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  • 92
    ATCC bei atcc
    Bei Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC atcc bei mr4 repository
    Atcc Bei Mr4 Repository, supplied by ATCC, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    BEI Resources bei resource
    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV <t>RNA</t> ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei Resource, supplied by BEI Resources, used in various techniques. Bioz Stars score: 93/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    BEI Resources bei
    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV <t>RNA</t> ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei, supplied by BEI Resources, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    BEI Resources bei deposit
    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV <t>RNA</t> ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei Deposit, supplied by BEI Resources, used in various techniques. Bioz Stars score: 92/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    ATCC vero e6 bei
    Filovirus plaques produced on <t>Vero</t> <t>E6</t> cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on <t>BEI</t> Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.
    Vero E6 Bei, supplied by ATCC, used in various techniques. Bioz Stars score: 85/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    BEI Resources bei resources nrs
    Filovirus plaques produced on <t>Vero</t> <t>E6</t> cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on <t>BEI</t> Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.
    Bei Resources Nrs, supplied by BEI Resources, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    ATCC bei strain repository
    Filovirus plaques produced on <t>Vero</t> <t>E6</t> cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on <t>BEI</t> Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.
    Bei Strain Repository, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    BEI Resources infections bei resources
    Filovirus plaques produced on <t>Vero</t> <t>E6</t> cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on <t>BEI</t> Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.
    Infections Bei Resources, supplied by BEI Resources, used in various techniques. Bioz Stars score: 85/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    BEI Resources bei resources stock
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei Resources Stock, supplied by BEI Resources, used in various techniques. Bioz Stars score: 85/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    BEI Resources bei resources nr 86
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei Resources Nr 86, supplied by BEI Resources, used in various techniques. Bioz Stars score: 88/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    BEI Resources bei resources nr 80
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei Resources Nr 80, supplied by BEI Resources, used in various techniques. Bioz Stars score: 88/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    BEI Resources infectious research bei resources
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Infectious Research Bei Resources, supplied by BEI Resources, used in various techniques. Bioz Stars score: 93/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    BEI Resources bei resources strain repository
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from <t>BEI</t> resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Bei Resources Strain Repository, supplied by BEI Resources, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    ATCC atcc virology
    Filovirus plaques produced on <t>Vero</t> E6 cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on <t>ATCC</t> Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on BEI Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.
    Atcc Virology, supplied by ATCC, used in various techniques. Bioz Stars score: 85/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    ATCC atcc collection
    Filovirus plaques produced on <t>Vero</t> E6 cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on <t>ATCC</t> Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on BEI Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.
    Atcc Collection, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 30 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    ATCC atcc tcrv stocks
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and <t>ATCC</t> TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Atcc Tcrv Stocks, supplied by ATCC, used in various techniques. Bioz Stars score: 85/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC atcc tcrv stock
    Analysis of a <t>TCRV</t> NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and <t>ATCC</t> TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p
    Atcc Tcrv Stock, supplied by ATCC, used in various techniques. Bioz Stars score: 85/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC b mallei atcc 23344
    The 50% lethal dose of B. mallei <t>ATCC</t> 23344 when administered by oropharyngeal aspiration. Five doses of 10-fold serial dilutions were prepared to administer 3.8×10 5 cfu, 3.6×10 4 cfu, 3.36×10 3 cfu, 366 cfu and 36 cfu of B. mallei ATCC 23344 to BALB/c mice by OA as described as described in the materials and methods and Fig. 1 . Mice were observed for 14 days. The actual inhaled doses are shown in the graph and were utilized to calculate LD 50 (1.7×10 3 cfu).
    B Mallei Atcc 23344, supplied by ATCC, used in various techniques. Bioz Stars score: 91/100, based on 790 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Journal: The Journal of Biological Chemistry

    Article Title: Identification of Critical Amino Acids within the Nucleoprotein of Tacaribe Virus Important for Anti-interferon Activity *

    doi: 10.1074/jbc.M112.444760

    Figure Lengend Snippet: Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Article Snippet: Viral RNA from sucrose cushion-purified TCRV passaged once in Vero cells from original BEI resources or ATCC stocks was extracted using QIAamp UltraSens Virus kit (Qiagen). cDNA synthesis using random primers was performed using a MMLV reverse transcriptase first-strand cDNA synthesis kit (Epicenter).

