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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/marathon+ready+cdna+library/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

    Related Articles

    cDNA Library Assay:

    Article Title: Nucleic acid molecules encoding transmembrane serine proteases, the encoded proteins and methods based thereon
    Article Snippet: .. The Marathon-Ready cDNA library from human liver (CLONTECH) was used to isolate the 5′ and 3′ ends of the cDNA encoding MTSP4. ..

    Article Title: Polypeptide having heparanase activity
    Article Snippet: Genomic sequence analysis: Large-scale sequencing was performed by Commonwealth Biotechnology Incorporation. .. Isolation of mouse hpa: Mouse hpa cDNA was amplified from either Marathon ready cDNA library of mouse embryo or from mRNA isolated from mouse melanoma cell line BL6, using the Marathon RACE kit from Clontech. ..

    Article Title: Facilitated Cross-Bridge Interactions with Thin Filaments by Familial Hypertrophic Cardiomyopathy Mutations in α -Tropomyosin
    Article Snippet: .. Full-length human α -Tm (accession no. M19713) and, for comparison in structural assays, β -Tm (accession no. X06825) cDNAs were PCR amplified from a Marathon-Ready cDNA Library (CLONTECH Laboratories Inc., Palo Alto, Calif, USA) made from human cardiac tissue. ..

    Article Title: Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1.
    Article Snippet: .. On the basis of this sequence, a 5 -rapid amplification of cDNA-ends-polymerase chain reaction (RACE-PCR) and a 3 -RACE-PCR were carried out with the reverse primers 5 -TGGCTCCTGCAATGGTGA-3 and 5 -TCCTCTGTTCCTGGTGTTTCT-3 , and the forward primers 5 -TTCTTTTGGGTGTTGACGG-3 and 5 -TTCCAAGGCCTCCTGTTACT-3 using the rat kidneyderived adaptor-ligated Marathon-Ready cDNA library (Clontech, Palo Alto, CA) according to the manufacturer’s instructions. ..

    Article Title: Nucleic acid molecules encoding transmembrane serine proteases, the encoded proteins and methods based thereon
    Article Snippet: .. The Marathon-Ready cDNA library from human liver (CLONTECH) was used to isolate the 5′ and 3′ ends of the cDNA encoding MTSP4. ..

    Article Title: Expression of a thyroglobulin (Tg) variant in mouse kidney glomerulus.
    Article Snippet: Thyroglobulin (Tg) is an essential substrate for thyroid hormone biosynthesis whose production is primarily limited to the thyroid follicular cell.. We have previously identified an 1.2 kb fragment of Tg mRNA in cultured mouse mesangial cells, and in the present study provide evidence showing that this transcript is transcribed and translated into a unique protein (kTg) in the kidney, but not the thyroid gland.. Cloning of kTg from a mouse kidney cDNA library showed that transcription starts in the middle of intron 41 of the Tg gene and continues in-frame with the remaining coding sequence of thyroidderived Tg beginning with exon 42.

    Article Title: Human E3α ubiquitin ligase family
    Article Snippet: PCR was carried out as described in Example 1 with the Marathon-Ready cDNA library (Clontech cat no. 7413-1) from which huE3αI cDNA was cloned. .. PCR was carried out as described in Example 1 with the Marathon-Ready cDNA library (Clontech cat no. 7413-1) from which huE3αI cDNA was cloned. ..

    Isolation:

    Article Title: Polypeptide having heparanase activity
    Article Snippet: Genomic sequence analysis: Large-scale sequencing was performed by Commonwealth Biotechnology Incorporation. .. Isolation of mouse hpa: Mouse hpa cDNA was amplified from either Marathon ready cDNA library of mouse embryo or from mRNA isolated from mouse melanoma cell line BL6, using the Marathon RACE kit from Clontech. ..

    Amplification:

    Article Title: Polypeptide having heparanase activity
    Article Snippet: Genomic sequence analysis: Large-scale sequencing was performed by Commonwealth Biotechnology Incorporation. .. Isolation of mouse hpa: Mouse hpa cDNA was amplified from either Marathon ready cDNA library of mouse embryo or from mRNA isolated from mouse melanoma cell line BL6, using the Marathon RACE kit from Clontech. ..

    Article Title: Facilitated Cross-Bridge Interactions with Thin Filaments by Familial Hypertrophic Cardiomyopathy Mutations in α -Tropomyosin
    Article Snippet: .. Full-length human α -Tm (accession no. M19713) and, for comparison in structural assays, β -Tm (accession no. X06825) cDNAs were PCR amplified from a Marathon-Ready cDNA Library (CLONTECH Laboratories Inc., Palo Alto, Calif, USA) made from human cardiac tissue. ..

