Ontology highlight
ABSTRACT:
INSTRUMENT(S): Orbitrap Fusion, Q Exactive
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Permanent Cell Line Cell, Cell Culture
SUBMITTER: Tina Beyer
LAB HEAD: Marius Ueffing
PROVIDER: PXD008343 | Pride | 2018-04-04
REPOSITORIES: Pride
Action | DRS | |||
---|---|---|---|---|
Cluap1isoform1.zip | Other | |||
Cluap1isoform3.zip | Other | |||
Cluap1isoform4.zip | Other | |||
IFT20_CluapKO.zip | Other | |||
TBE1995-S26-B-B79_1.raw | Raw |
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Molecular & cellular proteomics : MCP 20180403 7
CRISPR/Cas9-mediated gene editing allows manipulation of a gene of interest in its own chromosomal context. When applied to the analysis of protein interactions and in contrast to exogenous expression of a protein, this can be studied maintaining physiological stoichiometry, topology, and context. We have used CRISPR/Cas9-mediated genomic editing to investigate Cluap1/IFT38, a component of the intraflagellar transport complex B (IFT-B). Cluap1 has been implicated in human development as well as ...[more]