    Techniques: Activity Assay, Sequencing, Derivative Assay, Expressing, Infection, Transfection, Molecular Weight, Purification, Plasmid Preparation, Activation Assay, Positive Control

    Filovirus plaques produced on Vero E6 cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on BEI Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.

    Journal: Viruses

    Article Title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies

    doi: 10.3390/v4123511

    Figure Lengend Snippet: Filovirus plaques produced on Vero E6 cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on BEI Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.

    Article Snippet: In general, there did not appear to be a noticeable trend indicating any decrease in viral titer measured in the BEI Vero E6 cells, but there may be a slight trend in decrease of titer over time in the ATCC Vero E6 cells.

    Techniques: Produced

    Vero E6 cells are suitable for quantitation of EBOV plaques. ( A ) Vero and Vero E6 cells produce EBOV plaques. ( B ) EBOV titers are similar in ATCC Vero E6 cells plated 24, 48 or 72 hours prior to plaque assay. This experiment was performed twice, and one representative graph is shown. Each bar represents an average of 5 replicates. The * indicates p = 0.006 between 24 and 72 hour samples for passage 29.

    Journal: Viruses

    Article Title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies

    doi: 10.3390/v4123511

    Figure Lengend Snippet: Vero E6 cells are suitable for quantitation of EBOV plaques. ( A ) Vero and Vero E6 cells produce EBOV plaques. ( B ) EBOV titers are similar in ATCC Vero E6 cells plated 24, 48 or 72 hours prior to plaque assay. This experiment was performed twice, and one representative graph is shown. Each bar represents an average of 5 replicates. The * indicates p = 0.006 between 24 and 72 hour samples for passage 29.

    Article Snippet: In general, there did not appear to be a noticeable trend indicating any decrease in viral titer measured in the BEI Vero E6 cells, but there may be a slight trend in decrease of titer over time in the ATCC Vero E6 cells.

    Techniques: Quantitation Assay, Plaque Assay

    ( A ) EBOV titers in ATCC or BEI Vero E6 cells of various passage ages. This experiment was performed by three independent investigators, four replicates per cell type. The combined data are presented, where each bar represents 12 replicates. * indicates a significant difference in value between BEI passage 40 and passage 27 ( p = 0.0003), ** a difference between ATCC passage 54 and 28 ( p = 0.007), and *** a difference between BEI passage 40 and ATCC passage 28 ( p = 0.000002). For these experiments, p value cutoff was ≤0.008). ( B ) Analysis of EBOV titer changes in cells of various passages. The arrows point out data from passages plotted in (A).

    Journal: Viruses

    Article Title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies

    doi: 10.3390/v4123511

    Figure Lengend Snippet: ( A ) EBOV titers in ATCC or BEI Vero E6 cells of various passage ages. This experiment was performed by three independent investigators, four replicates per cell type. The combined data are presented, where each bar represents 12 replicates. * indicates a significant difference in value between BEI passage 40 and passage 27 ( p = 0.0003), ** a difference between ATCC passage 54 and 28 ( p = 0.007), and *** a difference between BEI passage 40 and ATCC passage 28 ( p = 0.000002). For these experiments, p value cutoff was ≤0.008). ( B ) Analysis of EBOV titer changes in cells of various passages. The arrows point out data from passages plotted in (A).

    Article Snippet: In general, there did not appear to be a noticeable trend indicating any decrease in viral titer measured in the BEI Vero E6 cells, but there may be a slight trend in decrease of titer over time in the ATCC Vero E6 cells.

    Techniques:

    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Journal: The Journal of Biological Chemistry

    Article Title: Identification of Critical Amino Acids within the Nucleoprotein of Tacaribe Virus Important for Anti-interferon Activity *

    doi: 10.1074/jbc.M112.444760

    Figure Lengend Snippet: Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Article Snippet: The TCRV NP clone sequence for BEI resources stock used in this paper has been deposited in GenBank (accession no. ).

