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sindbis virus sinv  (ATCC)


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    Structured Review

    ATCC sindbis virus sinv
    Sindbis Virus Sinv, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 102 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sindbis virus sinv/product/ATCC
    Average 94 stars, based on 102 article reviews
    sindbis virus sinv - by Bioz Stars, 2026-06
    94/100 stars

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    94
    ATCC sindbis virus sinv
    Sindbis Virus Sinv, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    sinv  (ATCC)
    92
    ATCC sinv
    Sinv, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    ATCC sinv ar339 strain vr 1248
    Growth kinetics of Zambian SINV isolate M115 Vero (A) and BHK-21 (B) cells were infected with SINV isolate M115 and <t>AR339</t> at an MOI of 0.0001. C6/36 cells (C) were infected with SINV at an MOI of 0.01. Titers at the indicated each time point were determined by plaque assay. The values shown are mean ± standard deviation (SD) of triplicate. * p < 0.05, *** p < 0.001 by two-way ANOVA test.
    Sinv Ar339 Strain Vr 1248, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC sindbis virus sinv ar 339 strain
    Growth kinetics of Zambian SINV isolate M115 Vero (A) and BHK-21 (B) cells were infected with SINV isolate M115 and <t>AR339</t> at an MOI of 0.0001. C6/36 cells (C) were infected with SINV at an MOI of 0.01. Titers at the indicated each time point were determined by plaque assay. The values shown are mean ± standard deviation (SD) of triplicate. * p < 0.05, *** p < 0.001 by two-way ANOVA test.
    Sindbis Virus Sinv Ar 339 Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 95 stars, based on 1 article reviews
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    95
    ATCC sinv ar 339 strain
    Growth kinetics of Zambian SINV isolate M115 Vero (A) and BHK-21 (B) cells were infected with SINV isolate M115 and <t>AR339</t> at an MOI of 0.0001. C6/36 cells (C) were infected with SINV at an MOI of 0.01. Titers at the indicated each time point were determined by plaque assay. The values shown are mean ± standard deviation (SD) of triplicate. * p < 0.05, *** p < 0.001 by two-way ANOVA test.
    Sinv Ar 339 Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 95 stars, based on 1 article reviews
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    90
    Cold Spring Harbor Laboratory Meetings sindbis virus (sinv) barcode library
    A Workflow. The brain is injected with barcoded viral library. After 24–48 h of expression, during which RNA barcodes are transported to axon terminals, where they are amplified into rolonies and sequenced. B , C Single rolonies in axons have significantly weaker signals compared to somatic rolonies. B Representative image of somatic and axonal rolonies; dotted circle: somatic rolonies; arrow: axonal rolonies, with zoom-in views shown on the right; rolony intensity is color coded. Scale bar: 100 µm. C Quantification of intensity between axonal and somatic rolonies. Due to the large intensity difference between somatic and axonal rolonies, proper exposure for axonal rolonies often results in saturation of somatic rolonies. Paired t -test, two-tailed, p -value < 0.0001. D Representative images of axonal and somatic rolonies in AudC/I and ipsilateral thalamus. Images are from the first cycle of in situ sequencing. Similar results are observed across sections of the same brain regions. Dotted line, anatomical boundaries. Scale bar: top, 100 µm; bottom, 25 µm. E Registered <t>barcode</t> signals in CCFv3. Top, data in 3D model. Gray, brain outline. Bottom, coronal view of 25 µm of the sample. Gray, DAPI. F Representative images of in situ sequencing soma and a single axonal rolony with the same barcode. Soma ROI, 30.25 µm × 30.25 µm from injection site; axonal rolony ROI, 14.85 µm × 14.85 µm from ipsilateral thalamus. In total, 17 sequencing cycles are shown. G An example of tracing tracks for a single barcoded neuron reconstructed by connecting rolonies. Rolony location is indicated in white; soma location is indicated as a large green dot in ipsilateral cortex. AudC/I, contra/ipsilateral auditory cortex; Thal, thalamus; BC, barcode; D, dorsal; V, ventral; C, caudal; R, rostral; Seq, sequencing cycle.
    Sindbis Virus (Sinv) Barcode Library, supplied by Cold Spring Harbor Laboratory Meetings, 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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    Growth kinetics of Zambian SINV isolate M115 Vero (A) and BHK-21 (B) cells were infected with SINV isolate M115 and AR339 at an MOI of 0.0001. C6/36 cells (C) were infected with SINV at an MOI of 0.01. Titers at the indicated each time point were determined by plaque assay. The values shown are mean ± standard deviation (SD) of triplicate. * p < 0.05, *** p < 0.001 by two-way ANOVA test.

