1 n, magnesium sulfate, manganese sulfate, and horse serum.

2 ed in growth medium containing calf serum or horse serum.

3 awley) were cultured in MEM enriched with 5% horse serum.

4 enzoic acid, L-cysteine and L-glutamine, and horse serum.

5 ally sterilized brain-heart infusion with 2% horse serum.

6 s substrate is preconditioned by exposure to horse serum.

7  Among the conditions studied, growth in 40% horse serum (a biological cue with potential clinical re

8 ous solutions and in complex samples such as horse serum and cell culture media.

9  mucin to brain heart infusion broth with 7% horse serum (BHI-HS) enhanced the growth of H. pylori.

10  We have previously shown by proton NMR that horse serum butyryl cholinesterase, like serine protease

11 ocytes acutely isolated and then cultured in horse serum-containing medium for over 24 h.

12                                              Horse serum (HS) or bovine serum albumin (BSA) had no im

13 t by OG1RF when they were grown in TSBG plus horse serum (HS) or TSBG plus FN, and the increase was c

14 f the growth medium of cells grown either on horse serum or calf serum with free queuine had no effec

15  media supplemented with fetal bovine serum, horse serum, PIXY321, flt-3 ligand, and erythropoietin.

16 demonstrated by quantification of bromide in horse serum samples.

17                     In a DMEM medium with 6% horse serum, the TSR was increased by 19% after a pressu

18      We confirmed that the cells cultured in horse serum were devoid of Q by purifying tRNAs and asse

19 liquid media without supplementation with 5% horse serum, whereas the other two species grew poorly w

20                                    Growth in horse serum, which contains no free queuine, eliminates