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Brand: ProteoGenix

SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant

Note:
For research use only. Not suitable for human use.

$298.00

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Spike protein fragment
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SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant

Product name SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant
Origin species SARS-COV2
Expression system Eukaryotic expression
Sequence   YP_009724390.1
Molecular weight 27kDa
Buffer PBS, pH7.5
Delivery condition Dry Ice
Storage condition 4°C for short term; -20°c or -80°C for long term
Brand ProteoGenix
Host species Mammalian cells
Fragment Type Spike protein fragment
Aliases /Synonyms B.1.1.529, Omicron variant, lineage B.1.1.529, South Africa variant, Botswana variant
Reference PX-COV-P074
Note For research use only. Not suitable for in vitro diagnostic and human use.
Molecular Constructor
Spike protein fragment
Product name SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant
Origin species SARS-COV2
Expression system Eukaryotic expression
Sequence   YP_009724390.1
Molecular weight 27kDa
Buffer PBS, pH7.5
Delivery condition Dry Ice
Storage condition 4°C for short term; -20°c or -80°C for long term
Brand ProteoGenix
Host species Mammalian cells
Fragment Type Spike protein fragment
Aliases /Synonyms B.1.1.529, Omicron variant, lineage B.1.1.529, South Africa variant, Botswana variant
Reference PX-COV-P074
Note For research use only. Not suitable for in vitro diagnostic and human use.
Molecular Constructor
Spike protein fragment

General information on SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant

Lineage B.1.1.529 was reported to WHO in late November 2021 in South Africa. This variant of SARS-CoV-2 accumulates an unprecedented high number of mutations on the spike protein, and especially receptor binding domain (RBD), compared to former variants involved in the Covid-19 pandemic.
The reported mutations are the following : A67V, Δ69-70, T95I, G142D, Δ143-145, Δ211-212, ins214EPE, G339D, S371L, S373P, S375F, K417N, N440K, G446S, S477N, T478K, E484A, Q493K, G496S, Q498R, N501Y, Y505H, T547K, D614G, H655Y, N679K, P681H, N764K, D796Y, N856K, Q954H, N969K, L981F.
The consequences of these new mutations are not yet clear. Some of them had been detected in other variants. K417N and N501Y are typical mutations of the Beta variant from South Africa. S477N had been reported in a variant found in the USA, detected in December 2020, lineage B.1.526.2. Many other mutations are new to the scientific community and need to be studied. According to preliminary results, this new variant might be related to an increased reinfection rate. There are also evidences for a higher growth of the virus.
The PCR tests that have been deployed for other variants still detect it. The efficiency of market vaccines on the omicron variant is currently studied.
After spreading in all South African regions, the variant has been reported in other African countries such as Botswana and then in Europe.
More studies are necessary to determine the precise properties of this variant, especially the impacts of its unreported mutations on transmissibility and the severity its cases of Severe Acute Respiratory Syndrome.

SDS-PAGE for SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant

SDS-PAGE for SARS-CoV-2 RBD of Spike protein– lineage B.1.1.529 – Omicron Variant

SARS-CoV-2 RBD of Spike protein€“ lineage B.1.1.529- Omicron Variant, on SDS-PAGE under reducing. The gel was stained overnight with Coomassie Blue. The purity of the antibody is greater than 95%.

  • Hubert Bernauer, Anja Schlör, Josef Maier, Norbert Bannert, Katja Hanack, Daniel Ivanusic, tANCHOR fast and cost-effective cell-based immunization approach with focus on the receptor-binding domain of SARS-CoV-2, Biology Methods and Protocols, Volume 8, Issue 1, 2023, bpad030, https://doi.org/10.1093/biomethods/bpad030
  • Winklmeier S, Rübsamen H, Özdemir C, Wratil PR, Lupoli G, Stern M, Schneider C, Eisenhut K, Ho S, Wong HK, Taskin D, Petry M, Weigand M, Eichhorn P, Foesel BU, Mader S, Keppler OT, Kümpfel T and Meinl E (2024) Intramuscular vaccination against SARS-CoV-2 transiently induces neutralizing IgG rather than IgA in the saliva. Front. Immunol. 15:1330864. doi: https://doi.org/10.3389/fimmu.2024.1330864
  • Jefferies WA, Choi KB, Ribeca P, et al. A binary self-amplifying expression platform enabling lipid nanoparticle-free vaccines and nanomedicines. Nature Communications. 2025 Dec;16(1):11561. DOI: 10.1038/s41467-025-66252-3. PMID: 41430043; PMCID: PMC12748705.https://doi.org/10.1038/s41467-025-66252-3

  • Emmanuel — August 4, 2022

    Worked for our uses. Originally used a free sample but will be ordering more!

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