CAP1 Stable Knockdown PANC-1 Cell Line

T64041x106 cells / 1.0 ml


DescriptionCAP1 mediate extracellular signals to control cancer cell invasiveness. Using two shRNA constructs S2 and S3 that target independent nucleotide sequences and effectively silenced CAP1 in HeLa and breast cancer cells we were able to generate stable clones with efficient CAP1 knockdown in the PANC-1 and AsPC-1 cells as confirmed in Western blotting. Knockdown of CAP1 in cancer cells led to enhanced stress fibers as well as reduced cell motility and invasion into Matrigel. These cells can be used to investigated roles for CAP1 and its phosphor-regulation in pancreatic cancer cells.
SpeciesHuman (H. sapiens)
Tissue/Organ/Organ SystemPancreas
Cell MorphologyEpithelial

For Research Use Only

Seeding Density20,000 - 30,000 cells/cm2
Population Doubling Time31 - 41 hours
Donor GenderMale
Donor GenderMale
Donor Age56
Donor DiseasePancreatic cancer
Donor EthnicityCaucasian
Immortalization MethodN/A
Cell TypeDrug Discovery Cell Lines
Growth PropertiesAdherent
Expression Profile

PANC-1 (clone S3-3) Drug resistance: 250 ug/ml neomycin Vector information: pRNA-U6.1/Neo vector was used S2 targets nucleotide 519-537 of human CAP1 gene; S3 targets nucleotides 1074-1092 of human CAP1 gene.

Preservation Protocol1. Freeze Medium: Complete growth medium with 20% FBS and 10% DMSO.
2. Storage Temperature: Liquid nitrogen vapour phase.
Unit quantity1x106 cells / 1.0 ml

1) Western blot


Supporting Protocol




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