library construction Search Results


chromium single cell 50 library construction kit 10x genomics  (10X Genomics)
86
10X Genomics chromium single cell 50 library construction kit 10x genomics
Chromium Single Cell 50 Library Construction Kit 10x Genomics, supplied by 10X Genomics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pm35803246-711-53-60?v=10X+Genomics
Average 86 stars, based on 1 article reviews
chromium single cell 50 library construction kit 10x genomics - by Bioz Stars, 2026-07
86/100 stars
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fragments 10 kbp and a library was constructed using a ligation sequencing kit  (Oxford Nanopore)
97
Oxford Nanopore fragments 10 kbp and a library was constructed using a ligation sequencing kit
Fragments 10 Kbp And A Library Was Constructed Using A Ligation Sequencing Kit, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc11320934-39-18-31?v=Oxford+Nanopore
Average 97 stars, based on 1 article reviews
fragments 10 kbp and a library was constructed using a ligation sequencing kit - by Bioz Stars, 2026-07
97/100 stars
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rna-seq library construction  (GENterprise gmbh)
90
GENterprise gmbh rna-seq library construction
Rna Seq Library Construction, supplied by GENterprise gmbh, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc04352258-291-1-17?v=GENterprise+gmbh
Average 90 stars, based on 1 article reviews
rna-seq library construction - by Bioz Stars, 2026-07
90/100 stars
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library construction and sequencing  (WuXi AppTec)
90
WuXi AppTec library construction and sequencing
Library Construction And Sequencing, supplied by WuXi AppTec, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc04620451-192-3-7?v=WuXi+AppTec
Average 90 stars, based on 1 article reviews
library construction and sequencing - by Bioz Stars, 2026-07
90/100 stars
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cdna library construction protocols  (Oxford Nanopore)
90
Oxford Nanopore cdna library construction protocols
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Cdna Library Construction Protocols, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc10166177-347-7-15?v=Oxford+Nanopore
Average 90 stars, based on 1 article reviews
cdna library construction protocols - by Bioz Stars, 2026-07
90/100 stars
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library construction, sequencing and snp calling  (Floragenex)
90
Floragenex library construction, sequencing and snp calling
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Library Construction, Sequencing And Snp Calling, supplied by Floragenex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc06278636-108-4-9?v=Floragenex
Average 90 stars, based on 1 article reviews
library construction, sequencing and snp calling - by Bioz Stars, 2026-07
90/100 stars
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matchmaker library construction screening kits  (Becton Dickinson)
90
Becton Dickinson matchmaker library construction screening kits
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Matchmaker Library Construction Screening Kits, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc03252155-413-16-18?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
matchmaker library construction screening kits - by Bioz Stars, 2026-07
90/100 stars
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srna library construction and deep sequencing  (BGI Shenzhen)
90
BGI Shenzhen srna library construction and deep sequencing
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Srna Library Construction And Deep Sequencing, supplied by BGI Shenzhen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pm33568480-321-24-29?v=BGI+Shenzhen
Average 90 stars, based on 1 article reviews
srna library construction and deep sequencing - by Bioz Stars, 2026-07
90/100 stars
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cdna library construction and sequencing  (BGI Shenzhen)
90
BGI Shenzhen cdna library construction and sequencing
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Cdna Library Construction And Sequencing, supplied by BGI Shenzhen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc03679102-104-0-8?v=BGI+Shenzhen
Average 90 stars, based on 1 article reviews
cdna library construction and sequencing - by Bioz Stars, 2026-07
90/100 stars
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cdna sequencing  (LC Sciences)
90
LC Sciences cdna sequencing
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Cdna Sequencing, supplied by LC Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc04962988-68-3-16?v=LC+Sciences
Average 90 stars, based on 1 article reviews
cdna sequencing - by Bioz Stars, 2026-07
90/100 stars
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small rna library construction  (Arraystar inc)
90
Arraystar inc small rna library construction
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Small Rna Library Construction, supplied by Arraystar inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc08060202-83-0-12?v=Arraystar+inc
Average 90 stars, based on 1 article reviews
small rna library construction - by Bioz Stars, 2026-07
90/100 stars
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smart cdna construction kit  (Becton Dickinson)
90
Becton Dickinson smart cdna construction kit
DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing <t>and</t> <t>RNA</t> metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified <t>cDNA.</t> (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .
Smart Cdna Construction Kit, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/library+construction/pmc01434744-155-23-27?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
smart cdna construction kit - by Bioz Stars, 2026-07
90/100 stars
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Image Search Results


DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing and RNA metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified cDNA. (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .

Journal: Protein & Cell

Article Title: A molecular brake that modulates spliceosome pausing at detained introns contributes to neurodegeneration

doi: 10.1093/procel/pwac008

Figure Lengend Snippet: DI splicing is likely paused at B act . (A) Potential SNIP1 interacting proteins identified by Flag-IP coupled with mass spectrometry (co-IP/MS) in N2a cells expressing Flag-SNIP1. Many of these protein partners are involved in pre-mRNA splicing and RNA metabolism (also see ). (B) The potential SNIP1 interacting partners are found in B act but not B*. Factors loaded into B* are labeled in gray, which were not hit by our co-IP/MS. (C and D) Interactions between SNIP1 and protein components found in B act component SF3a120 (C) but not those in B* component YJU2 (D) were validated in N2a cells expressing the indicated tagged proteins. (E) RIP was performed in N2a cells expressing Flag-SF3a120, Flag-YJU2, or EGFP. DIs were measured by RT-PCR using Smart-amplified cDNA. (F–I) Flag-RIP-seq was performed in N2a cells expressing Flag-SF3a120 (F) and Flag-YJU2 (G). N2a cells expressing EGFP, a negative control for our Flag-RIP-seq. Two representative SF3a120-bound DIs visualized by IGV (H and I). See also , .

Article Snippet: Total RNA (1 μg) was used for cDNA library construction, following the protocols suggested by Oxford Nanopore Technologies (ONT).

Techniques: Mass Spectrometry, Co-Immunoprecipitation Assay, Expressing, Labeling, Reverse Transcription Polymerase Chain Reaction, Amplification, Negative Control