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marathon ready human brain cdna library  (TaKaRa)


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    Structured Review

    TaKaRa marathon ready human brain cdna library
    Molecular cloning of <t>novel</t> <t>RGS6</t> splice forms from human brain. ( A ) Splicing diagram of known RGS6 splice forms. Location of primers used for PCR-based amplification of RGS6 transcripts from a human whole brain <t>cDNA</t> library are shown in red. ( B ) Representative plasmid restriction digest (right) or nested PCR (down) indicating positive hits whose size is larger than known RGS6 splice forms. Each gel has a confirmed RGS6Lα1(+GGL) transcript (largest known splice form) indicated as well as yellow asterisks denoting transcripts encoding RGS6LA3α1(+GGL) which encodes RGS6B.
    Marathon Ready Human Brain Cdna Library, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 47 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+brain+cdna/Human+Pancreas+Marathon+-Ready+cDNA/bio_rxiv__64898__2026__05__08__723811-52-11-17
    Average 94 stars, based on 47 article reviews
    marathon ready human brain cdna library - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Molecular cloning of a novel, nervous system-specific RGS6 isoform lacking canonical G protein regulatory effects and with dominant negative actions"

    Article Title: Molecular cloning of a novel, nervous system-specific RGS6 isoform lacking canonical G protein regulatory effects and with dominant negative actions

    Journal: bioRxiv

    doi: 10.64898/2026.05.08.723811

    Molecular cloning of novel RGS6 splice forms from human brain. ( A ) Splicing diagram of known RGS6 splice forms. Location of primers used for PCR-based amplification of RGS6 transcripts from a human whole brain cDNA library are shown in red. ( B ) Representative plasmid restriction digest (right) or nested PCR (down) indicating positive hits whose size is larger than known RGS6 splice forms. Each gel has a confirmed RGS6Lα1(+GGL) transcript (largest known splice form) indicated as well as yellow asterisks denoting transcripts encoding RGS6LA3α1(+GGL) which encodes RGS6B.
    Figure Legend Snippet: Molecular cloning of novel RGS6 splice forms from human brain. ( A ) Splicing diagram of known RGS6 splice forms. Location of primers used for PCR-based amplification of RGS6 transcripts from a human whole brain cDNA library are shown in red. ( B ) Representative plasmid restriction digest (right) or nested PCR (down) indicating positive hits whose size is larger than known RGS6 splice forms. Each gel has a confirmed RGS6Lα1(+GGL) transcript (largest known splice form) indicated as well as yellow asterisks denoting transcripts encoding RGS6LA3α1(+GGL) which encodes RGS6B.

    Techniques Used: Molecular Cloning, Amplification, cDNA Library Assay, Plasmid Preparation, Nested PCR

    RGS6B is an RGS6L(+GGL) isoform containing A3 and the α terminal exon (RGS6LA3α1(+GGL)). ( A ) Schematic diagram of the exon splicing scheme comparing RGS6Lα1(+GGL) (RGS6L) and RGS6LA3α1(+GGL) (RGS6B). mRNA sequence conservation of exon A3 between mouse and human is depicted below with the consensus sequence from 100 vertebrate species extracted by PhyloP. PCR amplification of exon A3 containing mRNA transcripts from select mouse tissues ( B ) or human cDNA libraries ( C ). Plasmids encoding RGS6Lα1, RGS6Lα2 and RGS6LA3α1 (all +GGL) are used as negative and positive controls, respectively. LNG, lung; KDN, kidney; LVR, liver; SPL, spleen; CTX, cortex; MB, midbrain; CRB, cerebellum; HIP, hippocampus; MSC, muscle; HRT, heart; PNC, peripheral nervous system; BR, whole brain. ( D ) HEK293T cells were transfected with a plasmid encoding RGS6LA3α1(+GGL) to confirm co-migration with mouse RGS6B via immunoblotting. ( E ) shRNA or miRNA constructs targeting the A3 exon were introduced into mouse primary cortical astrocytes. The ratio of RGS6B: RGS6L was determined via immunoblot and quantified from 4 independent experiments. α Tubulin serves as a loading control for immunoblots. Data were analyzed by one sample t-test to detect deviation of each group from 100% (scramble RNAi control). *P<0.05, ***P<0.001. Data are expressed as mean ± S.E.M.
    Figure Legend Snippet: RGS6B is an RGS6L(+GGL) isoform containing A3 and the α terminal exon (RGS6LA3α1(+GGL)). ( A ) Schematic diagram of the exon splicing scheme comparing RGS6Lα1(+GGL) (RGS6L) and RGS6LA3α1(+GGL) (RGS6B). mRNA sequence conservation of exon A3 between mouse and human is depicted below with the consensus sequence from 100 vertebrate species extracted by PhyloP. PCR amplification of exon A3 containing mRNA transcripts from select mouse tissues ( B ) or human cDNA libraries ( C ). Plasmids encoding RGS6Lα1, RGS6Lα2 and RGS6LA3α1 (all +GGL) are used as negative and positive controls, respectively. LNG, lung; KDN, kidney; LVR, liver; SPL, spleen; CTX, cortex; MB, midbrain; CRB, cerebellum; HIP, hippocampus; MSC, muscle; HRT, heart; PNC, peripheral nervous system; BR, whole brain. ( D ) HEK293T cells were transfected with a plasmid encoding RGS6LA3α1(+GGL) to confirm co-migration with mouse RGS6B via immunoblotting. ( E ) shRNA or miRNA constructs targeting the A3 exon were introduced into mouse primary cortical astrocytes. The ratio of RGS6B: RGS6L was determined via immunoblot and quantified from 4 independent experiments. α Tubulin serves as a loading control for immunoblots. Data were analyzed by one sample t-test to detect deviation of each group from 100% (scramble RNAi control). *P<0.05, ***P<0.001. Data are expressed as mean ± S.E.M.

