Analytical Data
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Gene name
PLPPR2
- Application
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Alternative Names
PLPPR2；LPPR2；PRG4；Phospholipid phosphatase-related Protein type 2
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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
18.1 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
PLPPR2 (Phospholipid Phosphatase Related 2) is a member of the phospholipid phosphatase family, which plays a crucial role in various cellular processes, including lipid metabolism, cell signaling, and membrane dynamics. This protein is primarily expressed in the central nervous system and has been implicated in neurodevelopment and neural repair mechanisms. Recent studies suggest that PLPPR2 may also have a significant role in the pathology of neurodegenerative diseases, such as Alzheimer's and multiple sclerosis, due to its involvement in myelin sheath formation and maintenance. The investigation of recombinant PLPPR2 protein is vital for understanding its functional roles in cellular pathways and its potential as a therapeutic target. By generating and purifying the recombinant form of PLPPR2, researchers aim to explore its enzymatic activity, binding interactions, and its effects on cell proliferation and differentiation. Furthermore, characterizing the structural properties of PLPPR2 can provide insights into how mutations or dysfunctions in this protein contribute to neurological disorders. Overall, the study of PLPPR2 through recombinant protein technology holds promising potential for advancing our understanding of neurobiology and developing novel interventions for related diseases.
