NCBI and Uniprot Product Information
NCBI Description
predominant myosin light chain in cardiac tissue [RGD, Feb 2006]
Uniprot Description
MYL3: Regulatory light chain of myosin. Does not bind calcium. Defects in MYL3 are the cause of familial hypertrophic cardiomyopathy type 8 (CMH8). Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. CMH8 inheritance can be autosomal dominant or recessive.
Protein type: Motor; Motility/polarity/chemotaxis
Cellular Component: A band; I band; myosin complex
Molecular Function: actin monomer binding; calcium ion binding; motor activity
Biological Process: cardiac muscle contraction; muscle contraction; regulation of striated muscle contraction; regulation of the force of heart contraction; skeletal muscle development; ventricular cardiac muscle morphogenesis
Research Articles on Myl3
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Product Notes
The Rat Myl3 myl3 (Catalog #AAA288414) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA288414 ELISA Kit recognizes Rat Myl3. It is sometimes possible for the material contained within the vial of "Myosin light chain 3, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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