    Techniques Used: Sequencing, Amplification, Transfection, Plasmid Preparation, Migration, Western Blot, shRNA, Construct, Control

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    Clone Assay:

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    Article Snippet: .. The human PITPNA was cloned from human brain cDNA (Clontech) using PCR amplification and subcloned into pEGFP- C1 (all of PCR primers are listed in Table EV1). .. The human PITPNB (accession number BC018704, clone number 4643509 purchased from Open Biosystems) was also subcloned into pEGFPC1, and a ten amino acid residue linker (GGAGGAAAGA) was inserted between the EGFP tag and the PITPNB protein (synthesized as an oligomer pair).

    Article Title: Non-vesicular phosphatidylinositol transfer plays critical roles in defining organelle lipid composition
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    Polymerase Chain Reaction:

    Article Title: Non-vesicular phosphatidylinositol transfer plays critical roles in defining organelle lipid composition.
    Article Snippet: .. The human PITPNA was cloned from human brain cDNA (Clontech) using PCR amplification and subcloned into pEGFP- C1 (all of PCR primers are listed in Table EV1). .. The human PITPNB (accession number BC018704, clone number 4643509 purchased from Open Biosystems) was also subcloned into pEGFPC1, and a ten amino acid residue linker (GGAGGAAAGA) was inserted between the EGFP tag and the PITPNB protein (synthesized as an oligomer pair).

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    Article Snippet: Total RNA was extracted using the Qiagen RNeasy kit according to the manufacturer’s protocol, with β- mercaptoethanol added to buffer RLT and with a deoxyribonuclease (DNase) digestion step included. cDNA synthesis A total of 250 ng of RNA was used per sample for reverse transcription. .. Two different cDNA synthesis approaches were used: (i) Human brain cDNA was generated by SMARTer PCR cDNA synthesis (Takara) and (ii) iPSC- derived cell lines were generated using NEBNext Single Cell/Low Input cDNA Synthesis & Amplification Module (New England Biolabs). ..

    Article Title: The diversity of SNCA transcripts in neurons, and its impact on antisense oligonucleotide therapeutics
    Article Snippet: .. Two different cDNA synthesis approaches were used: (i) iPSC derived cell lines were generated using NEBNext® Single Cell/Low Input cDNA Synthesis & Amplification Module (New England Biolabs) and (ii) Human brain cDNA was generated by SMARTer PCR cDNA synthesis (Takara). ..

    Article Title: The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1
    Article Snippet: .. Two different cDNA synthesis approaches were used: (i) Human brain cDNA was generated by SMARTer PCR cDNA synthesis (Takara) and (ii) iPSC-derived cell lines were generated using NEBNext Single Cell/Low Input cDNA Synthesis & Amplification Module (New England Biolabs). ..

