Analytical Data
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Gene name
CFDP1
- Application
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Alternative Names
Bucentaur
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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
Q9UEE9
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Expression Region
1-299aa
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Molecular Weight
60.6 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
CFDP1 (Ciliated Flagellar Defective Protein 1) is a crucial protein that has garnered significant attention in the field of molecular biology and cell biology due to its role in ciliary function and cellular signaling. Cilia are essential cellular structures that play vital roles in cell motility and sensory functions. Mutations or dysfunctions in ciliary proteins, such as CFDP1, are associated with a range of genetic disorders, collectively known as ciliopathies, which can lead to severe developmental and health issues. The study of CFDP1, particularly through the recombinant expression of the protein, is pivotal for understanding its structural and functional properties. This research aims to elucidate the molecular mechanisms by which CFDP1 influences ciliary formation and function, which may provide insights into its role in diseases linked to ciliary dysfunction. Recombinant CFDP1 protein can be utilized in various biochemical assays to investigate its interactions with other ciliary proteins and cellular components, contributing to our understanding of ciliary dynamics. Additionally, understanding the role of CFDP1 in developmental processes can have implications for therapeutic strategies targeting ciliopathies. Overall, research into CFDP1 not only contributes to the basic understanding of ciliary biology but also holds potential for developing clinical applications aimed at treating diseases caused by ciliary malfunctions.
