CRISPR/Cas9 PlatformCB, a professional gene-editing technology services company, has extensive experience in the application of CRISPR/Cas gene-editing technology and has successfully knocked out/knocked specific genes in >300 mice. We guarantee to provide you with at least 2 Founder mice or 3 F1 mice and complete them within 3-5 months.
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CRISPR system is a novel tool for precise gene editing. Currently, the most commonly used system is derived from Streptococcus pyogenes (Sp), which consists of a Cas9 nuclease and a guide RNA. SpCas9 will induce a DNA double-stranded break after recruited to specific site by sgRNA. The subsequent homologous recombination repair will generate a knock-in or point mutation phenotype in the presence of a recombination donor. Thus, the HDR pathway are exploited to facilitate correction of diseased genes, insertion of epitope tags or fluorescent reporters, and overexpression of genes of interest in a site-specific manner.
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CRISPR/Cas9 PlatformCB is a professional genetic editing biotechnology company that provides transgenic mouse models for biomedical research and drug discovery. We will provide you with a one-stop-shop from experimental design strategies to successful mouse model generation. The CRISPR/Cas9 platformCB offers CRISPR-based knock-in mice at a very competitive price and complete in 3-4 months. We guarantee delivery of at least 2 founders or 3 F1 animals for knockin.
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CAR T cell therapy redirects patient T cells to target and eliminate tumor cells. CARs, fusion proteins with antibody-derived antigen recognition and T cell signaling domains, gained FDA approval in 2017 for CD19-targeted therapies in B-cell malignancies. Lentiviral vectors are crucial for CAR transduction in T cell manufacturing, offering stable integration and efficient transduction of dividing/nondividing cells. Creative Biogene provides a comprehensive line of CAR-T lentiviral particles, delivering ready-to-transduce CAR-T lentiviruses with up to 10^9 IFU/mL for accelerated research timelines.
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Luciferase Reporter Cell Line - A20 is engineered to stably overexpress luciferase reporter gene. It is an ideal positive control for use in bioluminescence assays. In addition, A20 cells form tumors post implantation into immunocompromised mice. The in vivo growth of these tumors can be monitored using bioluminescent imaging.
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GFP Reporter Cell Line is engineered to stably overexpress GFP reporter gene. MC38 is a murine colon carcinoma cell line, which has been widely used in laboratory research. This cell line is a useful tool for fluorescent tracking of MC38 cells.
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CRISPR/Cas9 PlatformCB utilizes CRISPR/Cas9 technology to generate custom genome-editing animal models for customers. Various species are available, including mouse, rat, zebrafish, C.elegans. CRISPR/Cas9 PlatformCB brings customer a wide range of genetic alterations service, including knockout, point mutations, short insertions, gene knock-in and conditional knock-in. In terms of experienced scientists, skilled staff and excellent platform, we provide one-stop custom animal models generation service with high success ratio.
https://www.creative-bioge...
CRISPR/Cas9 PlatformCB is a professional genetic editing biotechnology company that provides transgenic mouse models for biomedical research and drug discovery. We will provide you with a one-stop-shop from experimental design strategies to successful mouse model generation. The CRISPR/Cas9 platformCB offers CRISPR-based knock-in mice at a very competitive price and complete in 3-4 months. We guarantee delivery of at least 2 founders or 3 F1 animals for knockin.
https://www.creative-bioge...
CRISPR/Cas9 PlatformCB is a professional genetic editing biotechnology company that provides transgenic mouse models for biomedical research and drug discovery. We will provide you with a one-stop-shop from experimental design strategies to successful mouse model generation. The CRISPR/Cas9 platformCB offers CRISPR-based knock-in mice at a very competitive price and complete in 3-4 months. We guarantee delivery of at least 2 founders or 3 F1 animals for knockin.
https://www.creative-bioge...
Creative Biogene has established fully-matured RNAi system, ranges from design, siRNA synthesis/shRNA construction, transfection, expression evaluation to functional testing. On this basis, we offer cell-based RNAi service to verify the silencing effects of siRNA transient transfection and/or shRNA incorporation and stable expression. Creative Biogene has the ability to accurately evaluate the silencing activities of shRNA and siRNA, and assist you to screen shRNA/siRNA with high knockdown efficiency.
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Creative Biogene provides world-class MicroRNA (miRNA) sponge service and we have been perfecting MicroRNA sponge service for many years. Our microRNA sponge is a RNA molecule with 5-8 tandem miRNA binding sequences that can sequester miRNAs from their endogenous target mRNAs.
