HCT116 — IGVFSM9117BTSA

released

Summary

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin F for 80-100% expression of KITLG) modified with a guide library

Sample Terms

HCT116

Classification

cell line

Sex

male

Age

unknown

Construct Library Sets

IGVFDS7846UISG Guide (sgRNA) library targeting accessible genome regions in many genomic loci

Taxa

Homo sapiens

Sources

atcc

Sorted From Sample

IGVFSM4493UPPK FACS bin F for 80-100% expression of KITLG

Aliases

jesse-engreitz:in-vitro-system_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR1_S6

jesse-engreitz:in-vitro-system_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR2_S12

jesse-engreitz:in-vitro-system_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR3_S102

jesse-engreitz:in-vitro-system_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR4_S108

Donors

1 item

Accession

Aliases

Sex

Taxa

IGVFDO0384OZRW

igvf:donor_of_HCT116

male

Homo sapiens

File Sets

3 items

IGVFDS7789CCCR

CRISPR interference FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci

jesse-engreitz:measurement_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR1_S6
jesse-engreitz:measurement_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR2_S12
jesse-engreitz:measurement_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR3_S102
jesse-engreitz:measurement_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR4_S108

Jesse Engreitz, Stanford

IGVFDS8772YTOP

gRNA sequencing for CRISPR interference FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci

jesse-engreitz:auxiliary_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR1_S6
jesse-engreitz:auxiliary_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR2_S12
jesse-engreitz:auxiliary_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR3_S102
jesse-engreitz:auxiliary_CRUDO_KITLG-Auxin0hrs-FF1-BinF-PCR4_S108

Jesse Engreitz, Stanford

IGVFDS9621FJCZ

cell sorting for CRISPR interference FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci, CRISPR interference FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci, ... and 4 more measurement sets