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We performed three additional experiments using CD2715 M" M2 K7 x; G
for enrichment of MSC. Upon isolation of MNC by Ficoll2 g6 i" s8 @: D9 {7 W
density fractionation, half of the sample was processed
( u% E* `# L9 n: h( Z1 i6 Zfurther using the CD271 MicroBead Kit. About 5% of the cells were in the positive fraction and about 50% of these4 z9 ]6 v+ }% ]& Z; s6 }& g
were CD271, as determined by flow cytometry. CFU-F4 B+ l) w5 ?% _+ d1 y; ]
were exclusively found in the CD271 fraction, as- f/ R6 E0 \7 w, |+ s# u6 S
described elsewhere [22]. The number of CFU-F per" F9 ]. S9 j+ ?- T2 X: k4 K
cell was 210 times higher in CD271 cells in comparison
' k( E4 T2 o2 b+ H5 {1 g( `with MNC. Hence MSC were enriched in the CD271/ C+ V1 f" t: h! H- l
fraction, although the yield of CFU-F per milliliter BM
# [) f+ n- k7 R$ c0 `5 Kaspirate or with regard to the number of MNC was greatly
. Z; f% B% h! \0 S0 Sreduced. |
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