Analytical Data
-
Gene name
PSKR
- Application
-
Alternative Names
(DcPSKR1)(Phytosulfokine LRR receptor kinase 1)
-
Species
Daucus carota
-
Source
Yeast
-
Tag
C- His
-
Purity
Greater than 90% as determined by SDS-PAGE.
-
Uniprot
Q8LPB4
-
Expression Region
24-659aa
-
Molecular Weight
70.8 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
Pseudomonas syringae is a well-known plant pathogenic bacterium that employs various strategies to infect host plants, including the secretion of effector proteins to manipulate host immune responses. Among these effector proteins, the PSKR (Pseudomonas Syringae Kinase Regulator) plays a pivotal role in modulating host signaling pathways during infection. Research on PSKR has gained attention due to its potential implications in understanding plant-pathogen interactions and developing disease-resistant plant varieties. The study of PSKR involves elucidating its structure, function, and mechanisms of action at the molecular level, which is crucial for comprehending how P. syringae evades plant defenses. Furthermore, the reconstitution of PSKR as a recombinant protein allows researchers to assess its activity and interactions with host proteins, providing insights into the biochemical pathways that underlie pathogenicity. Advances in techniques such as structural biology and biochemistry have significantly contributed to elucidating the role of PSKR in virulence. This research not only enhances our fundamental understanding of plant-microbe interactions but also opens avenues for agricultural applications, including biotechnological approaches for enhancing crop resistance against bacterial infections.