    Article Title: Compositions and methods for diagnosis and treatment of epilepsy
    Article Snippet: .. Primers will be designed to amplify the complete open reading frame of EFHC1 from human brain cDNA (Clontech) by PCR using PyrobestTM. .. The PCR product will be cloned into pEGFPC2 (Clontech) or pcDNA3.1 MycHis (Invitrogen) vector.

    Article Title: Non-vesicular phosphatidylinositol transfer plays critical roles in defining organelle lipid composition
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    Amplification:

    Article Title: Non-vesicular phosphatidylinositol transfer plays critical roles in defining organelle lipid composition.
    Article Snippet: .. The human PITPNA was cloned from human brain cDNA (Clontech) using PCR amplification and subcloned into pEGFP- C1 (all of PCR primers are listed in Table EV1). .. The human PITPNB (accession number BC018704, clone number 4643509 purchased from Open Biosystems) was also subcloned into pEGFPC1, and a ten amino acid residue linker (GGAGGAAAGA) was inserted between the EGFP tag and the PITPNB protein (synthesized as an oligomer pair).

    Article Title: The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1 .
    Article Snippet: Total RNA was extracted using the Qiagen RNeasy kit according to the manufacturer’s protocol, with β- mercaptoethanol added to buffer RLT and with a deoxyribonuclease (DNase) digestion step included. cDNA synthesis A total of 250 ng of RNA was used per sample for reverse transcription. .. Two different cDNA synthesis approaches were used: (i) Human brain cDNA was generated by SMARTer PCR cDNA synthesis (Takara) and (ii) iPSC- derived cell lines were generated using NEBNext Single Cell/Low Input cDNA Synthesis & Amplification Module (New England Biolabs). ..

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    cDNA Synthesis:

    Article Title: The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1 .
    Article Snippet: Total RNA was extracted using the Qiagen RNeasy kit according to the manufacturer’s protocol, with β- mercaptoethanol added to buffer RLT and with a deoxyribonuclease (DNase) digestion step included. cDNA synthesis A total of 250 ng of RNA was used per sample for reverse transcription. .. Two different cDNA synthesis approaches were used: (i) Human brain cDNA was generated by SMARTer PCR cDNA synthesis (Takara) and (ii) iPSC- derived cell lines were generated using NEBNext Single Cell/Low Input cDNA Synthesis & Amplification Module (New England Biolabs). ..

    Article Title: The diversity of SNCA transcripts in neurons, and its impact on antisense oligonucleotide therapeutics
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    Generated:

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    Derivative Assay:

    Article Title: The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1 .
    Article Snippet: Total RNA was extracted using the Qiagen RNeasy kit according to the manufacturer’s protocol, with β- mercaptoethanol added to buffer RLT and with a deoxyribonuclease (DNase) digestion step included. cDNA synthesis A total of 250 ng of RNA was used per sample for reverse transcription. .. Two different cDNA synthesis approaches were used: (i) Human brain cDNA was generated by SMARTer PCR cDNA synthesis (Takara) and (ii) iPSC- derived cell lines were generated using NEBNext Single Cell/Low Input cDNA Synthesis & Amplification Module (New England Biolabs). ..

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    Image Search Results


    Molecular cloning of novel RGS6 splice forms from human brain. ( A ) Splicing diagram of known RGS6 splice forms. Location of primers used for PCR-based amplification of RGS6 transcripts from a human whole brain cDNA library are shown in red. ( B ) Representative plasmid restriction digest (right) or nested PCR (down) indicating positive hits whose size is larger than known RGS6 splice forms. Each gel has a confirmed RGS6Lα1(+GGL) transcript (largest known splice form) indicated as well as yellow asterisks denoting transcripts encoding RGS6LA3α1(+GGL) which encodes RGS6B.

    Journal: bioRxiv

    Article Title: Molecular cloning of a novel, nervous system-specific RGS6 isoform lacking canonical G protein regulatory effects and with dominant negative actions

    doi: 10.64898/2026.05.08.723811

    Figure Lengend Snippet: Molecular cloning of novel RGS6 splice forms from human brain. ( A ) Splicing diagram of known RGS6 splice forms. Location of primers used for PCR-based amplification of RGS6 transcripts from a human whole brain cDNA library are shown in red. ( B ) Representative plasmid restriction digest (right) or nested PCR (down) indicating positive hits whose size is larger than known RGS6 splice forms. Each gel has a confirmed RGS6Lα1(+GGL) transcript (largest known splice form) indicated as well as yellow asterisks denoting transcripts encoding RGS6LA3α1(+GGL) which encodes RGS6B.

