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human kidney total rna (TaKaRa)

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TaKaRa human kidney total rna
Human Kidney Total Rna, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 225 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+kidney+rna/Human+Kidney+Total+RNA/pmc13067571-108-6-10
Average 94 stars, based on 225 article reviews

human kidney total rna - by Bioz Stars, 2026-09

94/100 stars

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Article Title: Tumor-associated peptides binding to human leukocyte antigen (HLA) class II molecules
Article Snippet: Therefore, pooled healthy human kidney RNA was obtained commercially (Clontech, Heidelberg, Germany) and used as the baseline for these tumors.

Article Title: Enhanced Microvasculature Formation and Patterning in iPSC–Derived Kidney Organoids Cultured in Physiological Hypoxia
Article Snippet: Primer sequences ( ) were verified using total human kidney RNA (Takara Bio).

Article Title: Enhanced Microvasculature Formation and Patterning in iPSC-Derived Kidney Organoids Cultured in Physiological Hypoxia.
Article Snippet: Primer sequences (Supplementary Table S2) were verified using total human kidney RNA (Takara Bio).

Article Title: Differential uptake of arginine derivatives by the human heteromeric amino acid transporter b 0,+ AT-rBAT (SLC7A9-SLC3A1).
Article Snippet: Total human kidney RNA (purchased from Takara Bio Europe, Saint-Germain-en-Laye, France) was used as template for RT-PCR.

Article Title: Tumor-associated peptides binding promiscuously to human leukocyte antigen (HLA) class II molecules
Article Snippet: Therefore, pooled healthy human kidney RNA was obtained commercially (Clontech, Heidelberg, Germany) and used as the baseline for these tumors.

Article Title: Aberrant localization of β1 integrin in podocyte cytoplasm of primary FSGS with cellular lesion.
Article Snippet: For quantitative analysis, the levels were normalized to glyceraldehyde 3-phosphate dehydrogenase (GAPDH; Hs02786624_g1) in standard total human kidney RNA (Premium total RNA, 636,529; Clontech, Mountain View, CA, USA) using the ΔΔCt method (Ct indicates the threshold cycle).

Article Title: Aberrant localization of β1 integrin in podocyte cytoplasm of primary FSGS with cellular lesion
Article Snippet: For quantitative analysis, the levels were normalized to glyceraldehyde 3-phosphate dehydrogenase ( GAPDH ; Hs02786624_g1) in standard total human kidney RNA (Premium total RNA, 636,529; Clontech, Mountain View, CA, USA) using the ΔΔCt method (Ct indicates the threshold cycle).

Article Title: Differential uptake of arginine derivatives by the human heteromeric amino acid transporter b 0,+ AT-rBAT ( SLC7A9 - SLC3A1 )
Article Snippet: Total human kidney RNA (purchased from Takara Bio Europe, Saint-Germain-en-Laye, France) was used as template for RT-PCR.

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( A ) Detection of transglutaminases 3–7 by qPCR. Each lane corresponds to samples from one patient; diabetic ( D ) or non-diabetic (ND) status is indicated together with the age and sex. Positive controls (+) were RNA of human Skin (AH diagnostics) for TG3 and TG7, human prostate total RNA (AH diagnostics) for TG4, human kidney from samples for TG5, HK-2 (ATCC) cells for TG6. The used primers can be found in <xref ref-type=

Supplemental Table S3 . ( B ) Quantification of mRNA expression relative to GAPDH by qPCR ( B ) of TG2 (left) and eNOS (right) in subcutaneous artery samples of age-matched diabetic and non-diabetic patients. ( C ) Transamidase activity quantified by 5-BP incorporation, representative blots (above), and average log (5-BP incorporation) (arbitrary units) (below) in subcutaneous artery samples of age-matched diabetic and non-diabetic patients. Data are mean + SEM. " width="100%" height="100%">

Journal: Clinical Science (London, England : 1979)

Article Title: Sex-mediated effects of transglutaminase 2 inhibition on endothelial function in human resistance arteries from diabetic and non-diabetic patients

doi: 10.1042/CS20242001

Figure Lengend Snippet: ( A ) Detection of transglutaminases 3–7 by qPCR. Each lane corresponds to samples from one patient; diabetic ( D ) or non-diabetic (ND) status is indicated together with the age and sex. Positive controls (+) were RNA of human Skin (AH diagnostics) for TG3 and TG7, human prostate total RNA (AH diagnostics) for TG4, human kidney from samples for TG5, HK-2 (ATCC) cells for TG6. The used primers can be found in Supplemental Table S3 . ( B ) Quantification of mRNA expression relative to GAPDH by qPCR ( B ) of TG2 (left) and eNOS (right) in subcutaneous artery samples of age-matched diabetic and non-diabetic patients. ( C ) Transamidase activity quantified by 5-BP incorporation, representative blots (above), and average log (5-BP incorporation) (arbitrary units) (below) in subcutaneous artery samples of age-matched diabetic and non-diabetic patients. Data are mean + SEM.

Article Snippet: The positive controls for qPCR were human skin RNA (540031, AH Diagnostics) for TG3 and TG7, human prostate RNA (QS0624, AH Diagnostics) for TG4, human kidney RNA for TG5, and HK-2 cells (ATCC) for TG6.

Techniques: Expressing, Activity Assay