pPB peptide
Based on 1 Customer Validation
pPB peptide is a cyclic peptide targeting platelet-derived growth factor receptor β (PDGFRβ). Derived from natural platelet-derived growth factor (PDGF), pPB peptide contains arginine and isoleucine as key receptor-binding residues. pPB peptide specifically binds to PDGFRβ, which is highly expressed on the surface of activated hepatic stellate cells (HSC). pPB peptide can be used in studies related to liver fibrosis, liver cirrhosis, and tumor-specific drug delivery.
For research use only. We do not sell to patients.
- CAS No.: 663933-94-6
- Formula: C35H60N12O13S2
- Molecular Weight:921.05
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Storage:
Sealed storage, away from moisture.
Powder -80°C, 2 years , -20°C, 1 year* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Biological Activity
Description
IC50 & Target
[1]|
PDGFRβ |
In Vitro
The pPB peptide is successfully conjugated to pegylated hollow polydopamine nanoparticles, with a molar grafting ratio of 1.50%[1].
The pPB peptide can be conjugated to form DSPE-PEG-pPB[2].
Modification with pPB peptide (6 weeks) does not significantly alter the particle size distribution, charge or morphology of SNALPs, and SNALPs modified with 2% pPB remain stable for at least 6 weeks[2].
The pPB peptide mediates enhanced uptake of SNALPs by hepatic stellate cells (HSCs) through specific binding to the PDGFR-β receptor on HSCs[2].
Modification with the pPB peptide enhances the gene silencing effects on HSP47 and HMGB1 in hepatic stellate cells (HSCs) by improving the uptake efficiency of SNALP[2].
The pPB peptide successfully conjugates with DMPE-PEG-Mal to form the DPP construct[3].
PPB peptide (1 μg/mL; 2 h) mediates PDGFβR-specific, species-nonspecific binding of IFNγ conjugates to mouse NIH3T3 fibroblasts, human LX2 hepatic stellate cells, and primary rat hepatic stellate cells[4].
The PPB peptide (2 h) significantly reduces TGFβ1-induced collagen expression in mouse NIH3T3 fibroblasts and human LX2 hepatic stellate cells when combined with IFNγ, overcoming the limitation of species-specific IFNγ receptors in human cells[4].
Conjugation of the PPB peptide with IFNγ mediates the inhibition of PDGF-induced proliferation of mouse NIH3T3 fibroblasts[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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CAS No. 663933-94-6
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Appearance Solid
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Molecular Weight 921.05
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Formula C35H60N12O13S2
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Sequence
Cys-Ser-Arg-Asn-Leu-Ile-Asp-Cys (disulfide bridge:Cys1-Cys8)
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Sequence Shortening
CSRNLIDC (disulfide bridge:Cys1-Cys8)
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Sealed storage, away from moisture
Powder -80°C 2 years -20°C 1 year * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Protocols
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Fibrosis/Collagen Morphometry
Fibrosis and collagen morphometry is based on the quantitative visualization of fibrillar collagen deposition in tissue sections using histochemical stains such as Sirius Red (Picrosirius Red) or Masson's trichrome, followed by image-based or polarization-enhanced analysis to estimate collagen proportional area as a surrogate of extracellular matrix accumulation during fibrotic remodeling. Sirius Red combined with polarized light microscopy enhances detection of collagen fibers due to birefringence properties, enabling more specific visualization of collagen type I and III fibrils compared to conventional bright-field histology, while whole-section or region-restricted digital morphometry reduces field-selection bias in fibrosis assessment. Alternative quantitative approaches include second harmonic generation (SHG) and two-photon excited fluorescence microscopy, which enable label-free detection of fibrillar collagen and have been validated against histological staining and biochemica
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Collagen: Sirius Red Staining
Sirius Red or picrosirius red staining is a histochemical method for visualizing collagen-rich extracellular matrix in tissue sections, and collagen fibers are detected as red-stained structures under bright-field microscopy with enhanced birefringence under polarized light. Picrosirius red is useful for assessing total collagen organization, distribution, and fibrosis burden, but polarized color should not be interpreted as a definitive collagen type I versus type III readout because color is affected by fiber orientation, thickness, and packing.
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Connective Tissue: Masson's Trichrome/Collagen Trichrome Staining
Masson’s Trichrome (collagen/trichrome staining) is a histological technique that differentially stains tissue compartments using sequential acidic dyes to distinguish collagen from muscle and cytoplasmic components based on dye affinity and tissue permeability differences, enabling visualization of fibrosis and connective tissue architecture in histological sections. The classical formulation typically uses Weigert's iron hematoxylin for nuclear staining, Biebrich scarlet-acid fuchsin for cytoplasm and muscle, and aniline blue (or light green variants) for collagen, producing a characteristic blue/green collagen signal contrasted against red cytoplasm and dark nuclei. The staining principle relies on selective displacement of smaller dye molecules by larger anionic dyes in collagen-rich regions under controlled acidified conditions, which enhances collagen-specific dye retention. This property makes the method widely used for fibrosis assessment in organs such as heart, liver, lung, a
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Liver Histomorphometry
Liver histomorphometry is a quantitative histological approach used to measure structural alterations in hepatic tissue, including parenchymal loss, steatosis, fibrosis, and vascular remodeling, by combining stained tissue section analysis with stereological or computerized image-based measurements. Classical morphometric frameworks quantify volume fractions of liver compartments and fibrotic regions using systematic sampling and image analysis, enabling objective comparison of pathological changes across experimental groups. These approaches are widely applied in liver cirrhosis and fibrosis studies to reduce subjectivity in histological scoring and improve reproducibility of tissue evaluation. Recent methodological advances integrate automated image analysis and radiomics-based extraction of histological features from standard liver stains (e. g. , H&E and fibrotic stains), enabling quantitative correlation between morphometric features and fibrosis stages in non-alcoholic fatty live
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)