녹아웃(KO) 마우스 | Cyagen Korea
  1. Home
  2. 커뮤니티
  3. 프로모션
  4. COVID-19 연구에 도움이 되는 ACE2 마우스 모델 검증 데이터
COVID-19 연구에 도움이 되는 ACE2 마우스 모델 검증 데이터
COVID-19의 대유행은 전세계적으로 큰 피해를 주고 있습니다. 이와 동시에 전 세계의 많은 과학 연구팀이 시간과의 싸움에서 백신을 개발하고 있습니다. 동물 실험은 백신 개발의 필수 단계로 동물 실험을 거친 백신만 임상시험에 들어갈 수 있습니다. 이전에는 각국의 연구팀이 촌각을 다투어 백신 개발에 나섰으며 코로나19 백신 실험용 마우스 모델도 공급부족으로 한 마리도 구하기 힘든 상황이였습니다. Cyagen에서 자체 개발한 TurboKnockout 기술과 최적화된 CRISPR-Pro 기술을 활용하여 BALB/c, C57BL/6J, C57BL/6N 세 가지 strain의 ACE2 마우스를 제작하였으며 다양한 유전자 편집 방법의 장단점을 고려하여 여러가지 제작 전략을 설계함으로써 연구자의 다양한 연구 목적과 여러 응용 방향에 대한 요구를 충족시켰습니다. 아울러 Cyagen에서는 코로나19 관련 연구에 전념하는 연구자들을 위해 ACE2 마우스 모델에 대한 검증 데이터 보고서를 제공합니다. 코로나19 연구 관련 마우스 모델 필요하신 경우 +86 20-31601779 또는 [email protected]으로 연락 부탁드립니다.
ACE2 마우스 모델 추천
Project Type Background Strain Order
ACE2 Humanized Model C57BL/6J
C57BL/6N
BALB/c
ACE2 Knock-In Model (H11 Locus) C57BL/6J
ACE2 Conditional Knock-In Model (Rosa26 Locus) C57BL/6J
BALB/c
C57BL/6N
ACE2 Knock-Out (KO) Model C57BL/6J
BALB/c
ACE2 마우스 모델 검증 데이터 보고서
1. C57BL/6J ACE2 Humanized Mice
● qPCR Validation:
The results:
a. Model Generation:
Model Name: ACE2-KI; Strain Background: C57BL/6J
Construction Strategy: Retain the mouse signal peptide and endogenous PolyA; replace the extracellular domain, transmembrane domain, and intracellular domain of mouse with that of human.
b. After the model was established, different tissues of the mice were taken for qPCR verification. The results show ACE2 was expressed in the small and large intestine, kidney, lung, and trachea, which means that the humanized model can successfully express human ACE2 protein, and the model verification is successful.
2. C57BL/6J ACE2 Humanized Mice
● IHC-P Validation:
The results:
a. Model Generation:
Model Name: ACE2-KI; Strain Background: C57BL/6J
Construction Strategy: retain the mouse signal peptide and endogenous PolyA; replace the extracellular domain, transmembrane domain, and intracellular domain of mouse with that of human.
b. After the model was established, different tissues of the mice were fixed in formaldehyde, embedded in paraffin, and immunohistochemical experiments were performed. The results showed ACE2 was expressed in the intestines, kidneys, lungs, and trachea - which further confirmed that the humanized model can successfully express human ACE2 protein, and the model verification is successful.
● C57BL/6J Negative Control:
The results:
a. Mouse Model: C57BL/6J background, negative control.
b. Tissues of C57BL/6J blank control mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The result reported negative in the intestines, lungs, liver, brain, trachea, kidney, stomach, and heart.
3. C57BL/6J ACE2 Humanized Mice
● WB Verification - Expression variations across organs:
The results:
The six tissues of mice including the large intestine, small intestine, kidney, brain, trachea, and lung were tested separately; the theoretical band size of ACE2 is 92KD - the protein may be too large due to glycosylation modification in the protein.
Conclusions:
1. In the brain and lung tissues, all target clones have no detectable bands that are significantly different from the wild type;
2. In kidney tissue, the theoretical band size is 92KD, while the actual band size is 120KD.
3. In the large intestine tissue, the theoretical band size is 92KD, while the actual band size is 130KD.
4. In tracheal tissue, theoretical band size is 92KD, while the actual band size is 120KD.
5. In the small intestine tissue, the theoretical band size is 92KD, while the actual band size is 130KD.
The expression of ACE2 in humanized ACE2 mice varies greatly among individuals and different tissues.
1. BALB/c ACE2 Humanized Mice
● IHC-P Validation:
The results:
a. Model Generation:
Model Name: ACE2-KI; Strain Background: BALB/c
Construction Strategy: Retain the mouse signal peptide and endogenous PolyA, replace the extracellular domain, transmembrane domain,and intracellular domain of mouse with that of human.
b. After the model was established, different tissues of the mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The results showed ACE2 was expressed in the intestines, lungs, liver, brain, trachea, kidney, stomach, and heart - which further confirmed that the humanized model can successfully express human ACE2 protein, and the model verification is successful.
● BALB/c Negative Control:
The results:
a. Mouse Model: BALB/c background, negative control.
b. Tissues of BALB/c blank control mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The result reported negative in the intestines, lungs, liver, brain, trachea, kidney, stomach, and heart.
1. C57BL/6J ACE2 Knockin Mouse (H11 Locus)
● IHC-P Validation:
The results:
a. Model Generation:
Model Name: H11-ACE2-KI; Strain Background: C57BL/6J
Construction Strategy: The human signal peptide, extracellular domain, transmembrane domain, and intracellular domain were inserted into the mouse H11 locus.
b. After the model was established, different tissues of the mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The results showed different levels of ACE2 expression in the intestine, lung, liver, brain, trachea, kidney, stomach, and heart, while K18 promoter still has nonspecific expression, which can be selected according to different experimental needs.
● C57BL/6J Negative Control:
The results:
a. Mouse Model: C57BL/6J background, negative control.
b. Tissues of C57BL/6J blank control mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The result reported negative in the intestines, lungs, liver, brain, trachea, kidney, stomach, and heart.
1. C57BL/6J ACE2 Knockout Mice
● IHC-P Validation:
The results:
a. Model Generation:
Model Name: ACE2-KO
Strain Background: C57BL/6J
b. After the model was established, different tissues of the mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The negative results reported in the intestines, lungs, liver, brain, trachea, kidney, stomach, and heart confirmed that no measurable ACE2 expression occurred in knockout (KO) mice – indicating successful KO model generation.
● C57BL/6J Negative Control:
The results:
a. Mouse Model: C57BL/6J background, negative control.
b. Tissues of C57BL/6J blank control mice were fixed in formaldehyde, embedded in paraffin, and evaluated by immunohistochemical experiments. The result reported negative in the intestines, lungs, liver, brain, trachea, kidney, stomach, and heart.
Cyagen Coronavirus Research News & Updates