B-h4-1BB/hTNFR2 mice plus

C57BL/6-Tnfrsf9tm1(TNFRSF9)BcgenTnfr2tm2(TNFR2)Bcgen/Bcgen • 111958

B-h4-1BB/hTIGIT mice
B-hA2AR mice

B-h4-1BB/hTNFR2 mice plus

Product nameB-h4-1BB/hTNFR2 mice plus
Catalog number111958
Strain nameC57BL/6-Tnfrsf9tm1(TNFRSF9)BcgenTnfr2tm2(TNFR2)Bcgen/Bcgen
Strain backgroundC57BL/6
NCBI gene ID3604,7133 (Human)
Aliases4-1BB, CD137, CDw137, ILA; CD120b, TBPII, TNF-R-II, TNF-R75, TNFBR, TNFR1B, TNFR2, TNFR80, p75, p75TNFR

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  • Phenotypic analysis
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    发表文章

      Protein expression analysis
      Strain specific TNFR2 expression analysis in heterozygous B-h4-1BB/hTNFR2 mice plus by flow cytometry. Splenocytes were collected from wild-type mice (+/+) and heterozygous B-h4-1BB/hTNFR2 mice plus (H/+) stimulated with anti-CD3ε in vivo (7.5 μg/mice, 24 hours, i.p.), and analyzed by flow cytometry with species-specific anti-TNFR2 antibody. Mouse TNFR2 was detectable in wild-type mice and heterozygous B-h4-1BB/hTNFR2 mice plus, but human TNFR2 was only detectable in heterozygous B-h4-1BB/hTNFR2 mice plus.
      Strain specific TNFR2 expression analysis in heterozygous B-h4-1BB/hTNFR2 mice plus by flow cytometry. Splenocytes were collected from wild-type mice (+/+) and heterozygous B-h4-1BB/hTNFR2 mice plus (H/+) stimulated with anti-CD3ε in vivo (7.5 μg/mice, 24 hours, i.p.), and analyzed by flow cytometry with species-specific anti-TNFR2 antibody. Mouse TNFR2 was detectable in wild-type mice and heterozygous B-h4-1BB/hTNFR2 mice plus, but human TNFR2 was only detectable in heterozygous B-h4-1BB/hTNFR2 mice plus.
      Strain specific TNFR2 expression analysis in heterozygous B-h4-1BB/hTNFR2 mice plus by flow cytometry. Splenocytes were collected from wild-type mice (+/+) and heterozygous B-h4-1BB/hTNFR2 mice plus (H/+) stimulated with anti-CD3ε in vivo (7.5 μg/mice, 24 hours, i.p.), and analyzed by flow cytometry with species-specific anti-TNFR2 antibody. Mouse TNFR2 was detectable in wild-type mice and heterozygous B-h4-1BB/hTNFR2 mice plus, but human TNFR2 was only detectable in heterozygous B-h4-1BB/hTNFR2 mice plus.
      Strain specific 4-1BB expression analysis in heterozygous B-h4-1BB/hTNFR2 mice plus by flow cytometry. Splenocytes were collected from wild-type mice (+/+) and heterozygous B-h4-1BB/hTNFR2 mice plus (H/+) stimulated with anti-CD3ε in vivo (7.5 μg/mice, 24 hours, i.p.), and analyzed by flow cytometry with species-specific anti-4-1BB antibody. Mouse 4-1BB was detectable in wild-type mice and heterozygous B-h4-1BB/hTNFR2 mice plus, but human 4-1BB was only detectable in heterozygous B-h4-1BB/hTNFR2 mice plus.
      Strain specific 4-1BB expression analysis in heterozygous B-h4-1BB/hTNFR2 mice plus by flow cytometry. Splenocytes were collected from wild-type mice (+/+) and heterozygous B-h4-1BB/hTNFR2 mice plus (H/+) stimulated with anti-CD3ε in vivo (7.5 μg/mice, 24 hours, i.p.), and analyzed by flow cytometry with species-specific anti-4-1BB antibody. Mouse 4-1BB was detectable in wild-type mice and heterozygous B-h4-1BB/hTNFR2 mice plus, but human 4-1BB was only detectable in heterozygous B-h4-1BB/hTNFR2 mice plus.
      Strain specific 4-1BB expression analysis in heterozygous B-h4-1BB/hTNFR2 mice plus by flow cytometry. Splenocytes were collected from wild-type mice (+/+) and heterozygous B-h4-1BB/hTNFR2 mice plus (H/+) stimulated with anti-CD3ε in vivo (7.5 μg/mice, 24 hours, i.p.), and analyzed by flow cytometry with species-specific anti-4-1BB antibody. Mouse 4-1BB was detectable in wild-type mice and heterozygous B-h4-1BB/hTNFR2 mice plus, but human 4-1BB was only detectable in heterozygous B-h4-1BB/hTNFR2 mice plus.
      Tumor growth curve & Body weight changes

      Subcutaneous homograft tumor growth of MC38 cells in homozygous B-h4-1BB/hTNFR2 mice plus. Wild-type MC38 cells (5x105) were subcutaneously implanted into B-h4-1BB/hTNFR2 mice plus (female, 8-week-old, n=6). Tumor volume and body weight were measured twice a week. (A) Average tumor volume ± SEM. (B) Body weight (Mean± SEM). (C) Tumor growth curve of individual mice. Volume was expressed in mm3 using the formula: V=0.5 X long diameter X short diameter2. As shown in panel A, MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.