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plCSA-BP

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Catalog No. TP3682Cas No. 2294870-89-4

plCSA-BP is a placental CSA-binding peptide that specifically binds to trophoblastic cells without interacting with other cell types in the placenta or with CSA-expressing cells in other tissues. It can direct nanoparticles to deliver payloads, such as Indocyanine green (ICG) and Methotrexate (MTX), for targeted placental drug delivery, highlighting its potential in placenta-specific drug delivery research.

plCSA-BP

plCSA-BP

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Catalog No. TP3682Cas No. 2294870-89-4
plCSA-BP is a placental CSA-binding peptide that specifically binds to trophoblastic cells without interacting with other cell types in the placenta or with CSA-expressing cells in other tissues. It can direct nanoparticles to deliver payloads, such as Indocyanine green (ICG) and Methotrexate (MTX), for targeted placental drug delivery, highlighting its potential in placenta-specific drug delivery research.
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
Description
plCSA-BP is a placental CSA-binding peptide that specifically binds to trophoblastic cells without interacting with other cell types in the placenta or with CSA-expressing cells in other tissues. It can direct nanoparticles to deliver payloads, such as Indocyanine green (ICG) and Methotrexate (MTX), for targeted placental drug delivery, highlighting its potential in placenta-specific drug delivery research.
In vivo
plCSA-BP (50 ng/mL) is co-localized with trophoblast cells in mouse placenta at E6.5, E8.5, E10.5, and E12.5, but it does not bind to the embryo, junctional zone, or decidua; similar effects are observed in human placenta. It specifically binds to placental CSA expressed in murine labyrinth and human syncytiotrophoblasts. When plCSA-BP (5 mg/kg, intravenously injected at E12.5 or E15.5) is conjugated to nanoparticles, it specifically delivers ICG to trophoblast cells in pregnant mice at stages E12.5 or E15.5. Additionally, plCSA-BP (5 mg/kg, intravenously injected every other day from E6.5 to E14.5) linked to nanoparticles efficiently targets MTX to placental cells, severely impairing placental and fetal development by targeting placental trophoblast cells.
Chemical Properties
Molecular Weight3186.61
FormulaC142H221N35O44S2
Cas No.2294870-89-4
Smiles[C@@H](CC1=CN=CN1)(NC([C@H](CC2=CC=CC=C2)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC(CNC([C@@H](NC([C@@H](NC([C@H](CC3=CC=CC=C3)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC4=CC=CC=C4)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CCC(O)=O)N)=O)CC(O)=O)=O)[C@@H](C)C)=O)CCCCN)=O)CC(O)=O)=O)[C@H](CC)C)=O)CC(N)=O)=O)=O)CC(O)=O)=O)[C@@H](C)O)=O)CCCCN)=O)CCC(O)=O)=O)CCCCN)=O)=O)CC(C)C)=O)C)=O)=O)CS)=O)CC(C)C)=O)[C@H](CC)C)=O)C(C)C)=O)CO)=O)=O)C(N[C@H](C(NCC(N[C@H](C(N[C@H](C(O)=O)CS)=O)CCCCN)=O)=O)CCC(O)=O)=O
SequenceGlu-Asp-Val-Lys-Asp-Ile-Asn-Phe-Asp-Thr-Lys-Glu-Lys-Phe-Leu-Ala-Gly-Cys-Leu-Ile-Val-Ser-Phe-His-Glu-Gly-Lys-Cys
Sequence ShortEDVKDINFDTKEKFLAGCLIVSFHEGKC
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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