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small intestine total rna  (TaKaRa)


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  • 94

    Structured Review

    TaKaRa small intestine total rna
    Small Intestine Total Rna, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 141 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/small+intestine+rna/Human+Small+Intestine+Total+RNA/pmc13052076-251-21-25
    Average 94 stars, based on 141 article reviews
    small intestine total rna - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Expressing:

    Article Title: Regulation of the human apolipoprotein AIV gene expression in transgenic mice.
    Article Snippet: Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.. The two human hepatic and small intestine RNA samples were obtained from Clontech and Invitrogen.. Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.

    Northern Blot:

    Article Title: Regulation of the human apolipoprotein AIV gene expression in transgenic mice.
    Article Snippet: Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.. The two human hepatic and small intestine RNA samples were obtained from Clontech and Invitrogen.. Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.

    Transgenic Assay:

    Article Title: Regulation of the human apolipoprotein AIV gene expression in transgenic mice.
    Article Snippet: Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.. The two human hepatic and small intestine RNA samples were obtained from Clontech and Invitrogen.. Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.

    Isolation:

    Article Title: Regulation of the human apolipoprotein AIV gene expression in transgenic mice.
    Article Snippet: Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.. The two human hepatic and small intestine RNA samples were obtained from Clontech and Invitrogen.. Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.

    Control:

    Article Title: Regulation of the human apolipoprotein AIV gene expression in transgenic mice.
    Article Snippet: Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.Using the primer pair for L-actin ampli¢cation PCR was performed using 2 Wg of RNA to check that no contaminating genomic DNA remained.. The two human hepatic and small intestine RNA samples were obtained from Clontech and Invitrogen.. Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.Each sample derives from a di¡erent individual and is the same used for the commercial poly(A) blots obtained from the same suppliers.



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    TaKaRa adult small intestine asi
    Fig. 1. Differentiation of human iPSCs into intestinal organoids (IOs). (A) A schematic drawing of the overall culture timeline of iPSCs to establish IOs, showing respective culture platforms, matrices, and key molecules at each stage of differentiation. (B) Bright-field images of iPSC-derived differentiated cells. (Upper) Bright- field images showing iPSCs in 3D cluster microwell culture (day 0, 3, 8) (Representative 2 wells are shown). (Lower) iPSC-derived IOs (iPSC-IOs) formed in Matrigel- based culture on differentiation days 15, 22, and 29. (Right table) Cell growth rates in passage 1 (P1) on day 22 (d22) and P2 on d29 are shown as fold-change in cell numbers after 7 days of culture versus the starting cell no. of 1.0 × 105 cells. Scale bars: 200 μm (upper), 500 μm (lower). (C) Relative gene expression level of marker genes analyzed by qPCR on day 0 (before differentiation), day 3 (endoderm), day 8 (mid-/hind-gut), day 15 (P0), day 22 (P1), and day 29 (P2) are shown. The qPCR data are normalized against the adult <t>small</t> <t>intestine</t> <t>(ASI</t> = 1). Data are expressed as the mean ± SD (standard deviation), N = 3. Significances are shown as *p < 0.05, or **p < 0.01, by Dunnett’s multiple comparisons tests compared with control ASI in each gene set.
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    Image Search Results


    Fig. 1. Differentiation of human iPSCs into intestinal organoids (IOs). (A) A schematic drawing of the overall culture timeline of iPSCs to establish IOs, showing respective culture platforms, matrices, and key molecules at each stage of differentiation. (B) Bright-field images of iPSC-derived differentiated cells. (Upper) Bright- field images showing iPSCs in 3D cluster microwell culture (day 0, 3, 8) (Representative 2 wells are shown). (Lower) iPSC-derived IOs (iPSC-IOs) formed in Matrigel- based culture on differentiation days 15, 22, and 29. (Right table) Cell growth rates in passage 1 (P1) on day 22 (d22) and P2 on d29 are shown as fold-change in cell numbers after 7 days of culture versus the starting cell no. of 1.0 × 105 cells. Scale bars: 200 μm (upper), 500 μm (lower). (C) Relative gene expression level of marker genes analyzed by qPCR on day 0 (before differentiation), day 3 (endoderm), day 8 (mid-/hind-gut), day 15 (P0), day 22 (P1), and day 29 (P2) are shown. The qPCR data are normalized against the adult small intestine (ASI = 1). Data are expressed as the mean ± SD (standard deviation), N = 3. Significances are shown as *p < 0.05, or **p < 0.01, by Dunnett’s multiple comparisons tests compared with control ASI in each gene set.

    Journal: European journal of cell biology

    Article Title: Human pluripotent stem cell-derived intestinal organoids for pharmacokinetic studies.

    doi: 10.1016/j.ejcb.2025.151489

    Figure Lengend Snippet: Fig. 1. Differentiation of human iPSCs into intestinal organoids (IOs). (A) A schematic drawing of the overall culture timeline of iPSCs to establish IOs, showing respective culture platforms, matrices, and key molecules at each stage of differentiation. (B) Bright-field images of iPSC-derived differentiated cells. (Upper) Bright- field images showing iPSCs in 3D cluster microwell culture (day 0, 3, 8) (Representative 2 wells are shown). (Lower) iPSC-derived IOs (iPSC-IOs) formed in Matrigel- based culture on differentiation days 15, 22, and 29. (Right table) Cell growth rates in passage 1 (P1) on day 22 (d22) and P2 on d29 are shown as fold-change in cell numbers after 7 days of culture versus the starting cell no. of 1.0 × 105 cells. Scale bars: 200 μm (upper), 500 μm (lower). (C) Relative gene expression level of marker genes analyzed by qPCR on day 0 (before differentiation), day 3 (endoderm), day 8 (mid-/hind-gut), day 15 (P0), day 22 (P1), and day 29 (P2) are shown. The qPCR data are normalized against the adult small intestine (ASI = 1). Data are expressed as the mean ± SD (standard deviation), N = 3. Significances are shown as *p < 0.05, or **p < 0.01, by Dunnett’s multiple comparisons tests compared with control ASI in each gene set.

    Article Snippet: Total RNA of the human adult small intestine (ASI) (Takara Bio, Cat. No. 636539, Lot.

    Techniques: Derivative Assay, Gene Expression, Marker, Standard Deviation, Control