grant

03 Genetically Engineered Mouse Facility

Organization UNIVERSITY OF TX MD ANDERSON CAN CTRLocation HOUSTON, UNITED STATESPosted 28 Aug 1996Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY2025AddressAmericanAnimal ModelAnimal Models and Related StudiesAnimalsAntioncogene Protein p53ArchivesAreaAwardBlastosphereBreedingBudgetsCCSGCRISPRCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas systemCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCancer CenterCancer Center Support GrantCapital FinancingCapital FundingCaringCas nuclease technologyCellular Tumor Antigen P53Clustered Regularly Interspaced Short Palindromic RepeatsClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCommunitiesCompensationConsultationsCryofixationCryopreservationDNADNA mutationDeoxyribonucleic AcidDerivationDerivation procedureDetectionDevelopmentE-learningES Cell LineES cellEducational process of instructingEducational workshopElectroporationEmbryoEmbryonicEmbryonic Stem Cell LineEndocrine Gland SecretionEquipmentFacultyFertilization in VitroFundingGEM modelGEMM modelGene ModifiedGene TargetingGene TranscriptionGene Transfer TechniquesGenerationsGenesGeneticGenetic ChangeGenetic EngineeringGenetic Engineering BiotechnologyGenetic Engineering Molecular BiologyGenetic TranscriptionGenetic defectGenetic mutationGenetically Engineered MouseGrantHormonesHuman ResourcesIn VitroInjectionsInstitutionInvestigatorsInvestmentsJapanJournalsKnock-inKnock-outKnockoutKnowledgeLaboratory Animal ScienceLacZLacZ GenesLibrariesLinkMagazineManpowerMediatingMethodologyMiceMice MammalsMicroscopeMissionModelingMouse ES CellMouse ESCMouse Embryonic ProgenitorMouse Embryonic Stem CellsMurineMusMutationOncoprotein p53OocytesOvocytesP53PaperPeer ReviewPhenotypePhosphoprotein P53Phosphoprotein pp53Preimplantation EmbryoProceduresProtein TP53ProtocolProtocols documentationPublicationsPublishingRNA ExpressionReagentRecombinant DNA TechnologyReproducibilityResearchResearch PersonnelResearch ResourcesResearchersResourcesScienceScientific PublicationServicesSpermSpermatozoaStem Cell DevelopmentSuperovulationSystemTP53TP53 geneTRP53TeachingTechniquesTest-Tube FertilizationTestingTexasTherapeutic HormoneTrainingTranscriptionTransgenesisTransgenic MiceTransgenic ModelTransgenic OrganismsTumor Protein p53Tumor Protein p53 GeneUpdateWorkshopanimal careanimal facilityanimal resourceanti-cancer researchblastocystblastulacancer researchcold preservationcold storagecomputer-assisted instructioncomputer-based educationcomputer-based instructioncomputer-based learningcomputer-based trainingconditional mutantconditional mutationconsultationcostdevelopmentaldigital educationdigital learningeLearningelectronic learningelectroporative deliveryembryo derived stem cellembryonal stem cellsembryonic progenitorembryonic stem cellexperimentexperimental researchexperimental studyexperimentsgene electrotransfergene modificationgenetically engineeredgenetically engineered mouse modelgenetically engineered murine modelgenetically modifiedgenome mutationin vivoinnovateinnovationinnovativeinternet-assisted educationinternet-based trainingknockinmESCmembermodel of animalmouse geneticsmouse modelmultimedia learningmurine ES cellsmurine ESCmurine embryonic progenitormurine embryonic stem cellmurine modelnew technologynovel technologieson-line educationon-line learningonline educationonline learningp53 Antigenp53 Genesp53 Tumor Suppressorpersonnelplasmid DNApre-implantation embryoprogenitor cell developmentprogenitor developmentprogramsprotein p53sperm cellstem and progenitor cell developmentstem cell approachstem cell based approachstem cell methodstem cell methodologystem cell of embryonic originstem cell procedurestem cell techniquetechnology-enhanced learningtransgenictransgenic traittumorvirtual learningweb-based instructionweb-based trainingwebinarzoosperm
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Full Description

PROJECT SUMMARY: GENETICALLY ENGINEERED MOUSE FACILITY (GEMF)
The MD Anderson Genetically Engineered Mouse Facility (GEMF) provides a wide range of mouse genetic

engineering services to investigators at a reasonable cost. Compensated services provided include transgenic

mouse generation (using pronuclear and blastocyst injection), gene targeting (using CRISPR/Cas9,

transposon-mediated transgenesis, the electroporation of embryonic stem [ES] cells, and TARGATT@

protocols), archiving of mouse embryos and sperm, generation of ES cells from investigators' own mouse

lines, and rederivation of mouse lines. In addition, consultation for assessing how genetically engineered

animals can contribute to PIs' projects and grant support are provided at no cost. A service unique to the

GEMF is the inclusion of a Mouse Resource Facility to provide reagents (e.g., superovulation hormones, ES

cell media), DNA plasmids (required for generating DNA constructs for gene targeting and pronuclear

injection), and Cre, LacZ, GFP, and p53 transgenic mice (commonly used for the detection and/or generation

of conditional mutations in mice and for probing tumor phenotypes). Support provided through CCSG

Development Funds was essential for developing the new GEMF service of in vitro transcription of sgRNA. The

facility has been in service since 1988 and was started by Dr. Guillermina Lozano, who was appointed

director in 2013, and is currently managed by Dr. Jan Parker-Thornburg, the co-director, who is a recipient of

an R50 award. The facility has an annual budget of $775,887 (74% for costs for highly expert personnel),

$342,039 (44%) of which is supported with CCSG funding. During the present grant period, the institution

invested $292,586 in funding for capital equipment, including replacement microscopes, automated injection

systems, and a multi-functional electroporation system that can be used both for ES cells and for

CRISPR/Cas9 embryo electroporation. Services provided have been fairly evenly distributed among

investigators at MD Anderson; 155 cancer center members representing all 16 CCSG programs have used

GEMF services over the past 6 years. In grant Yr42, peer-reviewed funding–supported usage accounted for

95% of all usage, and CCSG funds are requested to cover 41% of total expenses in Yr44 ($316,563). The

animals and materials produced by the GEMF have contributed significantly to high-impact science at MD

Anderson that has resulted in more than 201 publications, including 69 (34%) in journals with IF >10 and 146

(73%) in journals with IF >5. The GEMF's specific aims are: Aim 1. To produce the genetically engineered

animal models required by MD Anderson investigators for their studies in cancer research using both

traditional and state-of-the-art techniques, based on the need of the faculty. Aim 2. To provide services to MD

Anderson investigators to derive and archive mouse models. Aim 3. To use investigator-produced mouse

embryos for the generation of unique ES cell lines. Aim 4. To provide expertise and training in the generation,

care, and handling of GEM models.

Grant Number: 5P30CA016672-49
NIH Institute/Center: NIH

Principal Investigator: Fernando Benavides

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