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Human ubiquitin c promoter

Manufactured by Jackson ImmunoResearch

The Human ubiquitin C promoter is a DNA regulatory sequence that drives the expression of the ubiquitin C gene in human cells. It is commonly used to achieve constitutive or ubiquitous expression of target genes in various applications.

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3 protocols using human ubiquitin c promoter

1

Transgenic Mice for Immune Studies

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FcγRIIb-deficient mice on a C57BL/6 background18 (link) were kindly provided by Jeff Ravetch (Rockefeller University, New York) and Silvia Bolland (National Institutes of Health, NIAID, Bethesda, MD) and crossed to transgenic mice expressing EGFP under the control of the human ubiquitin C promoter38 (Jackson Laboratories) or transgenic mice expressing Venus EYFP under the control of the CD11c promoter39 (obtained from M. Nussenzweig, Rockefeller University, New York, NY). C57BL/6 mice were obtained from Jackson Laboratories or from Charles River Laboratories (Margate, UK). NZB/W F1 were bred in-house from NZB and NZW mice obtained from Harlan UK. CCR7-deficient mice on a C57BL/6 background (strain B6.129P2(C)-Ccr7tm1Rfor/J, stock number 006621, live repository, aged 8 weeks old) were purchased from Jackson Laboratories. Age matched C57BL/6 JAX mice were used as controls. In all experiments, both male and female mice were used. Mice were maintained in specific-pathogen-free conditions at an Association for Assessment and Accreditation of Laboratory Animal Care-accredited animal facility at NIAID or at a Home Office-approved facility in the UK. All procedures were approved by the NIAID Animal Care and Use Committee (National Institutes of Health, Bethesda, MD) or were conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act 1986.
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2

Transgenic Mouse Models for Research

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Two-month-old virgin female BALB/c mice (Animal Facility, IBYME) were used. Transgenic mice expressing enhanced Green Fluorescent Protein (GFP) under the direction of the human ubiquitin C promoter (The Jackson Laboratories, Bar Harbor, Maine) were bred at IBYME (BALB/c-GFP). Nu/nu females were obtained from the University of La Plata and NOD/LtSz-scid/IL-2Rgamma null mice (NSG) from The Jackson Laboratory and bred at IBYME. Animal care and manipulation were in agreement with the Guide for the Care and Use of Laboratory Animals [45 ].
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3

Transgenic Mice for Immune Studies

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FcγRIIb-deficient mice on a C57BL/6 background18 (link) were kindly provided by Jeff Ravetch (Rockefeller University, New York) and Silvia Bolland (National Institutes of Health, NIAID, Bethesda, MD) and crossed to transgenic mice expressing EGFP under the control of the human ubiquitin C promoter38 (Jackson Laboratories) or transgenic mice expressing Venus EYFP under the control of the CD11c promoter39 (obtained from M. Nussenzweig, Rockefeller University, New York, NY). C57BL/6 mice were obtained from Jackson Laboratories or from Charles River Laboratories (Margate, UK). NZB/W F1 were bred in-house from NZB and NZW mice obtained from Harlan UK. CCR7-deficient mice on a C57BL/6 background (strain B6.129P2(C)-Ccr7tm1Rfor/J, stock number 006621, live repository, aged 8 weeks old) were purchased from Jackson Laboratories. Age matched C57BL/6 JAX mice were used as controls. In all experiments, both male and female mice were used. Mice were maintained in specific-pathogen-free conditions at an Association for Assessment and Accreditation of Laboratory Animal Care-accredited animal facility at NIAID or at a Home Office-approved facility in the UK. All procedures were approved by the NIAID Animal Care and Use Committee (National Institutes of Health, Bethesda, MD) or were conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act 1986.
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