B-hTTR*V30M mice plus

C57BL/6JNifdc-Ttrtm4(TTR*V30M)Bcgen/Bcgen • 114193

B-hTTR*V30M mice plus

Product nameB-hTTR*V30M mice plus
Catalog number114193
Strain nameC57BL/6JNifdc-Ttrtm4(TTR*V30M)Bcgen/Bcgen
Strain backgroundC57BL/6JNifdc
NCBI gene ID7276 (Human)
AliasesCTS; TTN; ATTR; CTS1; PALB; TBPA; HEL111; HsT2651

이 페이지에서

  • Description
  • Targeting strategy
  • Phenotypic analysis

포스터

모두 보기

    출판물

      Description
      • Background: Transthyretin (TTR) is a tetrameric transport protein primarily synthesized in the liver, choroid plexus, and retinal pigment epithelium. It functions to transport thyroid hormone thyroxine and retinol-binding protein bound to retinol (vitamin A). Mutations in TTR are associated with inherited transthyretin amyloidosis (ATTRv), a progressive and fatal disease characterized by misfolding of TTR and aggregation as amyloid fibrils, predominantly leading to cardiomyopathy or polyneuropathy. Additionally, wild-type TTR misfolding can cause age-related transthyretin amyloid cardiomyopathy. Besides its transport role, TTR may also play a part in neuroprotection and promotion of neurite outgrowth in response to injury.
      • Targeting strategy: The exons 1-4 of mouse Ttr gene that encode whole protein domains are replaced by human counterparts containing p.V30M mutation in B-hTTR*V30M mice plus. The promoter, 5’UTR and 3’UTR regions of the mouse gene are replaced by human counterparts, and mouse Ttr gene transcription and translation will be disrupted.
      • Validation: Human prealbumin (TTR) was exclusively detectable in B-hTTR*V30M mice plus but not in wild-type mice.
      • Application: This is a disease model mouse of transthyretin amyloidotic polyneuropathy (ATTR-PN). It can be used for small nucleic acid drug screening and pharmacodynamic research, as well as for safety evaluation.
      Targeting Strategy

      Gene targeting strategy for B-hTTR*V30M mice plus. The exons 1-4 of mouse Ttr gene that encode whole protein domains are replaced by human counterparts containing p.V30M mutation in B-hTTR*V30M mice plus. The promoter, 5’UTR and 3’UTR regions of the mouse gene are replaced by human counterparts, and mouse Ttr gene transcription and translation will be disrupted.

      Protein Expression Analysis of mTTR

      Strain specific TTR expression analysis in homozygous B-hTTR*V30M mice plus by ELISA. Plasma was collected from wild-type C57BL/6JNifdc mice (+/+) (female, 8-week-old, n=3) and homozygous B-hTTR*V30M mice plus (H/H) (female, 7-week-old, n=3), and then analyzed by ELISA with species-specific Prealbumin ELISA kit (abcam, ab282297). Mouse prealbumin (TTR) was only detectable in wild-type C57BL/6JNifdc mice but not in homozygous B-hTTR*V30M mice plus.

      Protein Expression Analysis of hTTR

      Strain specific hTTR expression analysis in homozygous B-hTTR*V30M mice plus by ELISA. Plasma was collected from wild-type C57BL/6 mice (+/+) (female, 8-week-old, n=3) and homozygous B-hTTR*V30M mice plus (H/H) (female, 7-week-old, n=3; male, 7-week-old, n=3), and then analyzed by ELISA with species-specific Prealbumin ELISA kit (abcam, ab231920). Human prealbumin (TTR) was exclusively detectable in B-hTTR*V30M mice plus but not in wild-type mice.

      * When publishing results obtained using this animal model, please acknowledge the source as follows: The animal model [B-hTTR*V30M mice plus] (Cat# 114193) was purchased from Biocytogen.