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Responsible for the dehydration step in very long-chain fatty acids (VLCFAs) synthesis (By similarity). Additionally we are shipping Protein Tyrosine Phosphatase-Like (Proline Instead of Catalytic Arginine), Member B Antibodies (20) and many more products for this protein.
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Mutations in HACD1 can result in myopathies in humans; knockout mice lacking Hacd1 develop myopathic phenotypes. Data (including data from studies using knockout mice and cultured cells from knockout mice) suggest that HACD1 and HACD2 exhibit overlapping substrate specificities and thus appear to represent redundant activities in skeletal muscle.
Data describe a novel human member of the protein tyrosine phosphatase (show ACP1 Proteins)-like B (PTPLB) family, an integral protein of the endoplasmic reticulum membrane, as a BAP31 (show BCAP31 Proteins)-interacting protein.
Responsible for the dehydration step in very long-chain fatty acids (VLCFAs) synthesis (By similarity).
3-hydroxyacyl-CoA dehydratase 2
, protein-tyrosine phosphatase-like member B
, very-long-chain (3R)-3-hydroxyacyl-[acyl-carrier protein] dehydratase 2
, Protein-tyrosine phosphatase-like member B