SRX8858010 GSM4704970 SRP274535 SRS7120076 GSM4704970 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704970 GSM4704970 GEO Accession GSM4704970 SRX8858011 GSM4704971 SRP274535 SRS7120077 GSM4704971 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704971 GSM4704971 GEO Accession GSM4704971 SRX8858012 GSM4704972 SRP274535 SRS7120078 GSM4704972 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704972 GSM4704972 GEO Accession GSM4704972 SRX8858013 GSM4704973 SRP274535 SRS7120079 GSM4704973 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704973 GSM4704973 GEO Accession GSM4704973 SRX8858014 GSM4704974 SRP274535 SRS7120080 GSM4704974 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704974 GSM4704974 GEO Accession GSM4704974 SRX8858015 GSM4704975 SRP274535 SRS7120081 GSM4704975 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704975 GSM4704975 GEO Accession GSM4704975 SRX8858016 GSM4704976 SRP274535 SRS7120082 GSM4704976 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704976 GSM4704976 GEO Accession GSM4704976 SRX8858017 GSM4704977 SRP274535 SRS7120083 GSM4704977 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704977 GSM4704977 GEO Accession GSM4704977 SRX8858018 GSM4704978 SRP274535 SRS7120084 GSM4704978 RIP-Seq TRANSCRIPTOMIC other For immunoprecipitation of hnRNPC RNA complexes, 100 mg tissue from the human heart apex was used for each IP and control sample.After thawing, heart samples were washed, dissected, cross-linked and mechanically homogenized in lysis buffer. After sonication the sample was centrifuged and the supernatant was incubated O.N with antibody-conjugated-magnetic beads. After 3 washes reverse cross-linking was performed and proteins were digested by Proteinase K. RNA was extracted following TRIzol extraction protocol. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 550 gds 304704978 GSM4704978 GEO Accession GSM4704978