Analytical Data
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Gene name
PRELID1
- Application
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Alternative Names
PRELID1
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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
Q9Y255
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Expression Region
36-219 aa
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AA Sequence
TEDIVHREVTPDQKLLSRRLLTKTNRMPRWAERLFPANVAHSVYVLEDSIVDPQNQTMTTFTWNINHARLMVVEERCVYCVNSDNSGWTEIRREAWVSSSLFGVSRAVQEFGLARFKSNVTKTMKGFEYILAKLQGEAPSKTLVETAKEAKEKAKETALAATEKAKDLASKAATKKQQQQQQFV
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Molecular Weight
33.9 kDa
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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
Related Products
Protein Description
PRELID1, or PRELI domain-containing 1, is a protein implicated in various cellular processes, particularly in mitochondrial function and lipid metabolism. Its role in the regulation of lipid droplet formation and interaction with mitochondrial membranes has garnered interest in the context of metabolic disorders and mitochondrial diseases. Recent studies have identified PRELID1’s involvement in autophagy and its potential impact on energy homeostasis, linking it to cellular stress responses and homeostasis. The understanding of PRELID1’s functions is critical for deciphering the underlying mechanisms of diseases characterized by mitochondrial dysfunction, including neurodegenerative conditions. The recombinant expression and purification of PRELID1 have become essential for elucidating its biochemical properties and interactions with other cellular components. Investigating the structure and function of PRELID1 can provide insights into its potential as a therapeutic target for metabolic diseases and enhance our understanding of mitochondrial biology. Overall, the research surrounding PRELID1 aims to bridge the gaps in knowledge regarding its role in cellular metabolism and disease, underscoring its significance in both fundamental biology and potential clinical applications.
