B-hIL1RAcP mice

C57BL/6-Il1raptm1(IL1RAP)Bcgen/Bcgen • 110072

B-hIL1R1 mice
B-hIL2 mice

B-hIL1RAcP mice

Product nameB-hIL1RAcP mice
Catalog number110072
Strain nameC57BL/6-Il1raptm1(IL1RAP)Bcgen/Bcgen
Strain backgroundC57BL/6
NCBI gene ID16180
AliasesIL1RAP; IL1RAcP; IL1R3; C3orf13

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  • Phenotypic analysis

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      mRNA expression analysis
      Strain specific analysis of IL1RAcP gene expression in wild type and B-hIL1RAcP mice by RT-PCR. Mouse IL1RAcP mRNA was detectable in liver of wild type mice (+/+). Human IL1RAcP mRNA was detectable only in B-hIL1RAcP mice (H/H) but not in wild type mice.
      Protein expression analysis

      Strain specific IL1RAcP expression analysis in homozygous B-hIL1RAcP mice by flow cytometry. Macrophages and monocytes were collected from wild type and homozygous B-hIL1RAcP mice (H/H) and analyzed by flow cytometry with species-specific anti-IL1RAcP antibody. Human IL1RAcP were exclusively detectable in homozygous B-hIL1RAcP mice but not in wild type mice.

      Functional verification of B-hIL1RAcP mice

      Splenocytes were collected from wild-type mice and homozygous B-hIL1RAcP mice and stimulated with IL1/IL33/IL36 protein. The expression of cytokines such as IL6, TNFa, KC/GRO, IL4, IFNg, IL5, and IL12p70 in splenocytes culture medium was detected after 48 hours. The results showed that murine IL1/IL33/IL36 protein effectively activated splenocytes in wild mice and triggered the secretion of related cytokines. Murine IL1B and murine IL33 proteins could effectively activate splenocytes in B-hIL1RAcP mice and trigger the secretion of related cytokines, while murine IL36 protein could not effectively activate B-hIL1RAcP mice splenocytes.