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Current position:Product Center > Pseudovirus > SARS-CoV-2 pseudovirus > H_ACE2 HEK-293T Cell Line
H_ACE2 HEK-293T Cell Line
Product Info

Cat. No:GM-C12968

Product:H_ACE2 HEK-293T Cell Line


产品配图.jpg


Materials Required

Cell Growth Medium:DMEM+10% FBS+1% P.S+0.75 μg/mL Puromycin

Cell Freezing Medium: 90% FBS+10% DMSO


Description

Angiotensin-converting enzyme (ACE) 2 is a homolog of carboxypeptidase ACE, which generates angiotensin II, the main active peptide of the renin-angiotensin system (RAS). ACE2 is a powerful negative regulator of RAS, balancing the various functions of ACE. By targeting angiotensin II, ACE2 demonstrates protective effects in the cardiovascular system and many other organs. The S protein is a key protein that allows coronaviruses to bind to the ACE2 receptor on the surface of host cells, thereby mediating viral entry into host cells.


The S protein is the most important surface membrane protein of coronaviruses, consisting of two subunits, S1 and S2. The S1 subunit contains the receptor-binding domain (RBD), which is responsible for recognizing the receptors on cells. The S2 subunit contains essential components required for membrane fusion. Studies have shown that the S protein mediates receptor binding and membrane fusion, playing a crucial role in the viral infection of host cells. Additionally, the S protein contains major antigens that stimulate neutralizing antibodies and important targets for cytotoxic lymphocytes, making it a key target for vaccine design, therapeutic antibodies, and diagnostic methods.


Data



Citations

Wang J, Zhang Y, Hu S, Bai H, Xue Z, Liu Y, Ma W. Antiviral drugs suppress infection of 2019-nCoV spike pseudotyped virus by interacting with ACE2 protein. J Biochem Mol Toxicol. 2022 Feb;36(2):e22948. Epub 2021 Nov 10. PMID: 34755435; PMCID: PMC8646714.

Li X, Zhu W, Fan M, Zhang J, Peng Y, Huang F, Wang N, He L, Zhang L, Holmdahl R, Meng L, Lu S. Dependence of SARS-CoV-2 infection on cholesterol-rich lipid raft and endosomal acidification. Comput Struct Biotechnol J. 2021;19:1933-1943. Epub 2021 Apr 8. PMID: 33850607; PMCID: PMC8028701.

Zhang Y, Hu S, Wang J, Xue Z, Wang C, Wang N. Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2. Virology. 2021 Feb;554:83-88.  Epub 2020 Dec 16. PMID: 33387788; PMCID: PMC7744032.

Current position:Product Center > -- > H_ACE2 HEK-293T Cell Line
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H_ACE2 HEK-293T Cell Line
Product Info

Cat. No:GM-C12968

Product:H_ACE2 HEK-293T Cell Line


产品配图.jpg


Materials Required

Cell Growth Medium:DMEM+10% FBS+1% P.S+0.75 μg/mL Puromycin

Cell Freezing Medium: 90% FBS+10% DMSO


Description

Angiotensin-converting enzyme (ACE) 2 is a homolog of carboxypeptidase ACE, which generates angiotensin II, the main active peptide of the renin-angiotensin system (RAS). ACE2 is a powerful negative regulator of RAS, balancing the various functions of ACE. By targeting angiotensin II, ACE2 demonstrates protective effects in the cardiovascular system and many other organs. The S protein is a key protein that allows coronaviruses to bind to the ACE2 receptor on the surface of host cells, thereby mediating viral entry into host cells.


The S protein is the most important surface membrane protein of coronaviruses, consisting of two subunits, S1 and S2. The S1 subunit contains the receptor-binding domain (RBD), which is responsible for recognizing the receptors on cells. The S2 subunit contains essential components required for membrane fusion. Studies have shown that the S protein mediates receptor binding and membrane fusion, playing a crucial role in the viral infection of host cells. Additionally, the S protein contains major antigens that stimulate neutralizing antibodies and important targets for cytotoxic lymphocytes, making it a key target for vaccine design, therapeutic antibodies, and diagnostic methods.


Data



Citations

Wang J, Zhang Y, Hu S, Bai H, Xue Z, Liu Y, Ma W. Antiviral drugs suppress infection of 2019-nCoV spike pseudotyped virus by interacting with ACE2 protein. J Biochem Mol Toxicol. 2022 Feb;36(2):e22948. Epub 2021 Nov 10. PMID: 34755435; PMCID: PMC8646714.

Li X, Zhu W, Fan M, Zhang J, Peng Y, Huang F, Wang N, He L, Zhang L, Holmdahl R, Meng L, Lu S. Dependence of SARS-CoV-2 infection on cholesterol-rich lipid raft and endosomal acidification. Comput Struct Biotechnol J. 2021;19:1933-1943. Epub 2021 Apr 8. PMID: 33850607; PMCID: PMC8028701.

Zhang Y, Hu S, Wang J, Xue Z, Wang C, Wang N. Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2. Virology. 2021 Feb;554:83-88.  Epub 2020 Dec 16. PMID: 33387788; PMCID: PMC7744032.

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