Analytical Data
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Gene name
MYH4
- Application
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Alternative Names
MYH4；Myosin-4
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Species
Human
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Source
E. coli
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Tag
His tag N-Terminus
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q9Y623
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Expression Region
全长
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AA Sequence
full
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
MYH4 is a member of the myosin gene family, specifically encoding a heavy chain that is predominantly expressed in fast-twitch muscle fibers. This protein plays a critical role in muscle contraction and energy metabolism, making it fundamental to understanding muscle physiology and related disorders. Research has shown that alterations in MYH4 expression can impact muscle performance and contribute to various conditions, such as muscular dystrophies and age-related muscle loss. The recombinant MYH4 protein is increasingly being studied for its potential applications in regenerative medicine and biotechnology, particularly in muscle repair and performance enhancement. Additionally, investigating MYH4's structure and function can provide insights into the molecular mechanisms underlying muscle diseases and help in the development of targeted therapies. Through techniques such as gene cloning, protein expression, and functional assays, researchers aim to elucidate the role of MYH4 in muscle mechanics and its potential as a therapeutic target, highlighting its significance in both basic and applied biomedical research.