    Techniques: Activity Assay, Sequencing, Derivative Assay, Expressing, Infection, Transfection, Molecular Weight, Purification, Plasmid Preparation, Activation Assay, Positive Control

    Filovirus plaques produced on Vero E6 cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on BEI Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.

    Journal: Viruses

    Article Title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies

    doi: 10.3390/v4123511

    Figure Lengend Snippet: Filovirus plaques produced on Vero E6 cells from two sources are similar in appearance and titer. ( A ) EBOV plaques on ATCC Vero E6 cells plated at (1) 24 hours before assay, and (2) 72 hours before assay. EBOV plaques on BEI Vero E6 cells plated at (3) 24 hours before assay, and (4) 72 hours before assay. (5) MARV plaques on Vero cells from (5) ATCC and (6) BEI plated 24 hours before assay. ( B ) EBOV titers are similar in Vero E6 cells from ATCC and BEI when measured independently by two operators. This experiment was performed twice with up to 3 operators (data not shown), and one representative graph is shown. Each bar represents an average of 7 replicates.

    Article Snippet: Vero E6 cells from ATCC are available for purchase, but Vero E6 cells from BEI Resources, a NIAID-funded, ATCC-managed repository can be obtained free of charge in support of government funded projects, making them attractive for use in standardized assays.

    Techniques: Produced

    Vero E6 cells are suitable for quantitation of EBOV plaques. ( A ) Vero and Vero E6 cells produce EBOV plaques. ( B ) EBOV titers are similar in ATCC Vero E6 cells plated 24, 48 or 72 hours prior to plaque assay. This experiment was performed twice, and one representative graph is shown. Each bar represents an average of 5 replicates. The * indicates p = 0.006 between 24 and 72 hour samples for passage 29.

    Journal: Viruses

    Article Title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies

    doi: 10.3390/v4123511

    Figure Lengend Snippet: Vero E6 cells are suitable for quantitation of EBOV plaques. ( A ) Vero and Vero E6 cells produce EBOV plaques. ( B ) EBOV titers are similar in ATCC Vero E6 cells plated 24, 48 or 72 hours prior to plaque assay. This experiment was performed twice, and one representative graph is shown. Each bar represents an average of 5 replicates. The * indicates p = 0.006 between 24 and 72 hour samples for passage 29.

    Article Snippet: Vero E6 cells from ATCC are available for purchase, but Vero E6 cells from BEI Resources, a NIAID-funded, ATCC-managed repository can be obtained free of charge in support of government funded projects, making them attractive for use in standardized assays.

    Techniques: Quantitation Assay, Plaque Assay

    ( A ) EBOV titers in ATCC or BEI Vero E6 cells of various passage ages. This experiment was performed by three independent investigators, four replicates per cell type. The combined data are presented, where each bar represents 12 replicates. * indicates a significant difference in value between BEI passage 40 and passage 27 ( p = 0.0003), ** a difference between ATCC passage 54 and 28 ( p = 0.007), and *** a difference between BEI passage 40 and ATCC passage 28 ( p = 0.000002). For these experiments, p value cutoff was ≤0.008). ( B ) Analysis of EBOV titer changes in cells of various passages. The arrows point out data from passages plotted in (A).

    Journal: Viruses

    Article Title: Standardization of the Filovirus Plaque Assay for Use in Preclinical Studies

    doi: 10.3390/v4123511

    Figure Lengend Snippet: ( A ) EBOV titers in ATCC or BEI Vero E6 cells of various passage ages. This experiment was performed by three independent investigators, four replicates per cell type. The combined data are presented, where each bar represents 12 replicates. * indicates a significant difference in value between BEI passage 40 and passage 27 ( p = 0.0003), ** a difference between ATCC passage 54 and 28 ( p = 0.007), and *** a difference between BEI passage 40 and ATCC passage 28 ( p = 0.000002). For these experiments, p value cutoff was ≤0.008). ( B ) Analysis of EBOV titer changes in cells of various passages. The arrows point out data from passages plotted in (A).

