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normal tissue human multiple tissue cdna panels  (TaKaRa)


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    TaKaRa normal tissue human multiple tissue cdna panels
    Normal Tissue Human Multiple Tissue Cdna Panels, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 592 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/normal tissue human multiple tissue cdna panels/product/TaKaRa
    Average 95 stars, based on 592 article reviews
    normal tissue human multiple tissue cdna panels - by Bioz Stars, 2026-05
    95/100 stars

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    MGC4607 expression analysis through use of RT-PCR. The expression of MGC4607 transcripts was analyzed by RT-PCR through use of the <t>cDNA</t> MTC1 <t>panel</t> <t>(Clontech).</t> Upper panel, MGC4607. Lower panel, β-actin. Lane 1,100-bp ladder. Lane 2, Brain. Lane 3, Heart. Lane 4, Skeletal muscle. Lane 5, Kidney. Lane 6, Liver. Lane 7, Pancreas. Lane 8, Lung. Lane 9, Placenta. In all tested cDNAs, two populations of MGC4607 transcripts existed, although at a different level, containing exon 2 (fragment from exons 1–6: 755 bp) or not containing exon 2 (fragment without exon 2: 581 bp).
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    MGC4607 expression analysis through use of RT-PCR. The expression of MGC4607 transcripts was analyzed by RT-PCR through use of the cDNA MTC1 panel (Clontech). Upper panel, MGC4607. Lower panel, β-actin. Lane 1,100-bp ladder. Lane 2, Brain. Lane 3, Heart. Lane 4, Skeletal muscle. Lane 5, Kidney. Lane 6, Liver. Lane 7, Pancreas. Lane 8, Lung. Lane 9, Placenta. In all tested cDNAs, two populations of MGC4607 transcripts existed, although at a different level, containing exon 2 (fragment from exons 1–6: 755 bp) or not containing exon 2 (fragment without exon 2: 581 bp).

    Journal:

    Article Title: Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations

    doi:

    Figure Lengend Snippet: MGC4607 expression analysis through use of RT-PCR. The expression of MGC4607 transcripts was analyzed by RT-PCR through use of the cDNA MTC1 panel (Clontech). Upper panel, MGC4607. Lower panel, β-actin. Lane 1,100-bp ladder. Lane 2, Brain. Lane 3, Heart. Lane 4, Skeletal muscle. Lane 5, Kidney. Lane 6, Liver. Lane 7, Pancreas. Lane 8, Lung. Lane 9, Placenta. In all tested cDNAs, two populations of MGC4607 transcripts existed, although at a different level, containing exon 2 (fragment from exons 1–6: 755 bp) or not containing exon 2 (fragment without exon 2: 581 bp).

    Article Snippet: Human normalized multiple-tissue cDNA (MTC I [Clontech]) panel and cDNA from control EBV lymphoblasts were amplified with these two MGC4607 primer pairs and with primers specific for the β-actin gene (forward, 5′-CCAGATCATGTTTGAGACCT-3′; and reverse, 5′-ACGTCACACTTCATGATGGA-3′).

    Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction

    MGC4607 northern blot analysis. Human adult MTN (human, 12 lanes [Clontech]) was hybridized with an MGC4607 (upper panel) and β-actin (lower panel) human cDNA probe. Lane 1, Brain. Lane 2, Heart. Lane 3, Skeletal muscle. Lane 4, Colon. Lane 5, Thymus. Lane 6, Spleen. Lane 7, Kidney. Lane 8, Liver. Lane 9, Small intestine. Lane 10, Placenta. Lane 11, Lung. Lane 12, Peripheral blood leukocytes. Expression of ∼1.8-kb MGC4607 transcripts was detected in all tissues studied.

    Journal:

    Article Title: Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations

    doi:

    Figure Lengend Snippet: MGC4607 northern blot analysis. Human adult MTN (human, 12 lanes [Clontech]) was hybridized with an MGC4607 (upper panel) and β-actin (lower panel) human cDNA probe. Lane 1, Brain. Lane 2, Heart. Lane 3, Skeletal muscle. Lane 4, Colon. Lane 5, Thymus. Lane 6, Spleen. Lane 7, Kidney. Lane 8, Liver. Lane 9, Small intestine. Lane 10, Placenta. Lane 11, Lung. Lane 12, Peripheral blood leukocytes. Expression of ∼1.8-kb MGC4607 transcripts was detected in all tissues studied.

    Article Snippet: Human normalized multiple-tissue cDNA (MTC I [Clontech]) panel and cDNA from control EBV lymphoblasts were amplified with these two MGC4607 primer pairs and with primers specific for the β-actin gene (forward, 5′-CCAGATCATGTTTGAGACCT-3′; and reverse, 5′-ACGTCACACTTCATGATGGA-3′).

    Techniques: Northern Blot, Expressing