Analytical Data
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Gene name
DHDDS
- Application
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Alternative Names
Cis-isoprenyltransferase
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Species
Human
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Source
E. coli
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Tag
N- GST
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q86SQ9
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Expression Region
1-333aa
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Molecular Weight
65.7 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
DHDDS (Dihydroceramide Desaturase) is an essential enzyme involved in sphingolipid metabolism, specifically in the synthesis of unsaturated fatty acids from saturated precursors. It plays a crucial role in the formation of ceramide, a key component of cellular membranes that influences various physiological processes, including cell signaling, apoptosis, and stress responses. Dysregulation of DHDDS activity has been implicated in several diseases, including cancer, neurodegenerative disorders, and metabolic syndrome, highlighting its potential as a therapeutic target. The recombinant production of DHDDS allows for detailed structural and functional studies, facilitating the understanding of its enzymatic mechanisms and substrate specificity. Moreover, recombinant DHDDS can be used to explore its interactions with various ligands and inhibitors, paving the way for developing novel pharmacological agents. Advances in biotechnological methods, such as genetic engineering and protein purification techniques, have significantly enhanced the ability to produce high yields of functional DHDDS, which is vital for both basic research and drug development. By elucidating the structure-function relationship of DHDDS through recombinant protein studies, researchers aim to uncover new insights into the regulatory mechanisms governing lipid metabolism and its implications in health and disease. This line of research holds promise for harnessing DHDDS as a biomarker or target in therapeutic strategies, potentially leading to innovative treatments for conditions associated with sphingolipid dysregulation.











