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Primers for mir 21 and u6

Manufactured by RiboBio
Sourced in China

Primers for miR-21 and U6 are oligonucleotide sequences designed for the detection and quantification of specific RNA molecules, miR-21 and U6, using various molecular biology techniques such as Real-Time PCR and Northern Blotting. These primers provide a tool for researchers to study the expression patterns and functions of these RNA targets.

Automatically generated - may contain errors

2 protocols using primers for mir 21 and u6

1

Quantifying Gingival MSC Gene Expression

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Total RNA was isolated from Gingival MSCs using Trizol reagents (Invitrogen, USA) and reverse transcribed into cDNA using PrimeScriptRT reagent Kit with gDNA Eraser (Takara, Dalian, China). The real-time PCR reactions were performed using the SYBR Premix Ex Taq II (Takara, Dalian, China) and IcycleriQ Multi-color Real-time PCR Detection System. The primers were synthesized by Sangon Biotech: Sp1 (5′-TGAGACAGCAGGTGGAGAAG-3′, 5′-GGCTCTTCCCTCACTGTCTT-3′); tert (5′-TGCTGGACACTCAGACTTTGGA-3′, 5′-TTCAACCGCAAGACCGACA-3′); GAPDH (5′-TGAAGCAGGCATCTGAGGG-3′, 5′-CGAAGGTGGAAGAGTGGGAG-3′). Primers for miR-21 and U6 are purchased from RiboBio (Guangzhou, China).
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2

Quantifying Exosomal miRNA Expression

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Total RNA was isolated from the exosomal pellets, the exosome-depleted supernatant, and whole serum using isothiocyanate-phenol/chloroform extraction procedures. miR-21 expression was examined as previously described [13 ]. Real-time quantitative RT-PCR (qRT-PCR) was performed using SYBR Premix DimerEraser kit (TaKaRa, Shiga, Japan) on an ABI Prism 7900HT Detection System (Applied Biosystems, Foster City, CA). U6 snRNA was used as an internal control. The primers for miR-21 and U6 were purchased from RiboBio (Guangzhou, China).
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