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Taqman one step pcr master mix reagents kit

Manufactured by Thermo Fisher Scientific

The TaqMan One Step PCR Master Mix Reagents Kit is a ready-to-use solution for performing one-step reverse transcription and quantitative PCR (RT-qPCR) reactions. The kit includes all the necessary components, including a proprietary enzyme blend, buffers, and dNTPs, to facilitate the detection and quantification of RNA targets.

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2 protocols using taqman one step pcr master mix reagents kit

1

qRT-PCR Analysis of HPSE and p53 Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
For the qRT-PCR, 100 ng of total RNA was used to prepare cDNA (TaqMan One Step PCR Master Mix Reagents Kit) (Applied Biosystem, Carlsbad, CA). Specific primers and probes that were designed, tested, and standardized by Applied Biosystems for HPSE and p53 were used (HPSE: Hs00935036_m1; p53: Hs01034249_m1). The difference in cycle threshold values (ΔCT) of HPSE was normalized to the ΔCT of GAPDH (Glyceraldehude-3-phospate dehydrogenase, Hs99999905_m1), and the fold-change in expression was expressed relative to CD14+ monocytes, considered as a positive control while mesemchymal stem cells were used as a negative control. For p53 mRNA quantification the difference in cycle threshold values (ΔCT) of p53 was normalized to the ΔCT of GAPDH (Glyceraldehyde-3-phospate dehydrogenase, Hs99999905_m1), and the fold-change in expression was expressed relative to FI-T.
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2

qRT-PCR Analysis of HPSE and p53 Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
For the qRT-PCR, 100 ng of total RNA was used to prepare cDNA (TaqMan One Step PCR Master Mix Reagents Kit) (Applied Biosystem, Carlsbad, CA). Specific primers and probes that were designed, tested, and standardized by Applied Biosystems for HPSE and p53 were used (HPSE: Hs00935036_m1; p53: Hs01034249_m1). The difference in cycle threshold values (ΔCT) of HPSE was normalized to the ΔCT of GAPDH (Glyceraldehude-3-phospate dehydrogenase, Hs99999905_m1), and the fold-change in expression was expressed relative to CD14+ monocytes, considered as a positive control while mesemchymal stem cells were used as a negative control. For p53 mRNA quantification the difference in cycle threshold values (ΔCT) of p53 was normalized to the ΔCT of GAPDH (Glyceraldehyde-3-phospate dehydrogenase, Hs99999905_m1), and the fold-change in expression was expressed relative to FI-T.
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