KBTBA Rabbit Polyclonal Antibody, 50ul Peripheral Blood Separation Tube This gene encodes a member

This gene encodes a member of the thioredoxin family of enzymes

Reg family members REG1B

Mutations in this gene have been found in individuals with nephrotic syndrome

which is a characteristic pattern of nuclear movement in neural progenitors

in intralumenal endosomal vesicle formation

KBTBA Rabbit Polyclonal Antibody, 50ul Peripheral Blood Separation Tube This gene encodes a memberThis gene is a member of the kelch like family. The encoded protein contains a BACK domain a BTB POZ domain and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM) a rare congenital muscle disorder.