Figure 1.
Figure 1. Determination of the sensitivity of the TCR Vβ spectratyping technique. Detection of spectratyping sensitivity was performed on the basis of flow cytometry, and the sorted positive cells were mixed with negative cells to produce fixed proportions of the specific Vβ's in negative cell populations (0, 10, 102,103,104, and 105 Vβ+ cells in 106 cell population for each Vβ subfamily). Total RNA (aapproximately 1 μg) was extracted from cells (106), and standard spectratyping performed. The experiments were repeated 3 times. The lowest cell number detectable in 106 mixed population is 100 to 1000 cells for random selection of Vβ2, Vβ14, and Vβ22.

Determination of the sensitivity of the TCR Vβ spectratyping technique. Detection of spectratyping sensitivity was performed on the basis of flow cytometry, and the sorted positive cells were mixed with negative cells to produce fixed proportions of the specific Vβ's in negative cell populations (0, 10, 102,103,104, and 105 Vβ+ cells in 106 cell population for each Vβ subfamily). Total RNA (aapproximately 1 μg) was extracted from cells (106), and standard spectratyping performed. The experiments were repeated 3 times. The lowest cell number detectable in 106 mixed population is 100 to 1000 cells for random selection of Vβ2, Vβ14, and Vβ22.

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