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murine endothelial svec 4 10 cell line  (ATCC)


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    ATCC murine endothelial svec 4 10 cell line
    Murine Endothelial Svec 4 10 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 369 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+endothelial+cells+svecs/us10358499-992-57-64?v=ATCC
    Average 96 stars, based on 369 article reviews
    murine endothelial svec 4 10 cell line - by Bioz Stars, 2026-07
    96/100 stars

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    96
    ATCC murine endothelial svec 4 10 cell line
    Murine Endothelial Svec 4 10 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+endothelial+cells+svecs/us10358499-992-57-64?v=ATCC
    Average 96 stars, based on 1 article reviews
    murine endothelial svec 4 10 cell line - by Bioz Stars, 2026-07
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    96
    ATCC murine endothelial cells svecs
    A: Kinetics of NO formation by murine <t>endothelial</t> cells <t>(SVECs)</t> treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). <t>CRL2181</t> cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).
    Murine Endothelial Cells Svecs, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC murine endothelial cell line svec 4 10
    A: Kinetics of NO formation by murine <t>endothelial</t> cells <t>(SVECs)</t> treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). <t>CRL2181</t> cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).
    Murine Endothelial Cell Line Svec 4 10, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+endothelial+cells+svecs/pm25781650-164-0-6?v=ATCC
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    ATCC murine svec endothelial cells
    A: Kinetics of NO formation by murine <t>endothelial</t> cells <t>(SVECs)</t> treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). <t>CRL2181</t> cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).
    Murine Svec Endothelial Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC c immortalized murine endothelial cell lines svec
    A: Kinetics of NO formation by murine <t>endothelial</t> cells <t>(SVECs)</t> treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). <t>CRL2181</t> cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).
    C Immortalized Murine Endothelial Cell Lines Svec, 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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    ATCC murine endothelial cells svec
    A: Kinetics of NO formation by murine <t>endothelial</t> cells <t>(SVECs)</t> treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). <t>CRL2181</t> cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).
    Murine Endothelial Cells Svec, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Johns Hopkins HealthCare svec-10 murine endothelial cell line
    A: Kinetics of NO formation by murine <t>endothelial</t> cells <t>(SVECs)</t> treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). <t>CRL2181</t> cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).
    Svec 10 Murine Endothelial Cell Line, supplied by Johns Hopkins HealthCare, 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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    A: Kinetics of NO formation by murine endothelial cells (SVECs) treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). CRL2181 cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).

    Journal: Journal of Lipid Research

    Article Title: Small dense HDLs display potent vasorelaxing activity, reflecting their elevated content of sphingosine-1-phosphate

    doi: 10.1194/jlr.M076927

    Figure Lengend Snippet: A: Kinetics of NO formation by murine endothelial cells (SVECs) treated with total HDL (50 μg protein per milliliter). B: NO formation by SVECs treated with total HDL and HDL3c (50 μg protein per milliliter) alone or in combination with the S1P receptor antagonist, VPC 23019 (VPC). CRL2181 cells were preincubated with VPC (10 μM) for 30 min before adding HDL. A fluorescent probe for NO [DAF-2DA (5 μM in DMSO)] was preincubated for 30 min with cells before adding HDL. The fluorescent intensity was recorded at the excitation wavelength of 485 nm and emission wavelength of 520 nm and presented as a percentage of baseline reading obtained at time 0 (F0) (A) or in the absence of HDL (F-control) (B). Data shown are means of four independent experiments. *P < 0.05 versus time 0 (A) or versus corresponding HDL in the absence of VPC (B).

    Article Snippet: NO production in endothelial cells Simian vacuolating virus 40 (SV40)-transformed murine endothelial cells (SVECs) (ATCC number: CRL2181) were cultured in DMEM supplemented with 10% FBS to sub-confluency.

    Techniques: Control