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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+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

    Plasmid Preparation:

    Article Title: Regulation of DNA Methylation Through EBP1 Interaction with NLRP2 and NLRP7
    Article Snippet: To screen for novel protein interactions, Y2H Gold yeast were transformed with one of the bait plasmids (pGBKT7-hNLRP2, and pGBKT7-hNLRP7) using the Frozen-EZ Yeast Transformation II Kit (Cat. T2001, Zymo Research, Irvine, CA, USA). .. Yeast containing the bait plasmid was mated with yeast containing a human cDNA library (Cat. 630479, Clontech, Mountain View, CA, USA) following the Matchmaker GAL4-based two-hybrid assay protocol (Cat. 630466, 630489, 630498, 630499). ..

    cDNA Library Assay:

    Article Title: Regulation of DNA Methylation Through EBP1 Interaction with NLRP2 and NLRP7
    Article Snippet: To screen for novel protein interactions, Y2H Gold yeast were transformed with one of the bait plasmids (pGBKT7-hNLRP2, and pGBKT7-hNLRP7) using the Frozen-EZ Yeast Transformation II Kit (Cat. T2001, Zymo Research, Irvine, CA, USA). .. Yeast containing the bait plasmid was mated with yeast containing a human cDNA library (Cat. 630479, Clontech, Mountain View, CA, USA) following the Matchmaker GAL4-based two-hybrid assay protocol (Cat. 630466, 630489, 630498, 630499). ..

    Article Title: Loss of GalNAc-T14 links O -glycosylation defects to alterations in B cell homing in IgA nephropathy
    Article Snippet: .. B A Supplemental Figure 1: Expression of GALNT14 in human tissues. (A) Using a commercially available human cDNA library (Multiple Tissue panel and Immune system panel by Clontech), expression of GALNT14 was highest in the human kidney. (B) GALNT14 gene expression in tissue from the GTEx database again demonstrating GALNT14 is highly expressed in the kidney. ..

    Article Title: A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment.
    Article Snippet: Gain-of-function variants in GFAP leads to protein aggregation and is the cause of the severe neurodegenerative disorder Alexander Disease (AxD), while loss of GFAP function has been considered benign.. Here, we investigated a six-generation family, where multiple individuals presented with gliosis of the optic nerve head and visual impairment.. Whole genome sequencing (WGS) revealed a frameshift variant in GFAP (c.928dup, p.(Met310Asnfs∗113)) segregating with disease.

    Article Title: Site-directed antibodies targeting driver mutations of the KRAS protein.
    Article Snippet: .. The wild-type KRAS gene was amplified from a human cDNA library (Cat. 637260, Takara Bio USA, Ann Arbor, MI, USA) using PCR Jo ur na l P re -p ro of Page 7 of 30 with primers GWP0042 and GWP0532 (Supplemental Table 1) producing a 441 bp insert fragment. ..

    Article Title: TSG101 Promotes SIAH1 Auto‐Ubiquitination to Drive Migration and Invasion in Hepatocellular Carcinoma Cells
    Article Snippet: The recombinant pGBK‐T7‐SIAH1 plasmid was transformed into yeast Y2HGold (Clontech, CA). .. The Y187 yeast containing human cDNA library (Cat No. 630486, Clontech) was hybridized with Y2HGold/pGBK‐T7‐SIAH1 and spread on the SD/−Leu/−Trp/X‐Gal/AbA (Aureobasidin A) (DDO/X/A) agar plate for screening. ..

    Article Title: Combinatorial ubiquitin code degrades deubiquitylation-protected substrates
    Article Snippet: K29-, K48-, or K63-linked ubiquitin chains and their conjugated proteins were enriched using GST-TRABID-NZF1 (UBPBio, #J4470), FLAG K48TUBE HF (LifeSensors, UM607), or FLAG K63TUBE (LifeSensors, UM604), respectively. .. The genes encoding E2E1, Ubc9, and Sae2 were PCR amplified from a human cDNA library (Clontech). .. GST-tagged TRABID NZF (40 μg), 1 μg of FLAG-tagged K48TUBE (LifeSensors, UM607), or 1 μg of FLAG-tagged K63TUBE (LifeSensors, UM604) were added to cell lysates to capture K29-, K48-, or K63-linked chains, respectively, and were precipitated using Glutathione Sepharose (GE Healthcare, 17-0756-01) or anti-FLAG affinity resin.

    Article Title: TSG101 Promotes SIAH1 Auto-Ubiquitination to Drive Migration and Invasion in Hepatocellular Carcinoma Cells.
    Article Snippet: The recombinant pGBK- T7- SIAH1 plasmid was transformed into yeast Y2HGold (Clontech, CA). .. The Y187 yeast containing human cDNA library (Cat No. 630486, Clontech) was hybridized with Y2HGold/pGBK- T7- SIAH1 and spread on the SD/−Leu/−Trp/X- Gal/AbA (Aureobasidin A) (DDO/X/A) agar plate for screening. ..

