B-hC3 mice

C57BL/6N-C3tm2(C3)Bcgen/Bcgen • 112467

B-hC1S mice
B-hC5 mice

B-hC3 mice

Product nameB-hC3 mice
Catalog number112467
Strain nameC57BL/6N-C3tm2(C3)Bcgen/Bcgen
Strain backgroundC57BL/6N
AliasesASP; C3a; C3b; AHUS5; ARMD9; CPAMD1; HEL-S-62p

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  • Phenotypic analysis
  • Physiological data

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      Protein expression analysis in serum

      Strain specific C3 expression analysis in homozygous B-hC3 mice by ELISA. Serum were collected from wild-type mice (+/+) and homozygous B-hC3 mice (H/H), and analyzed by ELISA with species-specific anti-C3 antibody. Mouse C3 was detectable in wild-type mice. Human C3 was detectable in homozygous B-hC3 mice.

      train specific C3 expression analysis in homozygous B-hC3 mice by ELISA. Serum were collected from 10, 12 and 14-week-old homozygous B-hC3 mice (H/H), and analyzed by ELISA with anti-C3 ELISA kit. Human C3 was detectable in homozygous B-hC3 mice. The expression of human C3 did not change significantly with the increase of age. (*p<0.05,***p<0.001, ****p<0.0001)

      Analysis of blood biochemistry in B-hC3 mice
      Analysis of blood biochemical in hC3 and WT. Serum were collected from wild-type mice (+/+) and homozygous B-hC3 mice (H/H), and analyzed for biochemistry. Biochemistry analysis revealed that the B-hC3 mice presented with significant elevation of BUN and sCysC(10w and 14w). The B-hC3 mice also showed significant elevation of liver injury markers, such as alanine aminotransferase(ALT), aspartate aminotransferase(AST), and alkaline Phosphatase(ALP).(*p
      The expression of hC5b-9 in kidney of 12-week-old B-hC3 mice by IF

      Staining of C5b-9MAC in hC3 and WT mice. The C5b-9 MAC were stained in the kidneys of both the WT mice(C) and B-hC3 mice(D). These results were not consistent with the data in the literature. In theory, the kidneys of wild-type mice have very few deposits of the C5b-9 MAC.

      Kidney, liver and brain lesions of 26-week-old B-hC3 mice

      Histopathology of the livers, kidneys and brains from the hC3 and WT mice. Compared with the WT mice, no significant lesions were observed in the kidney, liver or brain from the hC3 mice.