    Journal: Virus Research

    Article Title: Mosquito-borne alphaviruses in Zambia: Isolation and characterization of Eilat and Sindbis viruses

    doi: 10.1016/j.virusres.2025.199604

    Figure Lengend Snippet: Growth kinetics of Zambian SINV isolate M115 Vero (A) and BHK-21 (B) cells were infected with SINV isolate M115 and AR339 at an MOI of 0.0001. C6/36 cells (C) were infected with SINV at an MOI of 0.01. Titers at the indicated each time point were determined by plaque assay. The values shown are mean ± standard deviation (SD) of triplicate. * p < 0.05, *** p < 0.001 by two-way ANOVA test.

    Article Snippet: The SINV AR339 strain (VR-1248) was obtained from the ATCC.

    Techniques: Infection, Plaque Assay, Standard Deviation

    A Workflow. The brain is injected with barcoded viral library. After 24–48 h of expression, during which RNA barcodes are transported to axon terminals, where they are amplified into rolonies and sequenced. B , C Single rolonies in axons have significantly weaker signals compared to somatic rolonies. B Representative image of somatic and axonal rolonies; dotted circle: somatic rolonies; arrow: axonal rolonies, with zoom-in views shown on the right; rolony intensity is color coded. Scale bar: 100 µm. C Quantification of intensity between axonal and somatic rolonies. Due to the large intensity difference between somatic and axonal rolonies, proper exposure for axonal rolonies often results in saturation of somatic rolonies. Paired t -test, two-tailed, p -value < 0.0001. D Representative images of axonal and somatic rolonies in AudC/I and ipsilateral thalamus. Images are from the first cycle of in situ sequencing. Similar results are observed across sections of the same brain regions. Dotted line, anatomical boundaries. Scale bar: top, 100 µm; bottom, 25 µm. E Registered barcode signals in CCFv3. Top, data in 3D model. Gray, brain outline. Bottom, coronal view of 25 µm of the sample. Gray, DAPI. F Representative images of in situ sequencing soma and a single axonal rolony with the same barcode. Soma ROI, 30.25 µm × 30.25 µm from injection site; axonal rolony ROI, 14.85 µm × 14.85 µm from ipsilateral thalamus. In total, 17 sequencing cycles are shown. G An example of tracing tracks for a single barcoded neuron reconstructed by connecting rolonies. Rolony location is indicated in white; soma location is indicated as a large green dot in ipsilateral cortex. AudC/I, contra/ipsilateral auditory cortex; Thal, thalamus; BC, barcode; D, dorsal; V, ventral; C, caudal; R, rostral; Seq, sequencing cycle.

    Journal: Nature Communications

    Article Title: Massive multiplexing of spatially resolved single neuron projections with axonal BARseq

    doi: 10.1038/s41467-024-52756-x

    Figure Lengend Snippet: A Workflow. The brain is injected with barcoded viral library. After 24–48 h of expression, during which RNA barcodes are transported to axon terminals, where they are amplified into rolonies and sequenced. B , C Single rolonies in axons have significantly weaker signals compared to somatic rolonies. B Representative image of somatic and axonal rolonies; dotted circle: somatic rolonies; arrow: axonal rolonies, with zoom-in views shown on the right; rolony intensity is color coded. Scale bar: 100 µm. C Quantification of intensity between axonal and somatic rolonies. Due to the large intensity difference between somatic and axonal rolonies, proper exposure for axonal rolonies often results in saturation of somatic rolonies. Paired t -test, two-tailed, p -value < 0.0001. D Representative images of axonal and somatic rolonies in AudC/I and ipsilateral thalamus. Images are from the first cycle of in situ sequencing. Similar results are observed across sections of the same brain regions. Dotted line, anatomical boundaries. Scale bar: top, 100 µm; bottom, 25 µm. E Registered barcode signals in CCFv3. Top, data in 3D model. Gray, brain outline. Bottom, coronal view of 25 µm of the sample. Gray, DAPI. F Representative images of in situ sequencing soma and a single axonal rolony with the same barcode. Soma ROI, 30.25 µm × 30.25 µm from injection site; axonal rolony ROI, 14.85 µm × 14.85 µm from ipsilateral thalamus. In total, 17 sequencing cycles are shown. G An example of tracing tracks for a single barcoded neuron reconstructed by connecting rolonies. Rolony location is indicated in white; soma location is indicated as a large green dot in ipsilateral cortex. AudC/I, contra/ipsilateral auditory cortex; Thal, thalamus; BC, barcode; D, dorsal; V, ventral; C, caudal; R, rostral; Seq, sequencing cycle.

    Article Snippet: The sindbis virus (SINV) barcode library used in this study was generated by the MAPseq core facility at Cold Spring Harbor Laboratory.

    Techniques: Injection, Expressing, Amplification, Two Tailed Test, In Situ, Sequencing