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huTSLP/hTSLPR Mouse
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huTSLP/hTSLPR Mouse
Product Name
huTSLP/hTSLPR Mouse
Product ID
C001991
Strain Name
C57BL/6NCya-Tslpem1(hTSLP)Crlf2tm1(hCRLF2)/Cya
Backgroud
C57BL/6NCya
Status
Live Mouse
When using this mouse strain in a publication, please cite “huTSLP/hTSLPR Mouse (Catalog C001991) were purchased from Cyagen.”
HUGO-GT Humanized ModelsImmune Target Humanized Mouse ModelsCytokine Gene Humanized Mouse Models
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The standard delivery applies for a guaranteed minimum of three heterozygous carriers. Breeding services for homozygous carriers and/or specified sex are available.
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HUGO-GT Humanized ModelsImmune Target Humanized Mouse ModelsCytokine Gene Humanized Mouse Models
Basic Information
Related Resource
Basic Information
Gene Name
CRLF2 & TSLP
Gene Alias
CRL2, TSLPR, CRLF2Y
NCBI ID
64109 & 85480
Chromosome
Chr X, Chr 5
MGI ID
MGI:1855696; MGI:1889506
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Datasheet
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Strain Description
The huTSLP/hTSLPR mice are a dual-gene humanized model obtained by mating huTSLP mice (catalog No.: C001809) with hTSLPR mice (catalog No.: C001942). This model can be used for the mechanism research and treatment development of allergic diseases, inflammation, and autoimmune diseases, as well as the development of TSLP/TSLPR-targeted drugs.
Strain Strategy
The huTSLP/hTSLPR mice are a dual-gene humanized model obtained by mating huTSLP mice (catalog No.: C001809) with hTSLPR mice (catalog No.: C001942).
Figure 1. Gene editing strategy of huTSLP mice. The mouse Tslp endogenous domain was replaced with the human TSLP domain. The murine signal peptide was preserved.
Figure 1. Gene editing strategy of huTSLP mice. The mouse Tslp endogenous domain was replaced with the human TSLP domain. The murine signal peptide was preserved.
Figure 2. Gene editing strategy of hTSLPR mice. Part of exon 1 to intron 7 of Mouse Crlf2 was replaced with Human CRLF2 CDS-Mouse Crlf2 CDS cassette.
Figure 2. Gene editing strategy of hTSLPR mice. Part of exon 1 to intron 7 of Mouse Crlf2 was replaced with Human CRLF2 CDS-Mouse Crlf2 CDS cassette.
Application Area
Screening, development, and safety evaluation of TSLP/TSLPR-targeted drugs;
Mechanism research and development of treatment methods for allergic diseases, inflammations, and autoimmune diseases.
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