型号：GM-J#006075 -Cryorecovery

应用：These knock-in mice were developed to utilize the mosaic analysis with double markers (MADM) system that allows simultaneous labeling and gene knockout in clones of somatic cells or isolated single cells in vivo. This strain carries the green fluorescent protein, EGFP (G), and the red fluorescent protein, Dsred2 (R), as markers to be used in conjunction with strains carrying the reciprocal chimeric marker genes (MADM-RG).

型号：GM-J#006071 -Cryorecovery

应用：These knock-in mice were developed to serve as controls for use with the mosaic analysis with double markers (MADM) system that allows simultaneous labeling and gene knockout in clones of somatic cells or isolated single cells in vivo. This strain carries only the green fluorescent protein, EGFP (G).

型号：GM-J#006067 -Cryorecovery

应用：These knock-in mice were developed to utilize the mosaic analysis with double markers (MADM) system that allows simultaneous labeling and gene knockout in clones of somatic cells or isolated single cells in vivo. This strain carries the red fluorescent protein, Dsred2 (R) and the green fluorescent protein, EGFP (G) as markers to be used in conjunction with strains carrying the reciprocal chimeric marker genes (MADM-GR).

型号：GM-J#006055 -Not Available At Jax

应用：These Z/RED transgenic mice express beta-galactosidase (lacZ) under the control of the chicken beta actin promoter coupled with the cytomegalovirus (CMV) immediate early enhancer. When crossed with a Cre recombinase-expressing strain, lacZ expression is replaced with red fluorescent protein (DsRed*MST) expression in tissues expressing Cre recombinase. This double reporter system makes it possible to distinguish a lack of reporter expression from a lack of Cre recombinase expression while providing a means to assess Cre excision activity in live animals and cells.

型号：GM-J#006054 -Available Now

应用：CMV-cre mice are useful for deletion of loxP-flanked genes in all tissues.

型号：GM-J#006053 -Cryorecovery

应用：These knock-in mice were developed to serve as controls for use with the mosaic analysis with double markers (MADM) system that allows simultaneous labeling and gene knockout in clones of somatic cells or isolated single cells in vivo. This strain carries only the green fluorescent protein, EGFP (G).

型号：GM-J#006041 -Cryorecovery

应用：These knock-in mice were developed to utilize the mosaic analysis with double markers (MADM) system that allows simultaneous labeling and gene knockout in clones of somatic cells or isolated single cells in vivo. This strain carries the green fluorescent protein, EGFP (G), and the red fluorescent protein, Dsred2 (R), as markers to be used in conjunction with strains carrying the reciprocal chimeric marker genes (MADM-RG).

型号：GM-J#005989 -Cryorecovery

应用：These PTH-cre mice express a transgene containing cre recombinase driven by the human PTH gene in parathyroid tissue.

型号：GM-J#005987 -Cryorecovery

应用：These Ache knock-out mice exhibit retarded growth, fine motor tremors, unusual posture and gait, no righting reflex, malformed pinna, and sealed eyelids.. They are suitable for studies of toxicology, neuromuscular junctions, nervous system function, neuropsychiatric diseases (Alzheimer's and Parkinson's), and blinding diseases (Retinitis pigmentosa and age-related macular degeneration).

型号：GM-J#005975 -Available

应用：These transgenic mice have a tamoxifen inducible Cre-mediated recombination system driven by the mouse Plp1, proteolipid protein (myelin) 1 promoter. When crossed with a strain containing a loxP site flanked sequence of interest, the offspring are useful for generating tamoxifen-induced, Cre-mediated targeted deletions. Tamoxifen administration allows for ablation of predetermined genes in oligodendrocytes and Schwann cells, and will also induce Cre recombination in developing embryos of treated mothers and in cultured cells derived from transgenic mice.