top
Please input keywords
Order
*Country
日本
アメリカ
中国
オーストラリア
シンガポール
イギリス
フランス
ドイツ
スイス
イタリア
カナダ
韓国
オランダ
ベルギー
スウェーデン
その他
*Province
*City
*Name
*Telephone
*Company
*Position
*Email
*Verification code
*Verification Code
B-hCD10 MC38
Common name
B-hCD10 MC38 Catalog number    321959
Aliases NEP; SFE; CD10; CALLA; CMT2T; SCA43 Disease  Colon carcinoma
Organism
Mouse 
Strain  C57BL/6
Tissue types Colon Tissue  Colon
Description 

The mouse CD10 gene was replaced by human CD10 coding sequence in B-hCD10 MC38 cells. Human CD10 is highly expressed on the surface of B-hCD10 MC38 cells.

Application

B-hCD10 MC38 cells have the capability to establish tumors in vivo and can be used for efficacy studies.

Targeting strategy

Gene targeting strategy for B-hCD10 MC38 cells. The exogenous promoter and human CD10 coding sequence was inserted to replace part of murine exon 2-3. The insertion disrupts the endogenous murine CD10 gene, resulting in a non-functional transcript.

Protein expression analysis 

from clipboard

CD10 expression analysis in B-hCD10 MC38 cells by flow cytometry. Single cell suspensions from wild-type MC38 and B-hCD10 MC38 cultures were stained with species-specific anti-CD10 antibody. Human CD10 was detected on the surface of B-hCD10 MC38 cells but not wild-type MC38 cells. The 1-G07 clone of B-hCD10 MC38 cells was used for in vivo experiments.

Tumor growth curve & Body weight changes

from clipboard

Subcutaneous homograft tumor growth of B-hCD10 MC38 cells. B-hCD10 MC38 cells (5x106) and wild-type MC38 cells (5x105) were subcutaneously implanted into C57BL/6 mice (female, 11-12-week-old, n=6). Tumor volume and body weight were measured twice a week. (A) Average tumor volume ± SEM. (B)  Body weight (Mean± SEM). Volume was expressed in mm3 using the formula: V=0.5 X long diameter X short diameter2. As shown in panel A, B-hCD10 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.

Tumor growth curve of individual mice

from clipboard

B-hCD10 MC38 tumor cells growth of individual mice. B-hCD10 MC38 cells (5x106) and wild-type MC38 cells (5x105) were subcutaneously implanted into C57BL/6 mice (female, 11-12-week-old, n=6). As shown in panel, B-hCD10 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.

Protein expression analysis of tumor cells

from clipboard

B-hCD10 MC38 cells were subcutaneously transplanted into C57BL/6 mice (n=6), and on 28 days post inoculation, tumor cells were harvested and assessed for human CD10 expression by flow cytometry. As shown, human CD10 was highly expressed on the surface of tumor cells. Therefore, B-hCD10 MC38 cells can be used for in vivo efficacy studies of novel CD10 therapeutics.