    Article Snippet: Full-length cDNAs encoding novel RGS6 splice forms were amplified from a Marathon ready human brain cDNA library (Clontech; Mountain View, CA, USA) using a PCR-based strategy.

    Techniques: Molecular Cloning, Amplification, cDNA Library Assay, Plasmid Preparation, Nested PCR

    RGS6B is an RGS6L(+GGL) isoform containing A3 and the α terminal exon (RGS6LA3α1(+GGL)). ( A ) Schematic diagram of the exon splicing scheme comparing RGS6Lα1(+GGL) (RGS6L) and RGS6LA3α1(+GGL) (RGS6B). mRNA sequence conservation of exon A3 between mouse and human is depicted below with the consensus sequence from 100 vertebrate species extracted by PhyloP. PCR amplification of exon A3 containing mRNA transcripts from select mouse tissues ( B ) or human cDNA libraries ( C ). Plasmids encoding RGS6Lα1, RGS6Lα2 and RGS6LA3α1 (all +GGL) are used as negative and positive controls, respectively. LNG, lung; KDN, kidney; LVR, liver; SPL, spleen; CTX, cortex; MB, midbrain; CRB, cerebellum; HIP, hippocampus; MSC, muscle; HRT, heart; PNC, peripheral nervous system; BR, whole brain. ( D ) HEK293T cells were transfected with a plasmid encoding RGS6LA3α1(+GGL) to confirm co-migration with mouse RGS6B via immunoblotting. ( E ) shRNA or miRNA constructs targeting the A3 exon were introduced into mouse primary cortical astrocytes. The ratio of RGS6B: RGS6L was determined via immunoblot and quantified from 4 independent experiments. α Tubulin serves as a loading control for immunoblots. Data were analyzed by one sample t-test to detect deviation of each group from 100% (scramble RNAi control). *P<0.05, ***P<0.001. Data are expressed as mean ± S.E.M.

    Journal: bioRxiv

    Article Title: Molecular cloning of a novel, nervous system-specific RGS6 isoform lacking canonical G protein regulatory effects and with dominant negative actions

    doi: 10.64898/2026.05.08.723811

    Figure Lengend Snippet: RGS6B is an RGS6L(+GGL) isoform containing A3 and the α terminal exon (RGS6LA3α1(+GGL)). ( A ) Schematic diagram of the exon splicing scheme comparing RGS6Lα1(+GGL) (RGS6L) and RGS6LA3α1(+GGL) (RGS6B). mRNA sequence conservation of exon A3 between mouse and human is depicted below with the consensus sequence from 100 vertebrate species extracted by PhyloP. PCR amplification of exon A3 containing mRNA transcripts from select mouse tissues ( B ) or human cDNA libraries ( C ). Plasmids encoding RGS6Lα1, RGS6Lα2 and RGS6LA3α1 (all +GGL) are used as negative and positive controls, respectively. LNG, lung; KDN, kidney; LVR, liver; SPL, spleen; CTX, cortex; MB, midbrain; CRB, cerebellum; HIP, hippocampus; MSC, muscle; HRT, heart; PNC, peripheral nervous system; BR, whole brain. ( D ) HEK293T cells were transfected with a plasmid encoding RGS6LA3α1(+GGL) to confirm co-migration with mouse RGS6B via immunoblotting. ( E ) shRNA or miRNA constructs targeting the A3 exon were introduced into mouse primary cortical astrocytes. The ratio of RGS6B: RGS6L was determined via immunoblot and quantified from 4 independent experiments. α Tubulin serves as a loading control for immunoblots. Data were analyzed by one sample t-test to detect deviation of each group from 100% (scramble RNAi control). *P<0.05, ***P<0.001. Data are expressed as mean ± S.E.M.

    Article Snippet: Full-length cDNAs encoding novel RGS6 splice forms were amplified from a Marathon ready human brain cDNA library (Clontech; Mountain View, CA, USA) using a PCR-based strategy.

    Techniques: Sequencing, Amplification, Transfection, Plasmid Preparation, Migration, Western Blot, shRNA, Construct, Control