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Gene Expression Data
Assay Details
Assay
Reference: J:307192 Yadav PS, et al., Stat3 loss in mesenchymal progenitors causes Job syndrome-like skeletal defects by reducing Wnt/beta-catenin signaling. Proc Natl Acad Sci U S A. 2021 Jun 29;118(26):e2020100118
Assay type: Western blot
MGI Accession ID: MGI:6831008
Gene symbol: Mmp13
Gene name: matrix metallopeptidase 13
Antibody: anti-Mmp13 (A1606)
Assay notes: Quantification of the Western blotting results in (F).
Results
Image: 2F Mmp13 ©

 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Genetic BackgroundMutant Allele(s)Sex Note
Prrx1Cre;Stat3C/+ P0 TS27: humerus Present involves: C57BL/6 * SJL/J Stat3tm1Flv/Stat3+, Tg(Prrx1-cre)1Cjt/0Not Specified Conditional mutant.
Prrx1Cre;Stat3C/+ P0 TS27: humerus Present involves: C57BL/6 * SJL/J Stat3tm1Flv/Stat3+, Tg(Prrx1-cre)1Cjt/0Not Specified Conditional mutant.
Prrx1Cre;Stat3C/C P0 TS27: humerus Weak involves: C57BL/6 * SJL/J Stat3tm1Flv/Stat3tm1Flv, Tg(Prrx1-cre)1Cjt/0Not Specified Conditional mutant.
Prrx1Cre;Stat3C/C P0 TS27: humerus Weak involves: C57BL/6 * SJL/J Stat3tm1Flv/Stat3tm1Flv, Tg(Prrx1-cre)1Cjt/0Not Specified Conditional mutant.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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03/18/2025
MGI 6.24 		The Jackson Laboratory