mt4 cells Search Results


mt4-mmp cell line  (SAS institute)
90
SAS institute mt4-mmp cell line
Mt4 Mmp Cell Line, supplied by SAS institute, 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/product/mt4+cells/pmc02794518-211-2-9?v=SAS+institute
Average 90 stars, based on 1 article reviews
mt4-mmp cell line - by Bioz Stars, 2026-08
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mt4 cells  (JCRB Cell Bank)
90
JCRB Cell Bank mt4 cells
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Mt4 Cells, 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
https://www.bioz.com/product/mt4+cells/pmc03569415-37-6-10?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
mt4 cells - by Bioz Stars, 2026-08
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mt-4 cell line  (CEM Corporation)
90
CEM Corporation mt-4 cell line
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Mt 4 Cell Line, supplied by CEM Corporation, 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/product/mt4+cells/10__3390_slash_app11041877-218-0-6?v=CEM+Corporation
Average 90 stars, based on 1 article reviews
mt-4 cell line - by Bioz Stars, 2026-08
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htlv-1-infected cell lines mt1  (JCRB Cell Bank)
90
JCRB Cell Bank htlv-1-infected cell lines mt1
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Htlv 1 Infected Cell Lines Mt1, 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
https://www.bioz.com/product/mt4+cells/pmc07787980-47-1-11?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
htlv-1-infected cell lines mt1 - by Bioz Stars, 2026-08
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mt-4 cell line  (JCRB Cell Bank)
90
JCRB Cell Bank mt-4 cell line
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Mt 4 Cell Line, 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
https://www.bioz.com/product/mt4+cells/10__1158_slash_2326___6066__cir___15___0148-51-16-7?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
mt-4 cell line - by Bioz Stars, 2026-08
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mt-4 cells  (CEM Corporation)
90
CEM Corporation mt-4 cells
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Mt 4 Cells, supplied by CEM Corporation, 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/product/mt4+cells/pmc03407925-197-2-36?v=CEM+Corporation
Average 90 stars, based on 1 article reviews
mt-4 cells - by Bioz Stars, 2026-08
90/100 stars
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human t-lymphotropic virus type i-infected cell line mt4  (CEM Corporation)
90
CEM Corporation human t-lymphotropic virus type i-infected cell line mt4
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Human T Lymphotropic Virus Type I Infected Cell Line Mt4, supplied by CEM Corporation, 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/product/mt4+cells/10__1074_slash_jbc__m301209200-54-0-14?v=CEM+Corporation
Average 90 stars, based on 1 article reviews
human t-lymphotropic virus type i-infected cell line mt4 - by Bioz Stars, 2026-08
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siv in mt-4 cells  (CEM Corporation)
90
CEM Corporation siv in mt-4 cells
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Siv In Mt 4 Cells, supplied by CEM Corporation, 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/product/mt4+cells/pmc03407925-12-8-3?v=CEM+Corporation
Average 90 stars, based on 1 article reviews
siv in mt-4 cells - by Bioz Stars, 2026-08
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human t lymphocyte cell line mt4  (BioWhittaker Molecular Applications)
90
BioWhittaker Molecular Applications human t lymphocyte cell line mt4
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Human T Lymphocyte Cell Line Mt4, supplied by BioWhittaker Molecular Applications, 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/product/mt4+cells/pm16156786-182-9-20?v=BioWhittaker+Molecular+Applications
Average 90 stars, based on 1 article reviews
human t lymphocyte cell line mt4 - by Bioz Stars, 2026-08
90/100 stars
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mt-4-ltr-egfp cell line  (Tibotec Pharmaceuticals)
90
Tibotec Pharmaceuticals mt-4-ltr-egfp cell line
A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on <t>MT4</t> cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).
Mt 4 Ltr Egfp Cell Line, supplied by Tibotec Pharmaceuticals, 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/product/mt4+cells/pm25103489-35-1-28?v=Tibotec+Pharmaceuticals
Average 90 stars, based on 1 article reviews
mt-4-ltr-egfp cell line - by Bioz Stars, 2026-08
90/100 stars
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cell line ( h. sapiens) mt4  (JCRB Cell Bank)
90
JCRB Cell Bank cell line ( h. sapiens) mt4

Cell Line ( H. Sapiens) Mt4, 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
https://www.bioz.com/product/mt4+cells/pmc07419139-36-7-9?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
cell line ( h. sapiens) mt4 - by Bioz Stars, 2026-08
90/100 stars
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human t-cell lymphotrophic virus-1-transformed t-cell line mt-4  (JCRB Cell Bank)
90
JCRB Cell Bank human t-cell lymphotrophic virus-1-transformed t-cell line mt-4

Human T Cell Lymphotrophic Virus 1 Transformed T Cell Line Mt 4, 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
https://www.bioz.com/product/mt4+cells/10__1074_slash_jbc__m011605200-85-4-11?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
human t-cell lymphotrophic virus-1-transformed t-cell line mt-4 - by Bioz Stars, 2026-08
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Image Search Results


A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on MT4 cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).

Journal: PLoS ONE

Article Title: Novel Gene Therapy Viral Vector Using Non-Oncogenic Lymphotropic Herpesvirus

doi: 10.1371/journal.pone.0056027

Figure Lengend Snippet: A: Growth curves for wtHHV-6 and H6R28LEP in peripheral blood mononuclear cells (PBMCs). PBMCs were infected with wtHHV-6 virus or H6R28LEP at a multiplicity of infection (MOI) of 1. Culture supernatant was collected every 3 d, and 1×10 6 fresh PBMCs were added after each collection. Progeny viruses were titered on MT4 cells by using immunofluroescent assays (wtHHV-6) or by counting EGFP-positive cells (H6R28LEP). Virus titers are indicated in focus-forming units per milliliter (FFU/ml). B: Growth curves for H6R28LEP in PBMCs and cord blood mononuclear cells (CBMCs). PBMCs and CBMCs were infected with H6R28LEP, and progeny viruses were titered every 3 d as described for panel A. C: Replication of viral DNA in PBMCs. PBMCs were infected with H6R28LEP as described, and infected cells were harvested at the indicated times and frozen at −80°C. Infected cells then were incubated with lysis buffer containing 1 mg/ml proteinase K, and the copy numbers of H6R28LEP in cell lysates were quantified by real-time PCR using primers specific for EGFP. Results are given as mean ±1 standard deviation ( n = 3).

Article Snippet: For the titration of recombinant viruses, MT4 cells purchased from JCRB Cell Bank (Saito, Osaka, Japan) were infected and cells positive for enhanced green fluorescent protein (EGFP) were counted 2 d after infection.

Techniques: Infection, Incubation, Lysis, Real-time Polymerase Chain Reaction, Standard Deviation

Journal: eLife

Article Title: MARCH8 inhibits viral infection by two different mechanisms

doi: 10.7554/eLife.57763

Figure Lengend Snippet:

Article Snippet: Cell line ( H. sapiens ) , MT4 , JCRB , 1216 RRID: CVCL_2632 , .

Techniques: Recombinant, Sequencing, Transfection, Enzyme-linked Immunosorbent Assay, Luciferase, Immunoprecipitation, Protease Inhibitor, Western Blot, Immunofluorescence, Software