    Article Snippet: Vero E6 cells from ATCC are available for purchase, but Vero E6 cells from BEI Resources, a NIAID-funded, ATCC-managed repository can be obtained free of charge in support of government funded projects, making them attractive for use in standardized assays.

    Techniques:

    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Journal: The Journal of Biological Chemistry

    Article Title: Identification of Critical Amino Acids within the Nucleoprotein of Tacaribe Virus Important for Anti-interferon Activity *

    doi: 10.1074/jbc.M112.444760

    Figure Lengend Snippet: Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Article Snippet: Although the reference sequence, BEI resources, and ATCC TCRV stocks are all derived from strain 11573, variation in sequences may have occurred due to different methods or duration of passaging in cell culture.

    Techniques: Activity Assay, Sequencing, Derivative Assay, Expressing, Infection, Transfection, Molecular Weight, Purification, Plasmid Preparation, Activation Assay, Positive Control

    Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Journal: The Journal of Biological Chemistry

    Article Title: Identification of Critical Amino Acids within the Nucleoprotein of Tacaribe Virus Important for Anti-interferon Activity *

    doi: 10.1074/jbc.M112.444760

    Figure Lengend Snippet: Analysis of a TCRV NP with GPPT residues important for anti-IFN activity. A , alignment of protein sequences near the DLQL peptide stretch of the TCRV NP reference sequence ( REF ) to the sequences derived from BEI resources ( BEI ) and ATCC TCRV viral stocks. B–D , measurements of IFNβ reporter activity during expression of codon-optimized (reference sequence) TCRV NP with the DLQL sequence (TCRV NP) or containing GPPT in place of the DLQL residues (TNP-GPPT). Induction of the IFNβ promoter was performed by infection with SeV ( B ), transfection with 10 μg/ml low molecular weight poly(I:C) ( C ), or with 250 ng of purified TCRV RNA ( D ) following methods described under “Experimental Procedures.” E , increasing amounts of the vTNP, TNP-GPPT, and PICV NP ranging from 0.1 and 1 μg of plasmid DNA were transfected into 293T cells and subjected to the IFN activation assay explained under “Experimental Procedures.” The positive control was set as 100% activation, and the rest of the conditions were normalized to this value. Shown are the means of three experiments performed in triplicate (**, p

    Article Snippet: The BEI TCRV stock was derived from tissue culture (Vero) infection, whereas the ATCC TCRV stock was prepared from a newborn mouse brain inoculation.

    Techniques: Activity Assay, Sequencing, Derivative Assay, Expressing, Infection, Transfection, Molecular Weight, Purification, Plasmid Preparation, Activation Assay, Positive Control

    The 50% lethal dose of B. mallei ATCC 23344 when administered by oropharyngeal aspiration. Five doses of 10-fold serial dilutions were prepared to administer 3.8×10 5 cfu, 3.6×10 4 cfu, 3.36×10 3 cfu, 366 cfu and 36 cfu of B. mallei ATCC 23344 to BALB/c mice by OA as described as described in the materials and methods and Fig. 1 . Mice were observed for 14 days. The actual inhaled doses are shown in the graph and were utilized to calculate LD 50 (1.7×10 3 cfu).

    Journal: PLoS ONE

    Article Title: Oropharyngeal Aspiration of Burkholderia mallei and Burkholderia pseudomallei in BALB/c Mice

    doi: 10.1371/journal.pone.0115066

    Figure Lengend Snippet: The 50% lethal dose of B. mallei ATCC 23344 when administered by oropharyngeal aspiration. Five doses of 10-fold serial dilutions were prepared to administer 3.8×10 5 cfu, 3.6×10 4 cfu, 3.36×10 3 cfu, 366 cfu and 36 cfu of B. mallei ATCC 23344 to BALB/c mice by OA as described as described in the materials and methods and Fig. 1 . Mice were observed for 14 days. The actual inhaled doses are shown in the graph and were utilized to calculate LD 50 (1.7×10 3 cfu).

    Article Snippet: Bacterial Strains and Challenge Dose Preparation B. pseudomallei K96243 and B. mallei ATCC 23344 were obtained from BEI Resources and stored at −80°C in single use aliquots.

    Techniques: Mouse Assay