ApoL5 Polyclonal Antibody, 20ul Buffers & Solutions may modify the adrenoleukodystrophy phenotype

may modify the adrenoleukodystrophy phenotype

Polymorphisms resulting in amino acid substitutions in these two subunits have been associated with the regulation of blood pressure in an animal model of hypertension

and faintly in placenta

The product of ALDH1A2 (aldehyde dehydrogenase 1 family member A2) is an enzyme that catalyzes the synthesis of retinoic acid (RA) from retinaldehyde

Two transcript variants resulting from alternative splicing have been identified

ApoL5 Polyclonal Antibody, 20ul Buffers & Solutions may modify the adrenoleukodystrophy phenotypeAPOL5 (apolipoprotein L5) is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles.