Anti-Envelope protein [5A]
AB03416-23.0-BT
ApplicationsFunctional Assay, ImmunoPrecipitation, ELISA, Neutralisation/Blocking, Other Application
Product group Antibodies
ReactivityVirus
TargetPOLY
Overview
- SupplierAbsolute Antibody
- Product NameAnti-Envelope protein [5A]
- Delivery Days Customer9
- Application Supplier NoteThe specificity of the scFv format of the antibody was confirmed by ELISA analysis. The antibody showed 50% and 100% neutralizing activity in plaque reduction neutralization assay (PRNT) using Vero cells against YFV strains 17D-204-WHO and Asibi at concentrations of approximately 1 microg/ml and 10 microg/ml, respectively. The antibody neutralized wild-type YFV strains of genotypes West Africa I (Nigeria 1987) and II (Asibi) and East/Central Africa (CAR 1986, Ethiopia 1961) with comparable efficiency in a PRNT on PS cells. Competitive ELISA showed that the scFv fragment competed for binding to YFV-17D virions with Ab02826. An immunoprecipitation assay with radiolabeled, purified YFV-17D virions was performed. The scFv fragment was found to precipitate a 55-kDa protein, corresponding to the molecular weight of the envelope glycoprotein (Daffis et al., 2005; PMID: 15919103). The structure of the scFv fragment of the antibody in complex with the E protein was determined. Surface plasmon resonance (SPR) experiments showed that the antibody bound to sE proteins from both YFV-17D and YFV-China with high affinities (KD values are 13.5 nM and 9.7 nM, respectively). The in vitro neutralizing activity for YFV was assessed using a modified fluorescence-activated cell sorting (FACS)-based assay in Vero cells. The antibody displayed extremely high neutralization activity against both YFV strains (IC50, 15 ng/mL and 6 ng/mL for YFV-China and YFV-17D, respectively). Mice treated with the antibody were completely protected against YFV-17D infection. Pre- and post-attachment neutralization assays were carried out in BHK-21 cells. In both cases the antibody efficiently neutralized the virus ((IC50= 19 ng/mL and IC50= 8 ng/mL respectively). Finally, the antibody partially blocked pH-dependent fusion of YFV-17D with liposomes (IC50, 19 ng/mL) (Lu et al., 2019).
- ApplicationsFunctional Assay, ImmunoPrecipitation, ELISA, Neutralisation/Blocking, Other Application
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID5A
- Gene ID1502173
- Target namePOLY
- Target descriptionpolyprotein
- Target synonymsYFVgp1, polyprotein, 2K protein, M protein precursor, RNA-dependent RNA polymerase, anchored core protein C, core protein C, envelope protein, matrix protein M, non-structural protein NS1, non-structural protein NS2a, non-structural protein NS2b, non-structural protein NS3, non-structural protein NS4a, non-structural protein NS4b
- HostRabbit
- IsotypeIgG
- Protein IDP03314
- Protein NameGenome polyprotein
- Scientific DescriptionThis full-length chimeric rabbit antibody was made using the variable domain sequences of the original Human ScFv format for improved compatibility with existing reagents assays and techniques.
- ReactivityVirus
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC41116161

![Various viral lysates (0.1 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with Yellow Fever virus Envelope Protein antibody [HL2409] (GTX638626) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX638626/GTX638626_T-45061_20230825_WB_multiplevirus_23083020_434.webp)
