Analytical Data
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Gene name
LPPR2
- Application
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Alternative Names
PLPPR2; LPPR2; PRG4; Phospholipid phosphatase-related protein type 2; Lipid phosphate phosphatase-related protein type 2; Plasticity-related gene 4 protein; PRG-4
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Species
Human
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Source
E. coli
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Tag
His tag N-Terminus
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q96GM1
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Expression Region
1-156aa
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AA Sequence
MAGGRPHLKRSFSIIPCFVFVESVLLGIVILLAYRLEFTDTFPVHTQGFFCYDSTYAKPYPGPEAASRVPPALVYALVTAGPTLTILLGELARAFFPAPPSAVPVIGESTIVSGACCRFSPPVRRLVRFLGVYSFGLFTTTIFANAGQVVTGNPTP
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Molecular Weight
30.7 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
LPPR2 (Liprin-α2) is a member of the liprin family of proteins, which play crucial roles in the regulation of synaptic structure and function. These proteins are primarily involved in organizing synaptic scaffolds and mediating interactions between pre- and postsynaptic components. The study of LPPR2 is particularly important due to its involvement in neurological disorders and its potential role in synaptic plasticity, a fundamental process for learning and memory. Research has shown that alterations in the expression and function of LPPR2 can be linked to neurodevelopmental and neurodegenerative conditions. Understanding the molecular mechanisms by which LPPR2 operates can provide insights into the pathological processes underlying these disorders. Furthermore, the investigation of LPPR2 as a recombinant protein allows researchers to explore its structural features, protein-protein interactions, and functional implications in isolation, facilitating the development of targeted therapies or interventions. As the field of neuroscience continues to unravel the complexities of synaptic regulation, LPPR2 emerges as a promising candidate for advancing our understanding of synaptic health and disease.
