SARS-CoV-2 (2019-nCoV) Spike S2 兔单抗
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SARS-CoV-2 (2019-nCoV) Spike S

2 兔单抗
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  • ¥800 - 2500
  • Sino Biological已认证
  • 北京
  • 40590-T62
  • 2025年09月19日
  • WB,ELISA
  • Rabbit
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    • 详细信息
    • 用户评价
    • 文献和实验
    • 技术资料
    • 免疫原

      Recombinant SARS-CoV-2 / 2019-nCoV Spike/S2 Protein (Catalog#40590-V08B)

    • 亚型

      Rabbit IgG

    • 形态

      液体

    • 保存条件

      在-20℃ to -80℃

    • 克隆性

      PAb

    • 适应物种

    • 保质期

      12个月

    • 抗原来源

      40590-V08B

    • 目录编号

      40590-T62

    • 级别

      免疫学试剂

    • 库存

      99

    • 供应商

      北京义翘神州科技股份有限公司

    • 宿主

      Rabbit

    • 应用范围

      WB,ELISA

    • 浓度

      WB: 1:1000-1:5000;ELISA: 1:5000-1:10000

    • 靶点

      Spike

    • 抗体英文名

      SARS-CoV-2 (2019-nCoV) Spike S2 Antibody, Rabbit PAb, Antigen Affinity Purified

    • 抗体名

      新冠病毒 Spike S2 兔多抗

    • 规格

      20 µL/100 µL

    规格:20 µL产品价格:¥800.0
    规格:100 µL产品价格:¥2500.0

    Coronavirus spike|Coronavirus spike antibody|Coronavirus spike抗体|Anti-2019-nCoV 兔多抗(产品说明)
    抗体种属:2019-nCoV
    抗体靶点:Spike
    抗体应用:WB,ELISA
    抗原货号:40590-V08B
    抗原描述:Recombinant SARS-CoV-2 / 2019-nCoV Spike/S2 Protein (Catalog#40590-V08B)
    抗体宿主:Rabbit
    抗体Ig类型:Rabbit IgG
    抗体纯化方法:Protein A & Antigen Affinity
    抗体制备:Produced in rabbits immunized with recombinant SARS-CoV-2 / 2019-nCoV Spike/S2 Protein (Catalog#40590-V08B; YP_009724390.1; Ser686-Pro1213). The specific IgG was purified by SARS-CoV-2 / 2019-nCoV Spike/S2 affinity chromatography.
    抗体特异性:SARS-CoV-2 (2019-nCoV) Spike S2 (ECD, His tag) (Cat# 40590-V08B)
    抗体保存:This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

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      图标文献和实验
      该产品被引用文献

      1, Takeda Y, et al. Saxifraga spinulosa-Derived Components Rapidly Inactivate Multiple Viruses Including SARS-CoV-2.Viruses, PubMed ID: 32605306
      2, Deinhardt-Emmer S, et al. SARS-CoV-2 causes severe epithelial inflammation and barrier dysfunction.Journal of virology, PubMed ID: 33637603
      3, Dispinseri S, et al. Neutralizing antibody responses to SARS-CoV-2 in symptomatic COVID-19 is persistent and critical for survival.Nature communications, PubMed ID: 33976165
      4, Wang Q, et al. iScience, PubMed ID: 34746689
      5, Kim GN, et al. A vesicular stomatitis virus-based prime-boost vaccination strategy induces potent and protective neutralizing antibodies against SARS-CoV-2.PLoS pathogens, PubMed ID: 34914812
      6, Yu S, et al. SARS-CoV-2 spike engagement of ACE2 primes S2' site cleavage and fusion initiation.Proceedings of the National Academy of Sciences of the United States of America, PubMed ID: 34930824
      7, Lubinski B, et al. Functional evaluation of the P681H mutation on the proteolytic activation of the SARS-CoV-2 variant B.1.1.7 (Alpha) spike.iScience, PubMed ID: 34909610
      8, Shuai H, et al. Attenuated replication and pathogenicity of SARS-CoV-2 B.1.1.529 Omicron.Nature, PubMed ID: 35062016
      9, Du S, et al. The "LLQY" motif on SARS-CoV-2 spike protein affects S incorporation into virus particles.Journal of virology, PubMed ID: 35045269
      10, Frolova EI, et al. Acquisition of Furin Cleavage Site and Further SARS-CoV-2 Evolution Change the Mechanisms of Viral Entry, Infection Spread, and Cell Signaling.Journal of virology, PubMed ID: 35876526
      11, Chan JF, et al. Virological features and pathogenicity of SARS-CoV-2 Omicron BA.2.Cell Reports Medicine, PubMed ID: 36084644
      12, Qu P, et al. Determinants and Mechanisms of the Low Fusogenicity and High Dependence on Endosomal Entry of Omicron Subvariants.mBio, PubMed ID: 36625591
      13, Frolov I, et al. All Domains of SARS-CoV-2 nsp1 Determine Translational Shutoff and Cytotoxicity of the Protein.Journal of virology, PubMed ID: 36847528
      14, Qu P, et al. Enhanced evasion of neutralizing antibody response by Omicron XBB.1.5, CH.1.1, and CA.3.1 variants.Cell reports, PubMed ID: 37104089
      15, Xu D, et al. PLSCR1 is a cell-autonomous defence factor against SARS-CoV-2 infection.Nature, PubMed ID: 37438530
      16, Shuai H, et al. The viral fitness and intrinsic pathogenicity of dominant SARS-CoV-2 Omicron sublineages BA.1, BA.2, and BA.5.EBioMedicine, PubMed ID: 37579626
      17, Liu L, et al. Antibodies targeting a quaternary site on SARS-CoV-2 spike glycoprotein prevent viral receptor engagement by conformational locking.Immunity, PubMed ID: 37776849
      18, Greene KS, et al. Inhibiting Glutamine Metabolism Blocks Coronavirus Replication in Mammalian Cells.bioRxiv : the preprint server for biology, PubMed ID: 37808692
      19, Häring C, et al. The Local Anaesthetic Procaine Prodrugs ProcCluster® and Procaine Hydrochloride Impair SARS-CoV-2 Replication and Egress In Vitro.International journal of molecular sciences, PubMed ID: 37834031
      20, Hu B, et al. Divergent trajectory of replication and intrinsic pathogenicity of SARS-CoV-2 Omicron post-BA.2/5 subvariants in the upper and lower respiratory tract.EBioMedicine, PubMed ID: 38101297
      21, Fan J, et al. Early Emerging SARS-CoV-2 Spike Mutants Are Diversified in Virologic Properties but Elicit Compromised Antibody Responses.Viruses, PubMed ID: 38140642
      22, Qu P, et al. Immune evasion, infectivity, and fusogenicity of SARS-CoV-2 BA.2.86 and FLip variants.Cell, PubMed ID: 38194968
      23, Pérez-Vargas J, et al. Nanomolar anti-SARS-CoV-2 Omicron activity of the host-directed TMPRSS2 inhibitor N-0385 and synergistic action with direct-acting antivirals.Antiviral research, PubMed ID: 38548023
      24, Su W, et al. Furin Egress from the TGN is Regulated by Membrane-Associated RING-CH Finger (MARCHF) Proteins and Ubiquitin-Specific Protease 32 (USP32) via Nondegradable K33-Polyubiquitination.Advanced science (Weinheim, Baden-Wurttemberg, Germany), PubMed ID: 39031635

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      研选
      SARS-CoV-2 (2019-nCoV) Spike S2 兔单抗
      ¥800 - 2500