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Sftpc-MerCreMer Mouse
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Sftpc-MerCreMer Mouse
제품명
Sftpc-MerCreMer Mouse
제품 ID
C001501
품종 계통
C57BL/6JCya-Sftpcem2(IRES-MerCreMer)/Cya
Backgroud
C57BL/6JCya
상태
이 마우스 계통을 논문에서 사용할 경우, “Sftpc-MerCreMer Mouse (카탈로그 번호 C001501)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
Inducible Cre Mouse Models
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
가격 문의
Inducible Cre Mouse Models
기본 정보
검증 데이터
관련 자료
기본 정보
유전자명
유전자 별칭
SP5, SPC, SP-C, Sftp2, Bricd6, Sftp-2, pro-SpC
NCBI ID
염색체
Chr 14
MGI ID
Datasheet
품종 계통 설명
The SFTPC gene encodes surfactant protein C (SP-C), one of the four key proteins in surfactant. Surfactant is a mixture of lipids and proteins that coats the lung tissue, making breathing easier. Surfactant is secreted by alveolar cells and maintains the stability of the lung tissue by reducing the surface tension of the fluid that covers the lung. In addition, SP-C is involved in lung development and function, including alveolar septation, airway remodeling, and immune defense. The SFTPC gene is primarily expressed in the lung, with the highest expression in the lower lobe, right lung, upper lobe, left upper lobe, and visceral pleura. It is also expressed at low levels in other tissues. Type II alveolar cells are responsible for the production and secretion of surfactants. Therefore, the SFTPC gene is primarily expressed in these cells and can be used as a specific marker for these cells.
Sftpc-MerCreMer mice were generated to integrate the tamoxifen-inducible MerCreMer recombinase expression element into the 3’UTR of the mouse Sftpc gene. This mimics the expression pattern of the endogenous gene while maintaining Sftpc expression. When bred with mice carrying a loxP site-flanked sequence, Cre recombinase-mediated recombination of the flanked sequence occurs in type II alveolar cells, following tamoxifen induction.
변형 전략
The IRES-MerCreMer gene expression element was integrated into the 3'UTR of the mouse Sftpc gene.

Figure 1. Diagram of the gene editing strategy for the generation of Sftpc-MerCreMer mice.
검증 데이터
1. Method
Sftpc-MerCreMer mice were mated with Rosa26-LSL-tdTomato mice to generate double heterozygous zygote mice. Tamoxifen induction (4 mg/mouse for 4 days, i.p.) was performed at 6 weeks of age, resulting in Cre recombinase-mediated deletion of the LSL elements and subsequent expression of tdTomato in Cre-positive cells. One week after induction, Lung, trachea, and kidney tissue was collected from the offspring, and the distribution of tdTomato was determined by Immunofluorescent staining to assess Cre recombinase expression. The control group received the same dose of corn oil.
2. Groups
Cre+Tam+: Sftpc-MerCreMer[KI/+];Rosa26-LSL-tdTomato[CKI/+], Tamoxifen-induced;
Cre+Tam-: Sftpc-MerCreMer[KI/+];Rosa26-LSL-tdTomato[CKI/+], Corn oil-treated;
3. Result
(1)Expression of Cre recombinase in the lung
Results showed that strong Cre recombinase activity was present in type II alveolar cells of mice induced by tamoxifen (Cre+Tam+). Cre recombinase activity was not detected in the lungs of mice in the non-Tamoxifen-induced group (Cre+Tam-). These results suggest that Cre recombinase activity and specificity in the mouse lung tissue are high, and there is no expression leakage.

Figure 2. Immunofluorescence (IF) staining of lung tissues.
(2)Expression of Cre recombinase in other tissues
Immunofluorescent staining was performed to detect the expression of tdTomato protein in the trachea and kidney tissue of mice. Results showed that Cre recombinase activity was present in a subset of tracheal cells of mice induced by tamoxifen (Cre+Tam+), but not in the kidney. Cre recombinase activity was not detected in these areas of mice in the non-Tamoxifen-induced group (Cre+Tam-). These results suggest that a small amount of Cre recombinase activity is present in a subset of the tracheal tissue of mice.

Figure 3. Immunofluorescence (IF) staining of trachea and kidney tissue.
4. Summary
In the Sftpc-MerCreMer mouse model, Cre recombinase is predominantly expressed in type II alveolar cells. Overall, the mice do not exhibit pre-induction expression leakage. In conclusion, this model is a highly tissue-specific Cre mouse targeting type II alveolar cells.
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