preferentially expressed in neuroendocrine tissues. This family of proteins interact with, and modulate the activity of beta amyloid converting enzyme 1 (BACE1), and the production of amyloid beta. An increase in the expression of any reticulon protein substantially reduces the production of amyloid beta, suggesting that reticulon proteins are negative modulators of BACE1 in