Rag1-KO(Rag1-EGFP)
Nomenclature
B6;129S-Rag1tm1(loxP-EGFP-PolyA-loxP-Neo-loxP)Smoc
Cat. NO.
NM-KI-00069
Strain State
Repository Live
Gene Summary
Gene Symbol
Rag1
Model Description
Validation Data
Fig.1 Construction strategy of Rag1-KO.
Fig.2 Loss of T and B cells in peripheral blood of Rag1-KO and Rag2-KO mice.
Fig.3 Loss of T and B cells in Spleen of Rag1-KO and Rag2-KO mice.
Fig.4 Loss of T and B cells in thymus of Rag1-KO and Rag2-KO mice.
Fig.5 Detection of mouse IgG(A) and IgM(B) expression in serum by ELISA. (male, 5~6wks, n=3)
Abbr. HO, homozygous; WT, wild type; N.D. not detected.
Fig.6 Tumorigenicity results following inoculation with A549 tumor cells in Balb/c nude, NOD-Scid, Rag1-KO and Rag2-KO mice.
Table1. Complete blood count of Rag1-KO (Rag1-EGFP) mice
Table 2. Serum biochemical analysis of Rag1-KO (Rag1-EGFP) mice.
Publications
Programmed death protein 1 is essential for maintaining the anti-inflammatory function of infiltrating regulatory T cells in a murine spinal cord injury model
References:Journal of Neuroimmunology
Peli1 negatively regulates noncanonical NF-κB signaling to restrain systemic lupus erythematosus
References:Nature Communications
Interleukin-17 Regulates Neuron-Glial Communications, Synaptic Transmission, and Neuropathic Pain after Chemotherapy
References:Cell Reports
Tpl2 Protects Against Fulminant Hepatitis Through Mobilization of Myeloid-Derived Suppressor Cells
References:Frontiers in Immunology
Gut Microbial Metabolite Pravastatin Attenuates Intestinal Ischemia/Reperfusion Injury Through Promoting IL-13 Release From Type II Innate Lymphoid Cells via IL-33/ST2 Signaling
References:Frontiers in Immunology
You may also like
On Dec 16, 2018, Broad Institute and Shanghai Model Organisms Center Inc (SMOC) has entered into a non-exclusive license agreement under which Broad has granted SMOC worldwide rights to commercialize a service platform for genetically modified mouse models under Broad's intellectual property.
Learn moreAt GenoBioTX, we understand that the lengthy wait times for gene-modified mouse models can hinder your research progress. Traditional methods often require 6-9 months, leading to delays and increased costs. That’s why we’re thrilled to introduce our innovative service designed to streamline this process and deliver results faster.
Learn more