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AB169442

Anti-Enterovirus 71 antibody

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(13 Publications)

Mouse Polyclonal POLG antibody. Carrier free. Suitable for WB and reacts with Transfected cell lysate - Enterovirus A71 samples. Cited in 13 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human enterovirus 71 (strain BRCR) Genome polyprotein.

View Alternative Names

Genome polyprotein

1 Images
Western blot - Anti-Enterovirus 71 antibody (AB169442)
  • WB

Unknown

Western blot - Anti-Enterovirus 71 antibody (AB169442)

All lanes:

Western blot - Anti-Enterovirus 71 antibody (ab169442) at 1 µg/mL

Lane 1:

Enterovirus 71 transfected lysate at 15 µL

Lane 2:

Non-transfected lysate at 15 µL

Predicted band size: 33 kDa

false

Key facts

Host species

Mouse

Clonality

Polyclonal

Isotype

IgG

Carrier free

Yes

Reacts with

Enterovirus A71

Applications

WB

applications

Immunogen

Recombinant Full Length Protein corresponding to Human enterovirus 71 (strain BRCR) Genome polyprotein.

Q66478

Specificity

This antibody is specific for the Protein VP1 cleaved chain of Genome polyprotein. The complete proteome is Human enterovirus 71 (Ev 71).

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Enterovirus 71 (EV71) also known as enteroviral VP1 is a significant member of the enterovirus genus. Mechanically EV71 is a small RNA virus with a protein capsid that is important for viral replication and cell infection. The virus is around 30 nm in diameter and the capsid proteins including VP1 play an important role in its structure and function. EV71 is primarily expressed in human tissues that include the gastrointestinal tract and central nervous system. The VP1 protein is essential for receptor recognition and mediates the attachment of the virus to host cells facilitating the entry of the viral RNA into the host cell.
Biological function summary

EV71 infects host cells and hijacks the cellular machinery to replicate itself causing cytopathic effects. The VP1 protein is a critical part of the viral capsid complex and interacts with host cell receptors initiating infection. This process causes the host cell to undergo apoptosis and releases new viral particles perpetuating the infection cycle. EV71 plays a substantial role in disrupting host cellular processes which then leads to notable clinical symptoms.

Pathways

EV71 interacts with host cellular pathways involved in viral replication and immune response. Specifically the virus can affect the signal transduction pathways important for the host's antiviral defenses such as the type I interferon pathway. This interaction allows the virus to evade the immune system temporarily. Additionally EV71 affects the proteasome pathway that includes proteins related to antigen presentation which is essential for an adequate immune response by the host.

