Mfg Part Number
Ab02059-23.159

Vector Labs Ab02059-23.159 Anti-Spike protein [MR3], Rabbit IgG-Fc Fusion, (200 μg)

Quick Overview
The original antibody was selected after one round of ribosome display using three high diversity libraries (concave, loop and covex) followed by three rounds of phage display and panning against biotinylated RBD as a bait and increasing the stringency of selection with every round. The last round of selection was against 5nM RBD.
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Product Class:Purified
Clone ID:MR3
Synonyms:SARS CoV 2 S glycoprotein; COVID-19 Spike protein; RBD; Receptor Binding Domain; E2 glycoprotein; E2; Human coronavirus 2 spike glycoprotein; Peplomer protein; S glycoprotein; SARS coronavirus 2 S protein; SARS coronavirus 2 Spike Protein; SARS CoV 2 Spike protein; SARS CoV 2; SARS-CoV-2 S protein; SARSCoV2; SARS-COV-2 S protein; SARS-COV-2 Spike glycoprotein; SARSCOV2 Spike protein; Severe acute respiratory syndrome 2 spike glycoprotein; Severe acute respiratory syndrome virus 2 spike glycoprotein; Spike glycoprotein; 2019-nCoV
Amount:200 μg
Application Codes Clone:NTRL; ELISA; FACS; Biolayer interferometry; therapeutic
Shipping Temperature:Wet Ice
Buffer Composition:PBS with 0.02% Proclin 300.
Original Format:VHH
Storage Temperature:Store at 4⁰C for up to 3 months. For longer storage, aliquot and store at -20⁰C.
Chimeric Use Statement:This chimeric rabbit antibody was made using the variable domain sequences of the original VHH format, for improved compatibility with existing reagents, assays and techniques.
Specificity Statement:This antibody binds the receptor binding domain (RBD) of the SARS-CoV-2.
Application Notes:MR3 is a potent antibody that binds the RBD with an affiinty of KD=1.0 nM and neutralizes SARS-CoV-2 pseudovirus with an IC50 of 0.40 µg m/L. Consistent with its highest affinity, MR3 showed the slowest off-rate (2.3 × 10-4 per second). ELISA was used to screen the libraries to identify specific RBD binders. Neutralization activity of the sybody was checked by pre-incubating pseudoviral particles with different concentrations of sybody before infection of VeroE6-hACE2 cells. The rate of infection was then measured by fluorescence-activated cell sorting (FACS). The binding kinetics between sybodies and the RBD was assessed using bio-layer interferometry (Li et al., 2020).
More Information
Brand Vector Labs
UNSPSC 12161500