||B-hPD-L1 LLC1||Catalog number||
|Aliases||CD274, PDCD1L1||Disease||Lewis lung carcinoma|
The mouse Pdl1 gene was replaced by human PD-L1 coding sequence in B-hPD-L1 LLC1 cells. Human PD-L1 is highly expressed on the surface of B-hPD-L1 LLC1 cells.
B-hPD-L1 LLC1 cells have the capability to establish tumors in vivo and can be used for efficacy studies.
The exogenous promoter and human PD-L1 coding sequence was inserted to replace part of murine exon 3. The insertion disrupts the endogenous murine Pdl1 gene, resulting in a non-functional transcript.
Protein expression analysis
PD-L1 expression analysis in B-hPD-L1 LLC1 cells by flow cytometry. Single cell suspensions from wild-type LLC1 and B-hPD-L1 LLC1 cultures were stained with species-specific anti-PD-L1 antibody. Mouse PD-L1 was detected on the surface of wild-type LLC1 cells. Human PD-L1 was detected on the surface of B-hPD-L1 LLC1 cells but not wild-type LLC1 cells. The 1-A5 clone of B-hPD-L1 LLC1 cells was used for in vivo experiments.
Tumor growth curve & Body weight changes
Subcutaneous homograft tumor growth of B-hPD-L1 LLC1 cells. B-hPD-L1 LLC1 cells (2x105) were subcutaneously implanted into C57BL/6 mice (female, 5-6-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-hPD-L1 LLC1 cells were able to establish tumors in vivo and can be used for efficacy studies.