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virus-like particles (VLPs)

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (1) Endogenous Metabolite (1) HIV (1)
By Research Areas:	Cancer (1) Infection (2)
Click Chemistry:	Alkynes (1)

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Click Chemistry

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-122046

Amb123203	Endogenous Metabolite	Infection
Amb123203 is an antiviral compound with the activity of inhibiting viral budding. Amb123203 exerts its effect by blocking the interaction between mVP40 and Nedd4 proteins. Amb123203 has a significant inhibitory effect on the budding of VP40 virus-like particles (VLPs) of Marburg (MARV) and Ebola viruses. Amb123203 can effectively target RNA viruses that rely on the PPxY L domain for efficient budding, showing broad-spectrum antiviral activity. The discovery of Amb123203 provides an important basis for the development of new broad-spectrum antiviral compounds .

HY-185061

HEGA-10	Biochemical Assay Reagents	Others
HEGA-10 is a mild detergent with a high critical micelle concentration (CMC), which can be used to dissolve and extract proteins (HIV-1 spike protein) from the membranes of virus-like particles (VLPs) .

HY-P10845

KRL74	HIV	Infection
KRL74 is a cyclic peptide inhibitor for interaction between the p6 domain of the HIV Gag protein and the UEV domain of the human TSG101 protein(p6/UEV) with an IC₅₀ of 5.44 μM and a K_d of 11.9 μM. KRL74 inhibits the budding process of HIV from host cells with an IC₅₀ of 2 μM in virus-like particle (VLP) budding assay .

Cat. No.	Product Name	Target	Research Area

HY-P10845

KRL74	HIV	Infection
KRL74 is a cyclic peptide inhibitor for interaction between the p6 domain of the HIV Gag protein and the UEV domain of the human TSG101 protein(p6/UEV) with an IC₅₀ of 5.44 μM and a K_d of 11.9 μM. KRL74 inhibits the budding process of HIV from host cells with an IC₅₀ of 2 μM in virus-like particle (VLP) budding assay .

Species:	Virus (3)
Tag:	GFP (1) Tag Free (2)
Source:	HEK293 (3)

Cat. No.	Compare	Product Name	Species	Source	Image

HY-P701236

	Virus-Like Particles (VLPs) isotype control Protein (HEK293) /	Virus	HEK293
	Virus-Like Particles (VLPs) isotype control Protein (HEK293) is an empty virus-like particle, self-assembled from viral envelope or capsid proteins, and serves as a VLP control. Virus-Like Particles (VLPs) isotype control Protein (HEK293) can be used as a control for products such as CD133/PROM1 Protein-VLP, Human (HEK293, His) (HY-P78732), and Claudin-3/CLDN3 Protein-VLP, Human (HEK293, His) (HY-P700472). For more information on controls for other VLP proteins, please refer to the specific protein description. Virus-Like Particles (VLPs) isotype control Protein (HEK293) is a recombinant Virus-Like Particles (VLPs) isotype control Protein expressed by HEK293.

HY-P705433

	Virus-Like Particles (VLPs) isotype control Protein (HEK293, solution)	Virus	HEK293
	Virus-Like Particles (VLPs) isotype control Protein (HEK293, solution) is recommended for the control of CCR7/CD197 Protein-VLP, Human (HEK293)(HY-P704232), Claudin-9/CLDN9 Protein-VLP, Human (HEK293)(HY-P703890), etc. For more control information on other VLP proteins, please refer to the description of the specific protein.

HY-P705435

	Virus-Like Particles (VLPs) isotype control Protein (HEK293, GFP, solution)	Virus	HEK293
	Fluorescent VLP with a GFP tag, self-assembles from viral envelope/capsid proteins, serving as a control for VLPs displaying membrane proteins. Formed in HEK293 cultures, these VLPs concentrate membrane proteins on the cell surface, producing high-concentration proteins ideal for immunization and antibody screening.

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Cat. No.	Product Name		Classification

HY-175421

ArMan		Alkynes
ArMan is an aryl mannoside ligand that can be chemically functionalized onto the surface of virus-like particles (VLPs) through click chemistry. VLPs can be used to target DC-SIGN dendritic cells, promote the selective co-binding of DC-SIGN and TLR7, and lead to a Th1-type immune response. VLP-ArMan-OvaI/II can significantly inhibit tumor growth in the mouse melanoma model .

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BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

MedchemExpress Validation 03

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred

MedchemExpress Validation 04

MedchemExpress Validation

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