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Creative Biogene provides integrated solutions for your biosimilar projects. Our state-of-the-art facilities, the best scientists and technologies, regulatory expertise, combined with experience working with stable cell line generation and drug discovery, enable us to be an ideal partner to develop and deliver stable, high producing, functionally characterized biosimilar cell lines. It is important to demonstrate the comparability of a biosimilar to its corresponding reference product. We also possess robust expertise in performing comparibility analyses under non-GLP, GLP and GMP regulations.
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QVirus™ Platform offers a comprehensive portfolio of oncolytic VACV services for the efficient design, development, manufacturing and analytical testing of virus vector products. So far, we have developed an efficient way to generate recombinant VACVs, including inserting and/or deleting GOI(s) in VACVs. We also provide customized oncolytic vaccinia virus and proof-of-concept validation study for the oncolytic virus.
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Our QVirus™ platform can offer the packaging of your CRISPR libraries into our lentiviral vectors. CRISPR lentiviral libraries are packaged into highly pure and concentrated lentiviral particles, either from an existing lentiviral plasmid library or from a custom plasmid library that we construct starting from a provided oligonucleotide pool, corresponding to your guide sequences.
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Baculovirus Expression Vector System (BEVS) has become one of the recombinant protein expression systems most used in both, industry and molecular biology laboratories. BEVS has several advantages over other recombinant protein expression systems, including high protein yields, convenient use, biosafety and short development times. At present, the most widely used baculovirus expression system uses a lytic virus known as Autographa californica nuclear polyhedrosis virus (AcMNPV; hereafter called baculovirus). This virus is the prototype of the family Baculoviridae.
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Creative Biogene has established fully-matured RNAi system, ranges from design, siRNA synthesis/shRNA construction, transfection, expression evaluation to functional testing. On this basis, we offer cell-based RNAi service to verify the silencing effects of siRNA transient transfection and/or shRNA incorporation and stable expression. Creative Biogene has the ability to accurately evaluate the silencing activities of shRNA and siRNA, and assist you to screen shRNA/siRNA with high knockdown efficiency.
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Creative Biogene, as a leader in cell engineering, provides reliable, affordable, and fast knock-in cell line generation service, which includes gRNA/donor DNA construction, PCR sequencing, and engineered cell line generation. We have experience working with a wide variety of cell backgrounds ranging from easy-to-transfect cell lines (like HEK2993, HCT116 or HeLa) to hard-to-transfect cell lines (like iPSCs, fibroblasts). Creative Biogene produces knock-in cell lines and performs quality control testing in one step to help ensure that the cell line meets your requirements.
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Genomic engineering in cell lines is a versatile tool for studying gene function, designing diseases models, biopharmaceutical research, drug discovery and many other applications. CRISPR (Clustered Regulatory Interspaced Short Palindromic Repeats)/Cas9 systems is a newly developed yet the most popular method for genome editing. It has been widely used in current biology, functional genome screening, cell-based human hereditary disease modeling, epigenomic studies and visualization of cellular processes.
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Creative Biogene is a microbiotech company offering high-quality gene expression services in Bacillus for our esteemed clients around the world across both academic institutions and biotech/pharmaceutical industries. With our strong technical force, we specialize in providing more cost-effective gene expression services to accelerate the global research in microbial enzymes and recombinant proteins.
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Pseudomonas aeruginosa is a Gram-negative, rod-shaped bacterium known for its adaptability and versatility in various environments. Most Pseudomonas species are facultative anaerobes and use an inorganic compound such as nitrate as alternate terminal electron receptor. P. aeruginosa is capable of arginine fermentation and pyruvate fermentation. The organism produces the fluorescent siderophores pyoverdin and pyochelin, which function to scavenge iron. Redox-active phenazines such as pyocyanin, the pigment that gives P. aeruginosa its characteristic blue color, play an important role in electron transport especially under microaerophilic conditions, increase the bioavailability of iron, and enhance virulence through oxidative stress.
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Creative Biogene is a leading biotechnology company offering the best Salmonella genome editing services. With years of experience and expertise in microbial genome editing, our talented scientists will work closely with you to provide any help in Salmonella genome editing services.
Salmonella is the foodborne pathogen with the biggest public health and economic impact globally. It's one of the major causes of diarrhea all around the world, responsible for an estimated one million deaths and 100 million human infections annually. Genomic information decoded from a multitude of different Salmonella strains and new dramatic insights into pathogenic processes emphasize the fact that Salmonella research is currently at a very exciting juncture.
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