EV71 is most notably associated with hand foot and mouth disease and can cause severe neurological complications like encephalitis. The virus can affect young children severely and outbreaks have led to significant health concerns in various regions. EV71 interacts with proteins involved in immune surveillance such as those within the interferon response pathways which play a critical role in the pathogenesis of its related diseases. Understanding this interaction is important for developing therapeutic monoclonal antibodies such as mab979 that can target EV71 infections.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Capsid protein VP1. Forms an icosahedral capsid of pseudo T=3 symmetry with capsid proteins VP2 and VP3 (By similarity). The capsid is 300 Angstroms in diameter, composed of 60 copies of each capsid protein and enclosing the viral positive strand RNA genome (By similarity). Capsid protein VP1 mainly forms the vertices of the capsid (By similarity). Capsid protein VP1, together with VP2, interacts with host cell receptor SCARB2 to provide virion attachment to target host cells. This attachment induces virion internalization predominantly through clathrin-dependent endocytosis (PubMed : 20956521, PubMed : 37417384). After binding to its receptor, the capsid undergoes conformational changes (By similarity). Capsid protein VP1 N-terminus (that contains an amphipathic alpha-helix) and capsid protein VP4 are externalized (By similarity). Together, they shape a pore in the host membrane through which viral genome is translocated to host cell cytoplasm (By similarity).. Capsid protein VP2. Forms an icosahedral capsid of pseudo T=3 symmetry with capsid proteins VP2 and VP3 (By similarity). The capsid is 300 Angstroms in diameter, composed of 60 copies of each capsid protein and enclosing the viral positive strand RNA genome (By similarity). Capsid protein VP2, together with VP1, interacts with host cell receptor SCARB2 to provide virion attachment to target host cells (By similarity).. Capsid protein VP3. Forms an icosahedral capsid of pseudo T=3 symmetry with capsid proteins VP2 and VP3 (By similarity). The capsid is 300 Angstroms in diameter, composed of 60 copies of each capsid protein and enclosing the viral positive strand RNA genome (By similarity).. Capsid protein VP4. Lies on the inner surface of the capsid shell (By similarity). After binding to the host receptor, the capsid undergoes conformational changes (By similarity). Capsid protein VP4 is released, Capsid protein VP1 N-terminus is externalized, and together, they shape a pore in the host membrane through which the viral genome is translocated into the host cell cytoplasm (By similarity).. Capsid protein VP0. Component of immature procapsids, which is cleaved into capsid proteins VP4 and VP2 after maturation (By similarity). Allows the capsid to remain inactive before the maturation step (By similarity).. Protease 2A. Cysteine protease that cleaves viral polyprotein and specific host proteins (By similarity). It is responsible for the autocatalytic cleavage between the P1 and P2 regions, which is the first cleavage occurring in the polyprotein (By similarity). Cleaves also the host translation initiation factor EIF4G1, in order to shut down the capped cellular mRNA translation (By similarity). Inhibits the host nucleus-cytoplasm protein and RNA trafficking by cleaving host members of the nuclear pores (By similarity). Counteracts stress granule formation probably by antagonizing its assembly or promoting its dissassembly (PubMed : 30867299). Cleaves and inhibits host IFIH1/MDA5, thereby inhibiting the type-I IFN production and the establishment of the antiviral state (PubMed : 24390337). Cleaves and inhibits host MAVS, thereby inhibiting the type-I IFN production and the establishment of the antiviral state (PubMed : 24390337, PubMed : 28253362).. Protein 2B. Plays an essential role in the virus replication cycle by acting as a viroporin. Creates a pore in the host reticulum endoplasmic and as a consequence releases Ca2+ in the cytoplasm of infected cell (By similarity). In turn, high levels of cytoplasmic calcium may trigger membrane trafficking and transport of viral ER-associated proteins to viroplasms, sites of viral genome replication (By similarity). Activates also the mitochondrial apoptotic pathway by activating host BAX (PubMed : 27558414).. Protein 2C. Induces and associates with structural rearrangements of intracellular membranes. Displays RNA-binding, nucleotide binding and NTPase activities. May play a role in virion morphogenesis and viral RNA encapsidation by interacting with the capsid protein VP3.. Protein 3AB. Localizes the viral replication complex to the surface of membranous vesicles. Together with protein 3CD binds the Cis-Active RNA Element (CRE) which is involved in RNA synthesis initiation. Acts as a cofactor to stimulate the activity of 3D polymerase, maybe through a nucleid acid chaperone activity.. Protein 3A. Localizes the viral replication complex to the surface of membranous vesicles (By similarity). It inhibits host cell endoplasmic reticulum-to-Golgi apparatus transport and causes the disassembly of the Golgi complex, possibly through GBF1 interaction (By similarity). This would result in depletion of MHC, trail receptors and IFN receptors at the host cell surface (By similarity). Plays an essential role in viral RNA replication by recruiting ACBD3 and PI4KB at the viral replication sites, thereby allowing the formation of the rearranged membranous structures where viral replication takes place (Probable).. Viral protein genome-linked. Acts as a primer for viral RNA replication and remains covalently bound to viral genomic RNA. VPg is uridylylated prior to priming replication into VPg-pUpU (By similarity). The oriI viral genomic sequence may act as a template for this. The VPg-pUpU is then used as primer on the genomic RNA poly(A) by the RNA-dependent RNA polymerase to replicate the viral genome (By similarity). Following genome release from the infecting virion in the cytoplasm, the VPg-RNA linkage is probably removed by host TDP2 (By similarity). During the late stage of the replication cycle, host TDP2 is excluded from sites of viral RNA synthesis and encapsidation, allowing for the generation of progeny virions (By similarity).. Protein 3CD. Involved in the viral replication complex and viral polypeptide maturation. It exhibits protease activity with a specificity and catalytic efficiency that is different from protease 3C. Protein 3CD lacks polymerase activity. Protein 3CD binds to the 5'UTR of the viral genome. Regulates host protein expression by interacting with host PPP1R15A to support viral replication (PubMed : 34985336).. Protease 3C. Major viral protease that mediates proteolytic processing of the polyprotein (By similarity). Cleaves host EIF5B, contributing to host translation shutoff (By similarity). Cleaves also host PABPC1, contributing to host translation shutoff (By similarity). Disassembles host cytoplasmic stress granules by cleaving host G3BP1, although this effect is less prononced than the inhibition induced by protease 2A (PubMed : 30006004, PubMed : 30867299). Cleaves host RIGI and thus contributes to the inhibition of type I interferon production (PubMed : 24390337). Cleaves host IRF7 and thus contributes to the inhibition of type I interferon production (PubMed : 23175366). Cleaves host HNRNPA1 thereby increasing the translation of apoptosis protease activating factor APAF1, leading to apoptosis of the host cell (PubMed : 31498791). Cleaves host NLRP1, triggers host N-glycine-mediated degradation of the autoinhibitory NLRP1 N-terminal fragment (PubMed : 33410748). Cleaves and inactivates host GSDMD, preventing GSDMD-mediated pyroptosis (PubMed : 28679757). Promotes also apoptosis in infected cell through cleaving of host PINX1, a telomere binding protein in order to facilitate viral release (PubMed : 27847364). Impairs host PML-NBs production via PML cleavage and counter its antiviral activities (PubMed : 34930370).. RNA-directed RNA polymerase. Replicates the viral genomic RNA on the surface of intracellular membranes. May form linear arrays of subunits that propagate along a strong head-to-tail interaction called interface-I. Covalently attaches UMP to a tyrosine of VPg, which is used to prime RNA synthesis. The positive stranded RNA genome is first replicated at virus induced membranous vesicles, creating a dsRNA genomic replication form. This dsRNA is then used as template to synthesize positive stranded RNA genomes. ss(+)RNA genomes are either translated, replicated or encapsidated. Facilitates the assembly of NLRP3 inflammasome complex and stimulates the cleavage of host pro-CASP1 and the secretion of IL-1beta (PubMed : 28060938).
See full target information Genome polyprotein

