Analytical Data
-
Gene name
plsC
- Application
-
Alternative Names
plsC；DAPAT；DHAPAT；Dihydroxyacetone phosphate acyltransferase
-
Species
E.coli
-
Source
E. coli
-
Tag
His tag N-Terminus
-
Purity
Greater than 90% as determined by SDS-PAGE.
-
Uniprot
P26647
-
Expression Region
1-245aa
-
AA Sequence
MLYIFRLIITVIYSILVCVFGSIYCLFSPRNPKHVATFGHMFGRLAPLFGLKVECRKPTDAESYGNAIYIANHQNNYDMVTASNIVQPPTVTVGKKSLLWIPFFGQLYWLTGNLLIDRNNRTKAHGTIAEVVNHFKKRRISIWMFPEGTRSRGRGLLPFKTGAFHAAIAAGVPIIPVCVSTTSNKINLNRLHNGLVIVEMLPPIDVSQYGKDQVRELAAHCRSIMEQKIAELDKEVAEREAAGKV
-
Molecular Weight
29.5 kDa
-
Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
-
Form
Freeze-dried powder
-
Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
-
Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
-
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.
-
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.
-
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
The study of the Pseudomonas syringae pv. syringae (Pss) pathogenicity factor PLSC (Pseudomonas syringae locus C) recombinant protein has gained significant attention within the field of plant pathology and biochemistry. PLSC plays a crucial role in the bacterium’s interactions with host plants, particularly in the modulation of plant immune responses. Understanding PLSC's mechanism of action is vital for developing effective strategies to combat plant diseases caused by Pseudomonas syringae, which represents a serious threat to various crop species worldwide. Recent advances in recombinant DNA technology have enabled the cloning and expression of the PLSC gene in suitable host systems, allowing for the production of functional recombinant PLSC protein. Studies have focused on characterizing the biochemical properties of this protein and elucidating its role in pathogenicity, including its interactions with plant host receptors and signaling pathways. Additionally, the PLSC protein may serve as a potential target for developing novel biopesticides or resistance gene pyramiding in crop breeding programs. Overall, research into PLSC recombinant protein is pivotal not only for enhancing our understanding of plant-pathogen interactions but also for contributing to sustainable agricultural practices by mitigating the impact of bacterial plant diseases.
