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PMID: 11121394
Takacs-Jarrett M, Sweeney WE, Avner ED, Cotton CU
Generation and phenotype of cell lines derived from CF and non-CF mice that carry the H-2K(b)-tsA58 transgene.
Am J Physiol Cell Physiol. 2001 Jan;280(1):C228-36.,
[PubMed]
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Comment
41
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:41:125
status:
NEW
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The goal of this work was to cross the ImmortoMouse (26) with the University of North Carolina (UNC) CF knockout mouse (CFTR
S489X
) (40) and develop genetically well-matched, conditionally immortalized CF and non-CF epithelial cell lines.
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42
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:42:230
status:
NEW
view ABCC7 p.Ser489* details
METHODS Animals Male mice, homozygous for a temperature-sensitive SV40 large T antigen transgene (ImmortoMouse; CBA/ca X C57B1/10 strain; Charles River Laboratories) (26), were bred with female mice that were heterozygous for the
S489X
CFTR mutation (UNC; CFTR ϩ/-; C57BL/6J X F129 strain) (40).
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50
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:50:41
status:
NEW
view ABCC7 p.Ser489* details
Primers 5 and 6 were used to amplify the
S489X
neodisrupted allele of CFTR (NEO).
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145
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:145:174
status:
NEW
view ABCC7 p.Ser489* details
The CF cell lines (mTEC1-CF, mCT1-CF, mSEC1-CF, and mPEC1-CF) were negative for the wild-type CFTR allele (faint 200-bp bands are non-CFTR PCR products) and positive for the
S489X
neodisrupted allele of CFTR.
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151
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:151:67
status:
NEW
view ABCC7 p.Ser489* details
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:151:203
status:
NEW
view ABCC7 p.Ser489* details
Magnification, ϫ270. both the wild-type CFTR allele and the
S489X
neodisrupted allele, whereas one of the non-CF cell lines (mSEC1) was positive for the wild-type CFTR allele and negative for the
S489X
neodisrupted allele of CFTR.
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179
ABCC7 p.Ser489*
X
ABCC7 p.Ser489* 11121394:179:89
status:
NEW
view ABCC7 p.Ser489* details
Wild-type cystic fibrosis transmembrane conductance regulator (CFTR), neomycin disrupted
S489X
CFTR (NEO), and Immorto (IM) alleles were identified from PCR products separated by gel electrophoresis.
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