Additional targets

Enterovirus 71

Publications (13)

Recent publications for all applications. Explore the full list and refine your search

Virologica Sinica 39:632-644 PubMed38945214

2024

AIMP2 restricts EV71 replication by recruiting SMURF2 to promote the degradation of 3D polymerase.

Applications

Unspecified application

Species

Unspecified reactive species

Junrui Ren,Lei Yu,Qiuhan Zhang,Pengyu Ren,Yumeng Cai,Xueyun Wang,Ke Lan,Shuwen Wu

The Journal of cell biology 222: PubMed37906052

2023

Inhibition of lysosome-tethered Ragulator-Rag-3D complex restricts the replication of Enterovirus 71 and Coxsackie A16.

Applications

Unspecified application

Species

Unspecified reactive species

Xinhui Wang,Zhilin Hu,Wei Zhang,Shuwei Wu,Yongjin Hao,Xia Xiao,Jingjing Li,Xiaoliang Yu,Chengkui Yang,Jingfeng Wang,Huiying Zhang,Feng Ma,Weifeng Shi,Jianwei Wang,Xiaobo Lei,Xiaohu Zhang,Sudan He

Journal of virology 97:e0078623 PubMed37796126

2023

Ubiquitin E3 ligase SPOP is a host negative regulator of enterovirus 71-encoded 2A protease.