    Two Hybrid Assay:

    Article Title: Regulation of DNA Methylation Through EBP1 Interaction with NLRP2 and NLRP7
    Article Snippet: To screen for novel protein interactions, Y2H Gold yeast were transformed with one of the bait plasmids (pGBKT7-hNLRP2, and pGBKT7-hNLRP7) using the Frozen-EZ Yeast Transformation II Kit (Cat. T2001, Zymo Research, Irvine, CA, USA). .. Yeast containing the bait plasmid was mated with yeast containing a human cDNA library (Cat. 630479, Clontech, Mountain View, CA, USA) following the Matchmaker GAL4-based two-hybrid assay protocol (Cat. 630466, 630489, 630498, 630499). ..

    Expressing:

    Article Title: Loss of GalNAc-T14 links O -glycosylation defects to alterations in B cell homing in IgA nephropathy
    Article Snippet: .. B A Supplemental Figure 1: Expression of GALNT14 in human tissues. (A) Using a commercially available human cDNA library (Multiple Tissue panel and Immune system panel by Clontech), expression of GALNT14 was highest in the human kidney. (B) GALNT14 gene expression in tissue from the GTEx database again demonstrating GALNT14 is highly expressed in the kidney. ..

    Gene Expression:

    Article Title: Loss of GalNAc-T14 links O -glycosylation defects to alterations in B cell homing in IgA nephropathy
    Article Snippet: .. B A Supplemental Figure 1: Expression of GALNT14 in human tissues. (A) Using a commercially available human cDNA library (Multiple Tissue panel and Immune system panel by Clontech), expression of GALNT14 was highest in the human kidney. (B) GALNT14 gene expression in tissue from the GTEx database again demonstrating GALNT14 is highly expressed in the kidney. ..

    other:

    Article Title: Combinatorial ubiquitin code degrades deubiquitylation-protected substrates.
    Article Snippet: Peptides were separated on an analytical column (IonOpticks, same specifications as described earlier) using a 4 h gradient (0–28% acetonitrile over 240min).

    Amplification:

    Article Title: A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment.
    Article Snippet: Gain-of-function variants in GFAP leads to protein aggregation and is the cause of the severe neurodegenerative disorder Alexander Disease (AxD), while loss of GFAP function has been considered benign.. Here, we investigated a six-generation family, where multiple individuals presented with gliosis of the optic nerve head and visual impairment.. Whole genome sequencing (WGS) revealed a frameshift variant in GFAP (c.928dup, p.(Met310Asnfs∗113)) segregating with disease.

    Article Title: Site-directed antibodies targeting driver mutations of the KRAS protein.
    Article Snippet: .. The wild-type KRAS gene was amplified from a human cDNA library (Cat. 637260, Takara Bio USA, Ann Arbor, MI, USA) using PCR Jo ur na l P re -p ro of Page 7 of 30 with primers GWP0042 and GWP0532 (Supplemental Table 1) producing a 441 bp insert fragment. ..

    Article Title: Combinatorial ubiquitin code degrades deubiquitylation-protected substrates
    Article Snippet: K29-, K48-, or K63-linked ubiquitin chains and their conjugated proteins were enriched using GST-TRABID-NZF1 (UBPBio, #J4470), FLAG K48TUBE HF (LifeSensors, UM607), or FLAG K63TUBE (LifeSensors, UM604), respectively. .. The genes encoding E2E1, Ubc9, and Sae2 were PCR amplified from a human cDNA library (Clontech). .. GST-tagged TRABID NZF (40 μg), 1 μg of FLAG-tagged K48TUBE (LifeSensors, UM607), or 1 μg of FLAG-tagged K63TUBE (LifeSensors, UM604) were added to cell lysates to capture K29-, K48-, or K63-linked chains, respectively, and were precipitated using Glutathione Sepharose (GE Healthcare, 17-0756-01) or anti-FLAG affinity resin.

    Polymerase Chain Reaction:

    Article Title: Site-directed antibodies targeting driver mutations of the KRAS protein.
    Article Snippet: .. The wild-type KRAS gene was amplified from a human cDNA library (Cat. 637260, Takara Bio USA, Ann Arbor, MI, USA) using PCR Jo ur na l P re -p ro of Page 7 of 30 with primers GWP0042 and GWP0532 (Supplemental Table 1) producing a 441 bp insert fragment. ..

    Article Title: Combinatorial ubiquitin code degrades deubiquitylation-protected substrates
    Article Snippet: K29-, K48-, or K63-linked ubiquitin chains and their conjugated proteins were enriched using GST-TRABID-NZF1 (UBPBio, #J4470), FLAG K48TUBE HF (LifeSensors, UM607), or FLAG K63TUBE (LifeSensors, UM604), respectively. .. The genes encoding E2E1, Ubc9, and Sae2 were PCR amplified from a human cDNA library (Clontech). .. GST-tagged TRABID NZF (40 μg), 1 μg of FLAG-tagged K48TUBE (LifeSensors, UM607), or 1 μg of FLAG-tagged K63TUBE (LifeSensors, UM604) were added to cell lysates to capture K29-, K48-, or K63-linked chains, respectively, and were precipitated using Glutathione Sepharose (GE Healthcare, 17-0756-01) or anti-FLAG affinity resin.



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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