Ready-to-use, Pre-designed kits. Complete Kits for CRISPR App. Complete Kits for CRISPR App 1 Donor and 2 gRNA Pre-designed. Genome Edit Tools
- CRISPR Knockout
CRISPR Knockout
For every human and mouse gene
- CRISPR Service
Custom gRNA
7-10 days delivery
- Transgene Knockin
CRISPR AAVS1 and ROSA26
Robust and stable expression
- Robust Gene Expression
Experts in developing products for
pharmaceutical, biotechnology, ...
- Contact Us
Get in touch with us for more
information on OriGene products.
- For Antibody Validation
High Quality Antigen Standards! In
Stock
- CRISPR Knockout
Suchergebnisse
Suchergebnisse:
22. Apr. 2022 · By leveraging a large data set of genomes, in combination with phylogeny, travel history and date of sampling, this study estimates the number and sources of lineage introductions.
18. Mai 2020 · An accurate phylogenetic tree underpins our understanding of the major transitions in evolution, such as the emergence of new body plans or metabolism, and is key to inferring the...
- Paschalia Kapli, Ziheng Yang, Maximilian J Telford
- 2020
Genes, Genealogies and Phylogenies. Controversy over human evolution remains widespread. However, the Human Genome Project and genetic sequencing of many other species have provided myriad precise and unambiguous genetic markers that establish our evolutionary relationships with other mammals. Human Evolutionidentifi es and explains these ...
Human Evolution: Genes, Genealogies and Phylogenies identifies and explains these identifiable, rare and complex markers including endogenous retroviruses, genome-modifying transposable elements, gene-disabling mutations, segmental duplications and gene-enabling mutations.
- Graeme Finlay
- Paperback
3. Feb. 2020 · Here, we demonstrate PhaME’s ability to construct robust genus and species phylogenies using examples that span the tree of life, with up to thousands of genomes as input in the form of raw...
- Migun Shakya, Sanaa A. Ahmed, Karen W. Davenport, Mark C. Flynn, Chien-Chi Lo, Patrick S. G. Chain
- 2020
24. Feb. 2023 · We provide a protocol for information extraction from biological databases and simple phylogenetic reconstruction using probabilistic and distance methods, facilitating the study of biodiversity and evolution at the molecular level for the broad scientific community.
10. Aug. 2022 · Using fully sequenced genomes for orthology inference allows for a more confident assessment of gene histories by improving the detection of orthology and paralogy relationships, the estimation of gene gains and losses, and the detection of horizontal transfer events (see point 3).
We explain how genotyping by PCR, DNA microarrays and genotyping by sequencing work. Learn what genotyping is, what it is used for, and how the different methods work.
