AL1L1 Rabbit Polyclonal Antibody, 20ul Contamination Detection & Removal Defects in this gene are

Defects in this gene are a cause of pulmonary alveolar microlithiasis

Among its related pathways are Metabolism and Amino acid synthesis and interconversion (transamination)

which often serves as a protein-protein interaction domain

cytoskeletal rearrangements and the JNK/SAPK signaling cascade

In several variants

AL1L1 Rabbit Polyclonal Antibody, 20ul Contamination Detection & Removal Defects in this gene areThe protein encoded by this gene catalyzes the conversion of 10 formyltetrahydrofolate, nicotinamide adenine dinucleotide phosphate (NADP+), and water to tetrahydrofolate, NADPH, and carbon dioxide. The encoded protein belongs to the aldehyde dehydrogenase family. Loss of function or expression of this gene is associated with decreased apoptosis, increased cell motility, and cancer progression. There is an antisense transcript that overlaps on the