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Human Serous Endometrial Cancer Cell Lines CRISPR-edited to knock-in FBXW7 mutations for Use in Cancer related Molecular and Cellular Studies
Case ID:
TAB-3633
Web Published:
12/6/2022
Description:
This technology includes endometrial cancer cell lines for use in molecular and cellular studies to determine the effects of cancer-associated FBXW7 (F-box and WD repeat domain-containing 7) mutations, including but not limited to biochemical studies, proteomic studies, and drug sensitivity/resistance studies. Clustered Regularly Interspaced Palindromic Repeats (CRISPR) editing was used to knock-in individual FBXW7 mutations into the ARK1 serous EC cell line, which lacks detectable endogenous FBXW7 mutation(s). For each CRISPR-edited cell line, and parental ARK1 cells, STR (Short Tandem Repeat) profiles were generated. STR profiles of CRISPR-edited cell lines authenticated to the parental ARK1 line.
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Direct Link:
https://nih.technologypublisher.com/tech/Human_Serous_Endometrial_Cancer_Cell _Lines_CRISPR-edited_to_knock-in_FBXW7_mutations_for_Use_in_Cancer_related_M olecular_and_Cellular_Studies
Category(s):
Oncology
Therapeutics
Research Materials
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For Information, Contact:
Eggerton Campbell
Licensing And Patenting Manager
NIH Technology Transfer
301-402-1648
eggerton.campbell@nih.gov
Inventors:
Mary Urick
Daphne Bell
Keywords:
CANCER
Cell
CRISPR-edited
endometrial
FBXW7
Human
Knock-in
Lines
Mutations
Serous
VCXXXX
WIXXXX
XEXXXX
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