Figure 1
Figure 1. scid mutation does not affect HSC pools. BM cells from scid, Rag1−/−, and WT mice were assayed by multiparameter FACS for proportion of HSC populations. At least 6 age-matched (8-10 weeks old) mice per genotype were compared. Representative FACS profiles of pregated on live, lineage negative cells, Sca1+, c-Kit+ (LSK) are shown in panel A, long-term HSCs (LSK, CD34−, Flk2−) and short-term HSCs (LSK, CD34−, Flk2+) are shown in panel C, and SLAM+ LSK (CD48−, CD150+,LSK) are shown in panel E. Frequencies of HSCs, LT-HSCs, ST-HSCs, and SLAM+LSK in BM from WT, scid, and Rag1−/− mice are analyzed in panels B, D, and F. Error bars indicate SD; significance was determined by a Student 2-tailed t test.

scid mutation does not affect HSC pools. BM cells from scid, Rag1−/−, and WT mice were assayed by multiparameter FACS for proportion of HSC populations. At least 6 age-matched (8-10 weeks old) mice per genotype were compared. Representative FACS profiles of pregated on live, lineage negative cells, Sca1+, c-Kit+ (LSK) are shown in panel A, long-term HSCs (LSK, CD34, Flk2) and short-term HSCs (LSK, CD34, Flk2+) are shown in panel C, and SLAM+ LSK (CD48, CD150+,LSK) are shown in panel E. Frequencies of HSCs, LT-HSCs, ST-HSCs, and SLAM+LSK in BM from WT, scid, and Rag1−/− mice are analyzed in panels B, D, and F. Error bars indicate SD; significance was determined by a Student 2-tailed t test.

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