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multiple tissue northern blot analysis multiple normal human tissue blots mnhtb  (TaKaRa)


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    TaKaRa multiple tissue northern blot analysis multiple normal human tissue blots mnhtb
    Multiple Tissue Northern Blot Analysis Multiple Normal Human Tissue Blots Mnhtb, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 290 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+normalized+multiple+tissue+northern+blots/us08409566-981-0-14?v=TaKaRa
    Average 94 stars, based on 290 article reviews
    multiple tissue northern blot analysis multiple normal human tissue blots mnhtb - by Bioz Stars, 2026-07
    94/100 stars

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    Image Search Results


    Northern blots of poly(A)+ RNA from different human tissues were probed with a 491-bp fragment of human SERT cDNA (A). Arrows indicate RNA size markers (in bp). Higher exposure of ileum lane is shown in B.

    Journal: American journal of physiology. Gastrointestinal and liver physiology

    Article Title: Function, expression, and characterization of the serotonin transporter in the native human intestine

    doi: 10.1152/ajpgi.00354.2007

    Figure Lengend Snippet: Northern blots of poly(A)+ RNA from different human tissues were probed with a 491-bp fragment of human SERT cDNA (A). Arrows indicate RNA size markers (in bp). Higher exposure of ileum lane is shown in B.

    Article Snippet: To ascertain the presence of mRNA species encoding SERT in various human intestinal tissues, commercially available human multiple-tissue Northern blots (BioChain) were probed with 32 P-labeled 491-bp human SERT cDNA fragment.

    Techniques: Northern Blot

    Northern blot analysis of MAMDC1 mRNA expression in different human tissues, showing several expressed splice variants. MAMDC1 mRNA transcript corresponding to the full-length isoform is indicated by an arrowhead on the right side. A β-Actin cDNA control probe was used for normalization (bottom).

    Journal: PLoS ONE

    Article Title: Identification of MAMDC1 as a Candidate Susceptibility Gene for Systemic Lupus Erythematosus (SLE)

    doi: 10.1371/journal.pone.0008037

    Figure Lengend Snippet: Northern blot analysis of MAMDC1 mRNA expression in different human tissues, showing several expressed splice variants. MAMDC1 mRNA transcript corresponding to the full-length isoform is indicated by an arrowhead on the right side. A β-Actin cDNA control probe was used for normalization (bottom).

    Article Snippet: Fifty nano grams (ng) of purified cDNA were then labelled with P 32 -dCTP (GE Healthcare, Buckinghamshire, UK) by random priming and was used to probe two human multiple tissue polyA+ RNA Northern blots (HB2010 and HB2011, OriGene Technologies) according to manufacturer's instructions.

    Techniques: Northern Blot, Expressing, Control

    THP-1 cells were treated for 24 h with LPS, TGF-β1, IL-1β, IFN-γ, TNF-α, or a combination of TNF-α and IFN-γ, and MAMDC1 mRNA expression was quantified by Real-Time PCR in triplicate experiments. The results are reported as fold changes relative to THP-1 cells grown in the absence of stimulation (control), with the smallest observation, lower quartile, median, upper quartile, and largest observation shown for each sample.

    Journal: PLoS ONE

    Article Title: Identification of MAMDC1 as a Candidate Susceptibility Gene for Systemic Lupus Erythematosus (SLE)

    doi: 10.1371/journal.pone.0008037

    Figure Lengend Snippet: THP-1 cells were treated for 24 h with LPS, TGF-β1, IL-1β, IFN-γ, TNF-α, or a combination of TNF-α and IFN-γ, and MAMDC1 mRNA expression was quantified by Real-Time PCR in triplicate experiments. The results are reported as fold changes relative to THP-1 cells grown in the absence of stimulation (control), with the smallest observation, lower quartile, median, upper quartile, and largest observation shown for each sample.

    Article Snippet: Fifty nano grams (ng) of purified cDNA were then labelled with P 32 -dCTP (GE Healthcare, Buckinghamshire, UK) by random priming and was used to probe two human multiple tissue polyA+ RNA Northern blots (HB2010 and HB2011, OriGene Technologies) according to manufacturer's instructions.

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Control