Applications

Unspecified application

Species

Unspecified reactive species

Lichao Zang,Xinyu Yang,Yan Chen,Fan Huang,Yukang Yuan,Xiangjie Chen,Yibo Zuo,Ying Miao,Jin Gu,Hui Guo,Wenxin Xia,Yang Peng,Mengyuan Tang,Ziwei Huang,Yangyang Wang,Jinhong Ma,Jingting Jiang,Wei Zhou,Hui Zheng,Weifeng Shi

Virologica Sinica 38:75-83 PubMed36334706

2022

Ubiquitin-specific protease 24 promotes EV71 infection by restricting K63-linked polyubiquitination of TBK1.

Applications

Unspecified application

Species

Unspecified reactive species

Lichao Zang,Jin Gu,Xinyu Yang,Yukang Yuan,Hui Guo,Wei Zhou,Jinhong Ma,Yan Chen,Yumin Wu,Hui Zheng,Weifeng Shi

Frontiers in microbiology 12:762869 PubMed34992585

2021

Enterovirus A71 2B Inhibits Interferon-Activated JAK/STAT Signaling by Inducing Caspase-3-Dependent Karyopherin-α1 Degradation.

Applications

Unspecified application

Species

Unspecified reactive species

Menghuai Sun,Qian Lin,Chunyang Wang,Jiao Xing,Kunlong Yan,Zhifeng Liu,Yu Jin,Carol J Cardona,Zheng Xing

Virologica Sinica 36:1387-1399 PubMed34196914

2021

ANXA2 Facilitates Enterovirus 71 Infection by Interacting with 3D Polymerase and PI4KB to Assist the Assembly of Replication Organelles.

Applications

Unspecified application

Species

Unspecified reactive species

Qiuhan Zhang,Siliang Li,Ping Lei,Zixian Li,Feifei Chen,Qi Chen,Yulu Wang,Jiami Gong,Qi Tang,Xinjin Liu,Ke Lan,Shuwen Wu

Intervirology 64:147-155 PubMed33951637

2021

The Upregulation of a Novel Long Noncoding RNA AK097647 Promotes Enterovirus 71 Replication and Decreases IFN-λ1 Secretion.

Applications

Unspecified application

Species

Unspecified reactive species

Min Chu,Bingfei Zhou,Huilin Tu,Min Li,Li Huang,Yuan He,Luo Liu,Song Han,Jun Yin,Biwen Peng,Xiaohua He,Wanhong Liu

Annals of transplantation 26:e924461 PubMed33397838

2021

Transplantation of Enterovirus 71 Virion Protein Particle Vaccine Protects Against Enterovirus 71 Infection in a Neonatal Mouse Model.

Applications

Unspecified application

Species

Unspecified reactive species

Li Lei,Qing Li,Shuhong Xu,Mingyang Tian,Xinghui Zheng,Yunxia Bi,Bo Huang

Emerging microbes & infections 9:427-438 PubMed32079505

2020

An infectious clone of enterovirus 71(EV71) that is capable of infecting neonatal immune competent mice without adaptive mutations.

Applications

Unspecified application

Species

Unspecified reactive species

Huiying Zhang,Zhigang Song,Jingyi Zou,Yanling Feng,Jing Zhang,Lehao Ren,Xiaonan Zhang,Yunwen Hu,Zhenghong Yuan,Zhigang Yi

Viruses 12: PubMed31861844

2019

Enterovirus 71 VP1 Protein Regulates Viral Replication in SH-SY5Y Cells via the mTOR Autophagy Signaling Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Zi-Wei Liu,Zhi-Chao Zhuang,Rui Chen,Xiao-Rui Wang,Hai-Lu Zhang,Shu-Han Li,Zhi-Yu Wang,Hong-Ling Wen
View all publications

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