Analytical Data
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Gene name
MIPOL1
- Application
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Alternative Names
MIPOL1Mirror-image polydactyly gene 1 protein
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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
Q8TD10
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Expression Region
1-442 aa
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AA Sequence
MENWSKDITH SYLEQETTGI NKSTQPDEQL TMNSEKSMHR KSTELVNEIT CENTEWPGQR STNFQIISSY PDDESVYCTT EKYNVMEHRH NDMHYECMTP CQVTSDSDKE KTIAFLLKEL DILRTSNKKL QQKLAKEDKE QRKLKFKLEL QEKETEAKIA EKTAALVEEV YFAQKERDEA VMSRLQLAIE ERDEAIARAK HMEMSLKVLE NINPEENDMT LQELLNRINN ADTGIAIQKN GAIIVDRIYK TKECKMRITA EEMSALIEER DAALSKCKRL EQELHHVKEQ NQTSANNMRH LTAENNQERA LKAKLLSMQQ ARETAVQQYK KLEEEIQTLR VYYSLHKSLS QEENLKDQFN YTLSTYEEAL KNRENIVSIT QQQNEELATQ LQQALTERAN MELQLQHARE ASQVANEKVQ KLERLVDVLR KKVGTGTMRT VI
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Molecular Weight
51.5 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
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Protein Description
MIPOL1, or "Mitochondrial protein involved in oxidative phosphorylation 1," is a protein of significant interest in cellular biology and mitochondrial research. It plays a critical role in maintaining mitochondrial function and dynamics, which are essential for energy production through ATP synthesis. Mitochondrial dysfunction is implicated in various diseases, including neurodegenerative disorders, cardiovascular diseases, and metabolic syndromes. Recent studies have suggested that MIPOL1 is involved in the regulation of mitochondrial morphology, facilitating the balance between mitochondrial fission and fusion. Such processes are crucial for mitochondrial health and cellular metabolism. Researchers have been investigating the functional pathways of MIPOL1, delving into its potential mechanisms of action in modulating mitochondrial dynamics and how it interacts with other key proteins involved in these processes. Furthermore, understanding the role of MIPOL1 could illuminate novel therapeutic targets for diseases characterized by mitochondrial abnormalities. Thus, the recombinant study of MIPOL1 not only enhances our understanding of mitochondrial biology but also paves the way for potential interventions in mitochondrial-linked diseases.
