Protein Production
293FT, 293E, CHO

Truly Functional Protein
95% Purity
1-10 mg in 2 weeks

GeneExpressoMax™
293Expresso™

Transfection Reagents
* 90% Efficiency
* 95% Viability
* No sera interference
* Simple protocol
* High-throughput
* Only $98/ml

Baculovirus
Functional Protein
95% Purity
Fast turnaround
1-10 mg from Sf9 cells

Adenovirus, AAV
& Lentivirus

ORF or shRNA
* High Titer
* Cre, FLP, ΦC31
* Protein Kinases
* Transcription Factors
* Luciferases, GFP, RFP
* Protein Production
* Stable Cell Line


Excellgen

A SYSTEMATIC RNAI-BASED MAP OF C. ELEGANS EMBRYOGENESIS

C Kristin
New York Universitycity: New York    country: United States (us)

Grant 5R01HD046236-09 from Eunice Kennedy Shriver National Institute Of Child Health & Human Development

Keywords: ing; Address; Affect; Alleles; Architecture; Archives; Area; Award; base; Biological; Biological Assay; Biological Process; Biology; Budgets; Buffers; C. elegans genome; Caenorhabditis elegans; Cell division; Cell Polarity; Chromosome Mapping; Code; combinatorial; Complex; Data; Data Analyses; Data Collection; data integration; Databases; Development; Developmental Process; Disease; Educational process of instructing; Embryo; Embryonic Development; Enhancers; Ensure; Event; Evolution; experience; Fertilization; functional genomics; Funding; gene interaction; Genes; Genetic; genetic analysis; Genetic Models; Genetic screening method; Genome; genome sequencing; genome-wide; Goals; Human; human disease; Human Genome; Image; in vivo; insight; Kinetochores; Laboratories; Lead; Link; Maps; Meiosis; MEL Gene; Mitosis; Modeling; Molecular; Molecular Genetics; National Institute of Child Health and Human Development; Nuclear Envelope; Organism; Outcome; Pathway interactions; Pattern; Phenotype; Play; Process; Program Development; programs; Property; protein protein interaction; Proteins; Research; Resolution; RNA Interference; Role; scaffold; Staging; System; Testing; Time; tool; United States National Institutes of Health; Work; Yeasts

Project start date: 2003-12-01

Project end date: 2013-11-30

Budget start date: 1-DEC-2011

Budget end date: 30-NOV-2012

5R01HD046236-09 (2012): $490938


Sponsored Links Excellgen http://Excellgen.com

Recombinant Lentivirus & Adenovirus
High Yield and High Titer up to 1010 (lentivirus) and 1013 (adenovirus) for Guaranteed Expression of GOI. $3000, $2500
Transient Protein Expression in CHO and HEK293 Cells
Transient Expression, Truly Functional Protein, 95% purity, 1~20 mg, fast turnaround. $5500, $3950
Baculovirus Protein Expression
Fast turn around, >95% purity functional protein. No outsourcing to China or India. $5500, $3950


Grants awarded to C Kristin

A SYSTEMS BIOLOGY APPROACH TO MAMMALIAN EARLY EMBRYOGENESIS

C Kristin, Research Assistant Professor
New York Universitycity: New York    country: United States (us)

Grant 5R01GM085503-04 from National Institute Of General Medical Sciences

Abstract: It is now becoming clear that heritable and acquired human disorders arise from a complex interplay between multiple genetic components influenced by environmental factors. Therefore, scanning the genome for genetic associations to a specific disease is hampered by the fact that different individuals with the same disease could have different underlying genetic causes. When associations are found, they are often weak or relate to only one population of individuals sharing a particular genetic history. To alleviate this limitation we need a broader view of the molecular assemblages that specify particular phenotypes and need to develop better systems for the analysis of complex phenotypes. Disease phenotypes, especially for the most significant diseases, like cancer, are often the result of a breakdown in a basic cellular or developmental process. Thus, in the long term, this project aims to build a systems view of the molecular mechanisms driving these basic processes and use this information to inform the analysis of genome wide association studies. To begin this process we will build a systems view of early embryogenesis in mouse and human and connect them to specific phenotypic outcomes underlying basic cell and developmental processes. This approach has been very successful in the model C. elegant, where groups of genes required for specific phenotypes were identified on a genome-wide scale. We will use similar computational and experimental approaches as well as use a compendium of data from several model systems to build a systems view of early embryonic development in mouse and human. Specifically we will work on the following three related aims 1 Develop a computational framework to predict the global molecular map underlying early embryonic development in mouse and human. 2 Gather high-content phenotypic data during early embryogenesis using RNAi of ~400 mouse genes; digitally encode their complex phenotypic effect and combine with transcriptome data and the computational map built in Aim 1. 3 Develop an open-access Web-environment to navigate and analyze these complex data, including time-lapse recordings of early embryonic phenotypes so that they can be used to analyze genome-wide associations´ studies. This work will have direct implications for diagnosis of embryonic viability in a clinical setting and, due to the pleiotropic roles of many genes, will in turn provide insights into complex phenotypes associated with a variety of developmental and metabolic disorders as well as other disease processes like cancer, which involves deregulation of cell proliferation vs. differentiation

Keywords: Automobile Driving; Basic Science; Biological Models; Biological Process; blastocyst; Caenorhabditis elegans; Cell physiology; Cell Proliferation; Cells; Clinical; clinical Diagnosis; Clinical Research; Clinical Treatment; Comparative Study; Competence; Complex; computer framework; Couples; Data; Data Set; Development; developmental disease/disorder; Developmental Process; Diagnosis; Disease; disease phenotype; Embryo; Embryonic Development; Environment; Environmental Risk Factor; Event; experience; Foundations; Gene Components; Gene Expression; Gene Expression Profile; Genes; Genetic; genetic association; Genome; Genome Scan; genome wide association study; genome-wide; Goals; Hereditary Disease; Human; human DICER1 protein; Image; Individual; Infertility; insight; Internet; Invertebrates; Life; Link; Malignant Neoplasms; Mammals; Maps; Metabolic Diseases; MicroRNAs; Microscopy; Modeling; Molecular; Molecular Analysis; molecular phenotype; Molecular Profiling; Mus; Outcome; phenomics; Phenotype; Population; Post-Transcriptional Regulation; predictive modeling; Process; Property; protein protein interaction; Proteins; Protocols documentation; Recording of previous events; Resolution; Resources; RNA Interference; Role; spatiotemporal; Specific qualifier value; Staging; System; Systems Analysis; Systems Biology; Time; time use; Tissues; tool; Translating; Work

Relevance: 7. Narrative Many developmental abnormalities and diseases are caused by errors in how different biological processes are coordinated. This project aims to produce a first-draft map of how functional modules are coordinated in early embryogenesis in mammals, including humans. This will help us understand a broad array of normal and disease mechanisms, since many of the same modules operate in many different tissues and times in development; an immediate clinical benefit will be to provide better data to help diagnose the developmental competence of preimplantation embryos, thus helping many couples with infertility problems

Project start date: 2008-09-01

Project end date: 2012-08-31

Budget start date: 1-SEP-2011

Budget end date: 31-AUG-2012

PFA/PA: RFA-GM-08-001

5R01GM085503-04 (2011): $378065


5R01GM085503-03 (2010): $369037

5R01GM085503-02 (2009): $370927

1R01GM085503-01 (0000): $355294