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3687 16411 Ensembl ENSG00000140678 ENSMUSG00000030789 UniProt P20702 Q9QXH4 RefSeq (mRNA) NM_000887 NM_001286375 NM_021334 NM_001363984 NM_001363985 RefSeq (protein) NP_000878 NP_001273304 NP_067309 NP_001350913 NP_001350914 Location (UCSC) Chr 16: 31.36 – 31.38 Mb Chr 7: 127.73 – 127.75 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse CD11c, also known as Integrin, alpha X ...
There are several thousand different strains of knockout mice. [3] Many mouse models are named after the gene that has been inactivated. For example, the p53 knockout mouse is named after the p53 gene which codes for a protein that normally suppresses the growth of tumours by arresting cell division and/or inducing apoptosis.
2660 17700 Ensembl ENSG00000138379 ENSMUSG00000026100 UniProt O14793 O08689 RefSeq (mRNA) NM_005259 NM_010834 RefSeq (protein) NP_005250 NP_034964 Location (UCSC) Chr 2: 190.06 – 190.06 Mb Chr 1: 53.1 – 53.11 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse In humans, the MSTN gene is located on the long (q) arm of chromosome 2 at position 32.2. Myostatin (also known as growth ...
A conditional gene knockout allows gene deletion in a tissue in a tissue specific manner. This is required in place of a gene knockout if the null mutation would lead to embryonic death, [13] or a specific tissue or cell type is of specific interest. This is done by introducing short sequences called loxP sites around the gene.
The International Knockout Mouse Consortium (IKMC) is a scientific endeavour to produce a collection of mouse embryonic stem cell lines that together lack every gene in the genome, and then to distribute the cells to scientific researchers to create knockout mice to study.
[23] [24] However it took another eight years before transgenic mice were developed that passed the transgene to their offspring. [25] [26] Genetically modified mice were created in 1984 that carried cloned oncogenes, predisposing them to developing cancer. [27] Mice with genes knocked out (knockout mouse) were created in 1989.
Gene knock-in originated as a slight modification of the original knockout technique developed by Martin Evans, Oliver Smithies, and Mario Capecchi.Traditionally, knock-in techniques have relied on homologous recombination to drive targeted gene replacement, although other methods using a transposon-mediated system to insert the target gene have been developed. [3]
In cell biology, CD11 is the α (alpha) component of various integrins, especially ones in which the β (beta) component is CD18 (β2) and mediate leukocyte adhesion. [1] ...
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