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-hCD38-Luc E.G7-OVA
Common name
B-hCD38-Luc E.G7-OVA Catalog number    311445
Aliases ADPRC 1, ADPRC1 Disease  Lymphoma
Organism
Mouse Strain  C57BL/6
Tissue types T lymphocyte Tissue  Lymphoma

Description


The mouse Cd38 gene was replaced by chimera CDS composed of human CD38 extracellular coding sequence plus mouse Cd38 cytoplasmic sequence and the full coding sequence of luciferase in B-hCD38-Luc E.G7-OVA cells. Human CD38 is highly expressed on the surface of B-hCD38-Luc E.G7-OVA cells.


Application


B-hCD38-Luc E.G7-OVA cells have the capability to establish tumors in vivo and can be used for efficacy studies.


Targeting strategy


Gene targeting strategy for B-hCD38-Luc E.G7-OVA cells. The mouse Cd38 gene was replaced by chimera CDS composed of human CD38 extracellular coding sequence plus mouse Cd38 cytoplasmic sequence and the full coding sequence of luciferase in B-hCD38-Luc E.G7-OVA cells. The replacement sequences disrupts the endogenous murine Cd38 gene, resulting in a non-functional transcript.


Protein expression analysis

from clipboard

CD38 expression analysis in B-hCD38-Luc E.G7-OVA cells by flow cytometry. Single cell suspensions from B-hCD38-Luc E.G7-OVA cultures were stained with species-specific anti-hCD38 antibody. Human CD38 was detected on the surface of B-hCD38-Luc E.G7-OVA cells. The 1-B07 clones of B-hCD38-Luc E.G7-OVA cells can be used in vivo experiments.


Luciferase reporter activity assay

from clipboard

Luciferase reporter activity assay of B-hCD38-Luc E.G7-OVA cells. Single cell suspensions from B-hCD38-Luc E.G7-OVA cultures were collected. The luciferase activities were measured by Bright-GloTM luciferase Assay System (Promega, Cat E2610), and B-hCD38-Luc E.G7-OVA cells have strong luminescence signal. The 1-B07 clones of B-hCD38-Luc E.G7-OVA cells can be used in vivo experiments.


Tumor growth curve & Body weight changes

from clipboard

Subcutaneous homograft tumor growth of B-hCD38-Luc E.G7-OVA cells. B-hCD38-Luc E.G7-OVA cells (1x105) and wild-type E.G7-OVA  cells (1x105) were subcutaneously implanted into C57BL/6 mice (female, 7-week-old, n=5). 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-hCD38-Luc E.G7-OVA cells were able to establish tumors in vivo and can be used for efficacy studies.


Protein expression analysis of tumor cells

from clipboard

B-hCD38-Luc E.G7-OVA cells were subcutaneously transplanted into C57BL/6 mice (n=5), and on 18 days post inoculation, tumor cells were harvested and assessed for human CD38 expression by flow cytometry. As shown, human CD38 was highly expressed on the surface of tumor cells. Therefore, B-hCD38-Luc E.G7-OVA cells can be used for in vivo efficacy studies of novel CD38 therapeutics.


Tumor growth curve & Body weight changes

from clipboard

Tumor growth and in vivo imaging of B-hCD38-luc E.G7-OVA. B-hCD38-Luc E.G7-OVA cells (1x105) were  injected by tail vein into C57BL/6 mice. Signal intensity and body weight were measured twice a week. (A) Imaging was performed on days 2, 6, 9, 13, 16, 20, 23 and 27, (B) Mice body weight (Mean ± SEM). B-hCD38-Luc E.G7-OVA cells can be used for in vivo efficacy evaluation.


Imaging analysis in vivo

from clipboard

In vivo luciferase images of B-hCD38-Luc E.G7-OVA cells