Fiber Shuttles Construction and Sequencing Primers

Jul 08, 2025

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This supplementary table provides a comprehensive list of primers essential for constructing and sequencing fiber shuttles in genetic studies. The primers listed here offer a valuable resource for researchers aiming to efficiently analyze fiber shuttle sequences.

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Fiber Shuttles Construction and Sequencing Primers

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Supplementary Table 3: Primers for constructing and sequencing Fiber Shuttles

Supplementary Table 1

Supplementary Table 1. Patient 1 2 3 4 5 6 7 8 9 10 11. Age (y) 44 36 34 40 26 36 35 48 33 48 35. Sex 1 M M M M F M M F M M M. Disease duration (y) 6 11 4 11 8 7 15 14 8 17 5. Disease classification 2 A2 L1 B3p A2 L1 B3p A2 L3 B3

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Supplementary Table S1. List of oligonucleotide primers used for amplification

Supplementary Table S1. List of oligonucleotide primers used for amplification of RSV RNA1 and RNA2 segments. Supplementary Table S2. GenBank accession numbers of RSV RNA 1 and RNA2 segments used in the study. Jonson et al. Supplementary Fig. S1. (A) RNA2 ORF1. (B) RNA2 ORF2. BA2-JB.

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Supplementary Table 1

Supplementary Table 1. A.

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Supplementary Table 5

Supplementary Table 5.

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Supplementary table 1.

Supplementary table 1. Strains used in this study. Strain. Genotype. Reference. ho∆ MAT α ::URA3::HOcs hml∆::ADE1 hmr∆::ADE1 ade1-100 leu2-3,112 lys5 trp1::hisG ura3-52 ade3::GAL::HO. SLY19. S. Lee et al. 2003.

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Supplementary Table 1:

Supplementary Table 1:.

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Supplementary Table 1

Supplementary Table 1. Primers used for qRT-PCR. Supplementary Table 2.

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Supplementary Table I . Gene-specific primers used for quantitatative real-time PCR

Supplementary Table I . Gene-specific primers used for quantitatative real-time PCR.

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Supplementary Table 2.

Supplementary Table 2. a The #CpG indicates the number of CpG in the sequence region. b The plus(+) and minus(-) indicate the presence and absence of CpG island, respectively. c The plus(+) and minus(-) indicate the presence and absence of candidate methylated site, respectively.

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Supplementary table 2

Supplementary table 2.

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Supplementary Table 2: Nucleotide sequence of primers used for PCR amplification

Supplementary Table 2: Nucleotide sequence of primers used for PCR amplification. Gene Accession no. Sequence cDNA Annealing Product Source

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Supplementary Table

Supplementary Table.

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Supplementary table 1

Supplementary table 1. Gene-expression values of LM f and LDC in microarray analysis were shown.

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Supplementary Table 1.

Supplementary Table 1. Selected reference drugs, testing concentrations and therapeutic exposure.

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Supplementary Table 2: Primers for constructing and sequencing pFex.

Supplementary Table 2: Primers for constructing and sequencing pFex. Supplementary Table 2.

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Supplementary Table 2.

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Supplementary table 1: Primers used for PCR amplification

Primer name. Sequence 5`-3`. Accession Number. ChiF. ACCAAGCTACTCGCAAGAGG. CD485880. ChiR. CGGAAGCGCAGTAAGATGA. GluF. CATTGATATGACCTTGATCG. CD486342. GluR. GTGAGATATCCCTTGGATTG. PR1F. TGCCCAAGACTCACAACAAG. CK988133.1 (Patil et al. 2005). PR1R. GGCCTTCTCATTAACCCACA. Hist3F.

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Supplementary Table 1 . List of primers used for real-time PCR analysis

Supplementary Table 1 . List of primers used for real-time PCR analysis. --------------------------------------------------------------------------------------------------------------------------------------- Gene Forward primer Reverse primer

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Supplementary Table 1 Sequences of quantative RT-PCR primers

Supplementary Table 1 Sequences of quantative RT-PCR primers. Supplementary Table 2 Body weight, plasma parameters and blood pressure of E-DNI  B mice. Supplementary Table 3 Body weight and plasma parameters of E-DNI  B mice. Supplementary Figure 1. Lung. Aorta. Macrophages.

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Supplementary Table

Antigen. Host. Isotype. Dilution. Source. Ankyrin G. Mouse. IgG1. 1:100. Zymed Labs San Francisco, CA. Caspr. Rabbit. IgG. 1:1000. E. Peles, Israel. Dystrophin. Mouse. IgG1. 1:200. Sigma Missouri, USA. FluoroMyelin green. -. -. 1:400. Molecular Probes Paisley, UK. Kv1.1.

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Supplementary Table 1

Supplementary Table 1. IC50 Value Matrix. Supplementary Table 1: IC 50 value matrix. Each cell line was treated with a dose range of 160 nM up to 1 µM of TAK-733, trametinib or vermurafenib and proliferation was measured using the SRB assay.

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Supplementary Table 1

Supplementary Table 1. Clinical Characteristics of human volunteers. Group I : Normal. Group II : CRS. Supplementary Table 2. Antibodies used for immunofluoresent microscopy. Supplementary Table 3. Antibodies used for mouse flow cytometry.

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