XIE/2:2025/Dec: Difference between revisions

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#Group 1: add S1, S2, and TFO , 2 µL each.
#Group 1: add S1, S2, and TFO , 2 µL each.
#Group 2: add S-S1, S-S2, and S-TFO , 2 µL each.
#Group 2: add S-S1, S-S2, and S-TFO , 2 µL each.
{| class="wikitable"style="width:80%;"
 
! Name
! Buffer
! SsDNA
|-
| 5.5-1
| 194 uL, pH 5.5
| S1, S2, TFO 各 2 uL
|-
| 5.5-2
| 149 uL, pH 5.5
| S‑S1, S‑S2, S‑TFO 各 2 uL
|-
| 6.5-1
| 194 uL, pH 6.5
| S1, S2, TFO 各 2 uL
|-
| 6.5-2
| 194 uL, pH 6.5
| S‑S1, S‑S2, S‑TFO 各 2 uL
|-
| 7.0-1
| 194 uL, pH 7.0
| S1, S2, TFO 各 2 uL
|-
| 7.0-2
| 194 uL, pH 7.0
| S‑S1, S‑S2, S‑TFO 各 2 uL
|-
| 7.5-1
| 194 uL, pH 7.5
| S1, S2, TFO 各 2 uL
|-
| 7.5-2
| 194 uL, pH 7.5
| S‑S1, S‑S2, S‑TFO 各 2 uL
|-
| 8.5-1
| 194 uL, pH 8.5
| S1, S2, TFO 各 2 uL
|-
| 8.5-2
| 194 uL, pH 8.5
| S‑S1, S‑S2, S‑TFO 各 2 uL
|}
*PCR: 37℃ 3h
*PCR: 37℃ 3h



Revision as of 08:52, 13 December 2025

12.12

  • Triplex DNA pH Test

Sample preparation

  • ssDNA stocks: s1 (3'Cy5), S2, TFO (3'Cy3), S‑S1 (3'Cy5), S‑S2, and S‑TFO (3'Cy3) were each prepared at 1 mM in nuclease-free water.
  • Buffers: PBS adjusted to pH 5.5, 6.5, 7.0, 7.5, and 8.5; prepare 50 mL of each pH condition.

Incubation

  • For each pH condition, set up two groups (Group 1 and Group 2). To each reaction, first add 194 µL of the corresponding PBS buffer.
  1. Group 1: add S1, S2, and TFO , 2 µL each.
  2. Group 2: add S-S1, S-S2, and S-TFO , 2 µL each.
  • PCR: 37℃ 3h

荧光分光光度计

  • 样品处理:每个样稀释至1%
  • 测量通道
  1. IDA-measure:激发波长 550 nm;发射波长 670 nm
  2. IDD-measure:激发波长 550 nm;发射波长 570 nm
  3. IAA-measure:激发波长 650 nm;发射波长 670 nm