    Article Title: Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1.
    Article Snippet: .. On the basis of this sequence, a 5 -rapid amplification of cDNA-ends-polymerase chain reaction (RACE-PCR) and a 3 -RACE-PCR were carried out with the reverse primers 5 -TGGCTCCTGCAATGGTGA-3 and 5 -TCCTCTGTTCCTGGTGTTTCT-3 , and the forward primers 5 -TTCTTTTGGGTGTTGACGG-3 and 5 -TTCCAAGGCCTCCTGTTACT-3 using the rat kidneyderived adaptor-ligated Marathon-Ready cDNA library (Clontech, Palo Alto, CA) according to the manufacturer’s instructions. ..

    Comparison:

    Article Title: Facilitated Cross-Bridge Interactions with Thin Filaments by Familial Hypertrophic Cardiomyopathy Mutations in α -Tropomyosin
    Article Snippet: .. Full-length human α -Tm (accession no. M19713) and, for comparison in structural assays, β -Tm (accession no. X06825) cDNAs were PCR amplified from a Marathon-Ready cDNA Library (CLONTECH Laboratories Inc., Palo Alto, Calif, USA) made from human cardiac tissue. ..

    Polymerase Chain Reaction:

    Article Title: Facilitated Cross-Bridge Interactions with Thin Filaments by Familial Hypertrophic Cardiomyopathy Mutations in α -Tropomyosin
    Article Snippet: .. Full-length human α -Tm (accession no. M19713) and, for comparison in structural assays, β -Tm (accession no. X06825) cDNAs were PCR amplified from a Marathon-Ready cDNA Library (CLONTECH Laboratories Inc., Palo Alto, Calif, USA) made from human cardiac tissue. ..

    Article Title: Expression of a thyroglobulin (Tg) variant in mouse kidney glomerulus.
    Article Snippet: Thyroglobulin (Tg) is an essential substrate for thyroid hormone biosynthesis whose production is primarily limited to the thyroid follicular cell.. We have previously identified an 1.2 kb fragment of Tg mRNA in cultured mouse mesangial cells, and in the present study provide evidence showing that this transcript is transcribed and translated into a unique protein (kTg) in the kidney, but not the thyroid gland.. Cloning of kTg from a mouse kidney cDNA library showed that transcription starts in the middle of intron 41 of the Tg gene and continues in-frame with the remaining coding sequence of thyroidderived Tg beginning with exon 42.

    Article Title: Human E3α ubiquitin ligase family
    Article Snippet: PCR was carried out as described in Example 1 with the Marathon-Ready cDNA library (Clontech cat no. 7413-1) from which huE3αI cDNA was cloned. .. PCR was carried out as described in Example 1 with the Marathon-Ready cDNA library (Clontech cat no. 7413-1) from which huE3αI cDNA was cloned. ..

    Sequencing:

    Article Title: Identification and functional characterization of a novel human and rat riboflavin transporter, RFT1.
    Article Snippet: .. On the basis of this sequence, a 5 -rapid amplification of cDNA-ends-polymerase chain reaction (RACE-PCR) and a 3 -RACE-PCR were carried out with the reverse primers 5 -TGGCTCCTGCAATGGTGA-3 and 5 -TCCTCTGTTCCTGGTGTTTCT-3 , and the forward primers 5 -TTCTTTTGGGTGTTGACGG-3 and 5 -TTCCAAGGCCTCCTGTTACT-3 using the rat kidneyderived adaptor-ligated Marathon-Ready cDNA library (Clontech, Palo Alto, CA) according to the manufacturer’s instructions. ..

    Article Title: Expression of a thyroglobulin (Tg) variant in mouse kidney glomerulus.
    Article Snippet: Thyroglobulin (Tg) is an essential substrate for thyroid hormone biosynthesis whose production is primarily limited to the thyroid follicular cell.. We have previously identified an 1.2 kb fragment of Tg mRNA in cultured mouse mesangial cells, and in the present study provide evidence showing that this transcript is transcribed and translated into a unique protein (kTg) in the kidney, but not the thyroid gland.. Cloning of kTg from a mouse kidney cDNA library showed that transcription starts in the middle of intron 41 of the Tg gene and continues in-frame with the remaining coding sequence of thyroidderived Tg beginning with exon 42.

    other:

    Article Title: Nucleic acid molecules encoding transmembrane serine proteases, the encoded proteins and methods based thereon
    Article Snippet: Subsequent search of GenBank and SwissProt database for the EST sequence AI924527 and AI924182 did not show any matching sequence to MTSP1, indicating that the sequence contained in these EST clones AI924527 and AI924182 may be portions of a new serine protease. b. PCR Cloning of a cDNA Fragment of Another Membrane Type Serine Protease MTSP3 The double-stranded Marathon-ReadyTM cDNA library derived from human lung carcinoma (LX-1) was obtained from Clontech (Palo Alto, Calif.; catalog #7495-1) and used as a template.

    Clone Assay:

    Article Title: Human E3α ubiquitin ligase family
    Article Snippet: PCR was carried out as described in Example 1 with the Marathon-Ready cDNA library (Clontech cat no. 7413-1) from which huE3αI cDNA was cloned. .. PCR was carried out as described in Example 1 with the Marathon-Ready cDNA library (Clontech cat no. 7413-1) from which huE3αI cDNA was cloned. ..



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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