PBFE Polyclonal Antibody, 20ul Oligo Pool the calmodulin-like calcium-binding domain

the calmodulin-like calcium-binding domain

Mutations in this gene cause Schwartz-Jampel syndrome type 2

Don't compromise quality - trust in natural color and non-sterile design

also known as inherited thrombophilia

MYB encodes a protein with three HTH DNA-binding domains that functions as a transcription regulator

PBFE Polyclonal Antibody, 20ul Oligo Pool the calmodulin-like calcium-binding domainEnoyl CoA hydratase and 3 hydroxyacyl CoA dehydrogenase by EHHADH is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta oxidation pathway. The N terminal region of the encoded protein contains enoyl CoA hydratase activity while the C terminal region contains 3 hydroxyacyl CoA dehydrogenase activity. Defects in EHHADH are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different