Analytical Data
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Gene name
bcsP31
- Application
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Species
Brucella melitensis biotype 1
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Source
E. coli
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Tag
N- His & C- Myc
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
P0A3T2
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Expression Region
29-329aa
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Molecular Weight
39.0 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
The bcsP31 protein, an essential component in the biosynthesis of bacterial cellulose, has garnered significant attention in microbial biotechnology due to its potential applications in various fields, including biomedicine, materials science, and environmental sustainability. As a member of the cellulose synthase complex, bcsP31 plays a crucial role in the polymerization of glucose units into cellulose fibers, which are known for their strength and biocompatibility. The study of bcsP31 is pivotal for understanding the intricate mechanisms of cellulose production in bacteria, particularly in organisms such as *Gluconacetobacter xylinus*, which are renowned for their ability to produce high-quality cellulose. Researchers are particularly interested in the protein’s structure, function, and regulatory mechanisms, as these factors influence the efficiency of cellulose synthesis. Advances in genetic engineering and recombinant protein expression have enabled the production of bcsP31 in various host systems, facilitating detailed studies on its characteristics and interactions with other components of the cellulose synthesis machinery. Moreover, the insights gained from bcsP31 research can lead to innovative strategies for enhancing cellulose production, enabling its use in bio-based materials, sustainable packaging, and advanced drug delivery systems. In summary, the ongoing investigation into bcsP31 and its associated pathways holds the promise of unlocking new biotechnological applications and addressing environmental challenges through the utilization of microbial cellulose.











