Analytical Data
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Gene name
AP4m1
- Application
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Alternative Names
Mu-Adaptin-Related Protein-2; AP-4 Adapter Complex Mu Subunit; Adaptor-Related Protein Complex AP-4 Mu4 Subunit
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Species
Mouse
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Source
E. coli
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Tag
N-His
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q9JKC7
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Expression Region
Met1~Val208
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Molecular Weight
25kDa
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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
The AP4M1 protein, a member of the AP (adaptor protein) family, plays a crucial role in intracellular trafficking, particularly in the formation of transport vesicles that facilitate the movement of proteins and lipids between cellular compartments. Recent studies have highlighted its involvement in the secretory pathway, endocytosis, and the maintenance of cellular homeostasis. AP4M1 is particularly interesting due to its association with various physiological processes and its potential implications in disease mechanisms, including neurodegenerative disorders and certain cancers. Genetic mutations or dysregulation of AP4M1 have been linked to impaired cellular transport functions, which can lead to pathological conditions. As research progresses, understanding the precise functions and regulatory mechanisms of AP4M1 can provide insights into its role in health and disease, paving the way for targeted therapeutic strategies. The exploration of AP4M1 as a recombinant protein offers opportunities for investigating its structure-function relationships and interactions with other cellular components, further elucidating its impact on cellular dynamics and disease pathology.
