型号:GM-J#037882 -Available
应用:CRISPR-generated Slc6a2-p2a-Cre knock-in mice express cre recombinase from the mouse solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 (Slc6a2) promoter. This strain has been useful in studies of area postrema excitatory neurons as they relate to nausea-associated behaviors.
型号:GM-J#037843 -Cryorecovery
应用:Exon 3 of the mouse Agpat5 (1-acylglycerol-3-phosphate O-acyltransferase 5 (lysophosphatidic acid acyltransferase, epsilon) gene is flanked by lox2272/loxP sites in these Agpat5flox mice. Cre recombinase-mediated excision of the floxed region results in a knock-out allele and expression of a tdTomato reporter useful in studies of agouti-related peptide neurons and their roles in insulin-induced hypoglycemia sensing and glucagon secretion.
型号:GM-J#037804 -Available
应用:Clec9aCreERT2 knock-in mice have a P2A peptide fused to a cre/ERT2 sequence inserted into the C-terminal of the Clec9a gene. This strain is useful for dendritic cell lineage fate mapping and for studying adaptive immune responses to antigens in apoptotic and necrotic cells.
型号:GM-J#037803 -Available
应用:KbStrep knock-in mice have an inverted StrepTagII, flanked by two pairs of inward-facing heterospecific Lox sites, inserted into intron 1 of the H2-K1 gene. Upon cre induction, recombination of the Lox sites results in the inversion of the StrepTagII into the correct transcriptional orientation. These mice may be useful for the selective purification of MHC-I peptide antigens from cell type(s) of interest from intact tissues.
型号:GM-J#037801-JAX -Cryorecovery
应用:The PAC-Tg(SNCAWT);Snca-/-; Gba1L444P/+ mice harbor a Snca knockout allele, a transgene encoding human alpha-synuclein and the L444P mutation in the Gba1 (glucosidase, beta, acid 1) gene associated with the alpha-synucleinopathy, Gaucher disease. This strain serves as an experimental control for STOCK Gba1tm1Rlp Sncatm1Nbm Tg(SNCA*A53T)1Nbm Tg(SNCA*A53T)2Nbm/Mmjax (MMRRC Stock Number 036733).
型号:GM-J#037719 -Available
应用:TIGRE2-jGCaMP8s-IRES-tTA2 knock-in mice co-express the jGCaMP8s genetically encoded calcium indicator (GECI) and a tetracycline controlled tetracycline controlled transactivator (tTA2) in a Cre recombinase-dependent manner from the intergenic Igs7 (TIGRE) locus. The addition of an internal ribosome entry site (IRES) introduced upstream of tTA and the omission of a WPRE enhancer element downstream ameliorate previously reported tTA overexpression toxicity issues. jGCaMP8s is a fast rise, medium decay green fluorescent-based GECI with improved sensitivity and faster kinetics.
型号:GM-J#037718 -Available
应用:TIGRE2-jGCaMP8m-IRES-tTA2-WPRE knock-in mice co-express the jGCaMP8m genetically encoded calcium indicator (GECI) and a tetracycline controlled transactivator (tTA2) in a Cre recombinase-dependent manner from the intergenic Igs7 (TIGRE) locus. An internal ribosome entry site (IRES) introduced upstream of tTA ameliorates previously reported tTA overexpression toxicity issues. jGCaMP8m is noted for its faster decay rate and offers a useful compromise between sensitivity and kinetics.
型号:GM-J#037702 -Cryorecovery
应用:FAC (FLPo-dependent Adipoq-Cre) knock-in mice express a FLPo-inducible Cre recombinase under the control of the Adipoq (adiponectin, C1Q and collagen domain containing) endogenous promoter. Following FLPo-mediated recombination cre is expressed in adipose tissue. This strain may be used in studies of bone marrow adipocytes and bone homeostasis.
型号:GM-J#037698 -Cryorecovery
应用:Cre-iPEEL mice enable widespread Cre recombinase-gated expression of hemagglutinin (HA)-tagged, plasma membrane-targeted, extracellularly-facing horseradish peroxidase (HRP), allowing for proximity labeling, biochemical capture, and proteomic profiling of cell-surface proteins in a cell-type-specific manner.
型号:GM-J#037697 -Cryorecovery
应用:Dual-iPEEL mice enable widespread Cre and Flp recombinase-gated expression of hemagglutinin (HA)-tagged, plasma membrane-targeted, extracellularly-facing horseradish peroxidase (HRP), allowing for proximity labeling, biochemical capture, and proteomic profiling of cell-surface proteins in a cell-type-specific manner.