c6 36 cell line Search Results


c6 glial cells  (Korean Cell Line Bank)
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Korean Cell Line Bank c6 glial cells
C6 Glial Cells, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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c6/36 insect  (National Centre for Cell Science)
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National Centre for Cell Science c6/36 insect
C6/36 Insect, supplied by National Centre for Cell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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c6 cell line  (Pasteur Institute)
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Pasteur Institute c6 cell line
C6 Cell Line, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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c6/36 jcrb strain  (JCRB Cell Bank)
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JCRB Cell Bank c6/36 jcrb strain
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
C6/36 Jcrb Strain, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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aedes albopictus cell line c6/36  (National Centre for Cell Science)
90
National Centre for Cell Science aedes albopictus cell line c6/36
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
Aedes Albopictus Cell Line C6/36, supplied by National Centre for Cell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mosquito cell line (aedes albopictus; clone c6/36)  (European Collection of Authenticated Cell Cultures)
90
European Collection of Authenticated Cell Cultures mosquito cell line (aedes albopictus; clone c6/36)
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
Mosquito Cell Line (Aedes Albopictus; Clone C6/36), supplied by European Collection of Authenticated Cell Cultures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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c6 glioma (rat glioblastoma) cell line  (National Centre for Cell Science)
90
National Centre for Cell Science c6 glioma (rat glioblastoma) cell line
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
C6 Glioma (Rat Glioblastoma) Cell Line, supplied by National Centre for Cell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rat c6 glioma cells  (Korean Cell Line Bank)
90
Korean Cell Line Bank rat c6 glioma cells
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
Rat C6 Glioma Cells, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rat c6 glioma cells - by Bioz Stars, 2026-03
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c6 rat glioblastoma cells  (Korean Cell Line Bank)
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Korean Cell Line Bank c6 rat glioblastoma cells
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
C6 Rat Glioblastoma Cells, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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c6 cells  (Korean Cell Line Bank)
90
Korean Cell Line Bank c6 cells
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
C6 Cells, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/c6 cells/product/Korean Cell Line Bank
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c6 cells - by Bioz Stars, 2026-03
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rat c6 glioma cell line  (Pasteur Institute)
90
Pasteur Institute rat c6 glioma cell line
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
Rat C6 Glioma Cell Line, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rat c6 glioma cell line - by Bioz Stars, 2026-03
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c6 glioma cells  (Korean Cell Line Bank)
90
Korean Cell Line Bank c6 glioma cells
Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 <t>JCRB</t> strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.
C6 Glioma Cells, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 JCRB strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.

Journal: Heliyon

Article Title: Persistent viruses in mosquito cultured cell line suppress multiplication of flaviviruses

doi: 10.1016/j.heliyon.2018.e00736

Figure Lengend Snippet: Identification of viruses infected in mosquito cultured cell line C6/36. A : Schematics of Shinobi tetravirus (SHTV) and Menghai rhabdovirus (MERV) genomic sequences. Encoded putative genes and their expected sizes are presented (RdRp: RNA-dependent RNA polymerase, VPg: Viral protein genome-linked, CP: capsid protein, N: nucleoprotein, P: phosphoprotein, M: matrix protein, G: glycoprotein, and L: RNA-dependent RNA polymerase). B : Phylogenetic analysis of SHTV and other viruses containing Permutotetraviridae . The amino acid sequences of putative RdRp were aligned and then analyzed using a maximum-likelihood method. Bootstrap replications are shown on the branches. C : Phylogenetic analysis of MERV and other rhabdoviruses. The amino acid sequences of L proteins were analyzed as described. D : Detection of SHTV or MERV in C6/36 JCRB strain and ECACC strain. The viral genome was determined by RT-PCR with the template RNA extracted from cell culture supernatant or cultured cells. PCR amplification from genomic DNA extracted from cultured cells were also determined. J: C6/36 JCRB strain, E: C6/36 ECACC strain. The original image is shown in Supplementary Material 1.

Article Snippet: The growth kinetics of flaviviruses in C6/36 JCRB strain was significantly lower than that in C6/36 ECACC strain ( A).

Techniques: Infection, Cell Culture, Genomic Sequencing, Reverse Transcription Polymerase Chain Reaction, Amplification

C6/36 cells of JCRB and ECACC strains showed different susceptibility to flavivirus infection. Growth kinetics of arboviruses in C6/36 cell lines. A : C6/36 cells of either JCRB or ECACC strain were infected with Zika virus (ZIKV), Japanese encephalitis virus (JEV), or Dengue virus (DENV) at a multiplicity of infection (MOI) of 0.01, and the titers in the supernatants were determined by plaque assay. B : C6/36 cells of either JCRB or ECACC strain were infected with Getah virus (GETV) or Sindbis virus (SINV) with MOI = 0.001. Red lines show the titer in C6/36 JCRB strain and black lines show that in C6/36 ECACC strain. The experiment was triplicated, and the standard deviations are also indicated. Asterisks showed the results of t -test for the data group at each time points (* p < 0.05, ** p < 0.01).

Journal: Heliyon

Article Title: Persistent viruses in mosquito cultured cell line suppress multiplication of flaviviruses

doi: 10.1016/j.heliyon.2018.e00736

Figure Lengend Snippet: C6/36 cells of JCRB and ECACC strains showed different susceptibility to flavivirus infection. Growth kinetics of arboviruses in C6/36 cell lines. A : C6/36 cells of either JCRB or ECACC strain were infected with Zika virus (ZIKV), Japanese encephalitis virus (JEV), or Dengue virus (DENV) at a multiplicity of infection (MOI) of 0.01, and the titers in the supernatants were determined by plaque assay. B : C6/36 cells of either JCRB or ECACC strain were infected with Getah virus (GETV) or Sindbis virus (SINV) with MOI = 0.001. Red lines show the titer in C6/36 JCRB strain and black lines show that in C6/36 ECACC strain. The experiment was triplicated, and the standard deviations are also indicated. Asterisks showed the results of t -test for the data group at each time points (* p < 0.05, ** p < 0.01).

Article Snippet: The growth kinetics of flaviviruses in C6/36 JCRB strain was significantly lower than that in C6/36 ECACC strain ( A).

Techniques: Infection, Virus, Plaque Assay