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Bulge loop mir rt qpcr starter kit

Manufactured by RiboBio

The Bulge-Loop miR RT-qPCR Starter kit is a laboratory equipment product designed for the detection and quantification of microRNA (miRNA) expression levels. The kit includes reagents and protocols for reverse transcription (RT) and quantitative real-time PCR (qPCR) analysis of miRNA targets.

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3 protocols using bulge loop mir rt qpcr starter kit

1

Quantifying circVPS33B, VPS33B, and HNRNPK

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RNA Simple Total Kit (TIANGEN, Beijing, China) was utilized for total RNA separation (tissue samples and cells). The complementary DNA was synthesized with the M-MLV First Strand Kit (Life Technologies) or Bulge-Loop miR RT-qPCR Starter kit (RiboBio), followed by performing qPCR with the SYBR Green (Solarbio). Primer sequences used in the study were as follows: circVPS33B (Forward: 5ʹ-GTGGTGTTCTTGGGTGGTTGT-3ʹ; Reverse: 5ʹ-CCGCTCTAGCACCTTTCTCTC-3ʹ), VPS33B (Forward: 5ʹ-ATGAGCCCTTTGGATCGAATTG-3ʹ; Reverse: 5ʹ-ATGCGGGGTCTGACCAAGA-3ʹ), HNRNPK (Forward: 5ʹ-CAATGGTGAATTTGGTAAACGCC-3ʹ; Reverse: 5ʹ-GTAGTCTGTACGGAGAGCCTTA-3ʹ), β-actin (Forward: 5ʹ-CTCGCCTTTGCCGATCC-3ʹ; Reverse: 5ʹ-TCTCCATGTCGTCCCAGTTG-3ʹ), miR-873-5p (Forward: 5ʹ-GGGGCAGGAACTTGTGAG-3ʹ; Reverse: 5ʹ-GTGTGGTGTGGTATGGTGTG-3ʹ), and U6 small nuclear RNA (U6) (Forward: 5ʹ-CGCTTCGGCAGCACATATACTAAAATTGGAAC-3ʹ; Reverse: 5ʹ-GCTTCACGAATTTGCGTGTCATCCTTGC-3ʹ). Relative expression of circVPS33B, VPS33B mRNA, HNRNPK mRNA, and miR-873-5p was evaluated by 2−ΔΔCt method, and β-actin or U6 was used as an internal reference.
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2

Quantifying circVPS33B and miR-873-5p Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
RNAsimple Total RNA Kit from TIANGEN (Beijing, China) was utilized for total RNA separation (tissue samples and cells). The complementary DNA was synthesized with the M-MLV First Strand Kit (Life Technologies) or Bulge-Loop miR RT-qPCR Starter kit (RiboBio) and then used for qPCR with the SYBR Green (Solarbio). The primers were used as follows: circVPS33B (Forward: 5'-GTGGTGTTCTTGGGTGGTTGT-3'; Reverse: 5'-CCGCTCTAGCACCTTTCTCTC-3'), VPS33B (Forward: 5'-ATGAGCCCTTTGGATCGAATTG-3'; Reverse: 5'-ATGCGGGGTCTGACCAAGA-3'), HNRNPK (Forward: 5'-CAATGGTGAATTTGGTAAACGCC-3'; Reverse: 5'-GTAGTCTGTACGGAGAGCCTTA-3'), β-actin (Forward: 5'-GCACCACACCTTCTACAATG-3'; Reverse: 5'-TGCTTGCTGATCCACATCTG-3'), miR-873-5p (Forward: 5'-CGCATGGCAGTGGTTTTACCCTA-3'; Reverse: 5'-ATCCAGTGCAGGGTCCGAGG-3'), and U6 small nuclear RNA (U6) (Forward: 5'-CGCTTCGGCAGCACATATACTAAAATTGGAAC-3'; Reverse: 5'-GCTTCACGAATTTGCGTGTCATCCTTGC-3'). The levels of circVPS33B, VPS33B, HNRNPK, and miR-873-5p were evaluated by 2 -ΔΔCt method, and β-actin or U6 was used as an internal.
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3

Quantifying circVPS33B and miR-873-5p Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
RNAsimple Total RNA Kit from TIANGEN (Beijing, China) was utilized for total RNA separation (tissue samples and cells). The complementary DNA was synthesized with the M-MLV First Strand Kit (Life Technologies) or Bulge-Loop miR RT-qPCR Starter kit (RiboBio) and then used for qPCR with the SYBR Green (Solarbio). The primers were used as follows: circVPS33B (Forward: 5'-GTGGTGTTCTTGGGTGGTTGT-3'; Reverse: 5'-CCGCTCTAGCACCTTTCTCTC-3'), VPS33B (Forward: 5'-ATGAGCCCTTTGGATCGAATTG-3'; Reverse: 5'-ATGCGGGGTCTGACCAAGA-3'), HNRNPK (Forward: 5'-CAATGGTGAATTTGGTAAACGCC-3'; Reverse: 5'-GTAGTCTGTACGGAGAGCCTTA-3'), β-actin (Forward: 5'-GCACCACACCTTCTACAATG-3'; Reverse: 5'-TGCTTGCTGATCCACATCTG-3'), miR-873-5p (Forward: 5'-CGCATGGCAGTGGTTTTACCCTA-3'; Reverse: 5'-ATCCAGTGCAGGGTCCGAGG-3'), and U6 small nuclear RNA (U6) (Forward: 5'-CGCTTCGGCAGCACATATACTAAAATTGGAAC-3'; Reverse: 5'-GCTTCACGAATTTGCGTGTCATCCTTGC-3'). The levels of circVPS33B, VPS33B, HNRNPK, and miR-873-5p were evaluated by 2 -ΔΔCt method, and β-actin or U6 was used as an internal.
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