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SARS-CoV-2 Spike RBD (L452R,T478K) Protein (His Tag)

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  • ¥4500
  • 义翘神州
  • 40592-V08H90
  • 北京
  • 2025年08月12日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      99

    • 英文名

      SARS-CoV-2 Spike RBD (L452R,T478K) Protein (His Tag)

    • 保质期

      12个月

    • 供应商

      北京义翘神州科技股份有限公司

    • 保存条件

      -20℃ to -80℃

    • 规格

      100 µg

    SARS-CoV-2 Spike RBD (L452R,T478K) Protein (His Tag): 产品信息
    纯度> 95 % as determined by SDS-PAGE.
    内毒素< 1.0 EU per μg protein as determined by the LAL method.
    生物活性Testing in progress
    蛋白构建A DNA sequence encoding the SARS-CoV-2 Spike RBD (YP_009724390.1, with mutations L452R,T478K) (Arg319-Phe541) was expressed with a polyhistidine tag at the C-terminus. The mutations were identified in the SARS-CoV-2 variant (known as variant B.1.617.2) which emerged in the India.
    表达宿主HEK293 Cells
    种属SARS-CoV-2
    预测 N 端Arg 319
    分子量The recombinant SARS-CoV-2 Spike RBD consists of 234 amino acids and predicts a molecular mass of 26.6 kDa. As a result of glycosylation, it migrates as an approximately 36.9 kDa band in SDS-PAGE under reducing conditions.
    缓冲液Lyophilized from sterile PBS, pH 7.4.
    Please contact us for any concerns or special requirements.
    Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
    Please refer to the specific buffer information in the hard copy of CoA.
    运输方式In general, recombinant proteins are provided as lyophilized powder which are shipped at ambient temperature.
    Bulk packages of recombinant proteins are provided as frozen liquid. They are shipped out with blue ice unless customers require otherwise.
    稳定性 & 储存条件Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃
    Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
    复溶A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.
     

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    图标文献和实验
    该产品被引用文献
    1, Li C, et al. Broad neutralization of SARS-CoV-2 variants by an inhalable bispecific single-domain antibody.Cell, PubMed ID: 35344711
    2, Emmenegger M, et al. Both COVID-19 infection and vaccination induce high-affinity cross-clade responses to SARS-CoV-2 variants.iScience, PubMed ID: 35875683
    3, Zhang J, et al. Mechanosensing view of SARS-CoV-2 infection by a DNA nano-assembly.Cell Reports Physical Science, PubMed ID: 36157982
    4, Kim JW, et al. Development and Characterization of Phage-Display-Derived Novel Human Monoclonal Antibodies against the Receptor Binding Domain of SARS-CoV-2.Biomedicines, PubMed ID: 36552031
    5, Wang Y, et al. Biparatopic antibody BA7208/7125 effectively neutralizes SARS-CoV-2 variants including Omicron BA.1-BA.5.Cell discovery, PubMed ID: 36609558
    6, Emmenegger M, et al. Protocol to determine antibody affinity and concentration in complex solutions using microfluidic antibody affinity profiling.STAR protocols, PubMed ID: 36853663
    7, Wang M, et al. Oxalic acid blocked the binding of spike protein from SARS-CoV-2 Delta (B.1.617.2) and Omicron (B.1.1.529) variants to human angiotensin-converting enzymes 2.PloS one, PubMed ID: 37200310
    8, Yu X, et al. Discovery of Peptidic Ligands against the SARS-CoV-2 Spike Protein and Their Use in the Development of a Highly Sensitive Personal Use Colorimetric COVID-19 Biosensor.ACS sensors, PubMed ID: 37253267
    9, Zhang RG, et al. SARS-CoV-2 spike protein receptor binding domain promotes IL-6 and IL-8 release via ATP/P2Y2 and ERK1/2 signaling pathways in human bronchial epithelia.Molecular immunology, PubMed ID: 38359646
    10, Chen Y, et al. Structure-Based Optimization of One Neutralizing Antibody against SARS-CoV-2 Variants Bearing the L452R Mutation.Viruses, PubMed ID: 38675908
    11, Park S, et al. An ancestral SARS-CoV-2 vaccine induces anti-Omicron variants antibodies by hypermutation.Nature communications, PubMed ID: 38643233
    相关实验
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      CUT&Tag(Cleavage Under Targets and Tagmentation)是蛋白-DNA 互作的一大革新技术,它不需要使用甲醛交联以及免疫共沉淀,而是通过针对靶蛋白(如转录因子、染色质重塑蛋白)的抗体和 Protein A/G 的介导,使得与 Protein A/G 融合的 Tn5 酶(Tagmentase)在切割 DNA 片段的同时在序列两端加上测序接头,经 PCR 扩增后即可形成用于高通量测序的文库(见图 1 )。CUT &Tag 技术具有细胞投入量低、信噪

    • Chromatin Interaction Analysis Using Paired‐End Tag Sequencing

      , S., Ho, C.H., Irzyk, G.P., Jando, S.C., Alenquer, M.L., Jarvie, T.P., Jirage, K.B., Kim, J.B., Knight, J.R., Lanza, J.R., Leamon, J.H., Lefkowitz, S.M., Lei, M., Li, J., Lohman, K.L., Lu, H., Makhijani, V.B., McDade, K.E., McKenna, M.P., Myers, E.W

    • 新冠病毒及变异株疫苗新突破:环状 RNA 疫苗

      日前,北京大学生命科学学院魏文胜课题组在 Cell 杂志上在线发表题为“Circular RNA Vaccines against SARS-CoV-2 and Emerging Variants”的研究论文。 魏文胜团队首先建立了体外高效制备高纯度环状 RNA 的技术平台,针对新型冠状病毒及其变异株,设计了编码新冠病毒刺突蛋白(Spike)受体结构域(RBD)的环状 RNA 疫苗。 该项研究中制备的针对新冠病毒德尔塔变异株的环状 RNA 疫苗(circRNARBD

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    ¥4500