Review



iscript supermix reverse transcriptase kit  (Bio-Rad)


Bioz Verified Symbol Bio-Rad is a verified supplier
Bioz Manufacturer Symbol Bio-Rad manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    Bio-Rad iscript supermix reverse transcriptase kit
    Iscript Supermix Reverse Transcriptase Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/iscript+reverse+transcription+supermix/pmc04154239-111-28-33
    Average 90 stars, based on 1 article reviews
    iscript supermix reverse transcriptase kit - by Bioz Stars, 2026-11
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: Pyridine-Based Glycosides Bearing 1,2,4-Triazole and Their 1,3,4-oxadiazole analogues as Potential EGFR and CDK-2 Inhibitors: Design, Synthesis, Antiproliferative Activity and In Silico Studies
    Article Snippet: The increasing toxicity of recently developed anticancer medications is seen as a serious problem that stems from the variety of targets involved; as a result, more research on these phenomena is necessary.. In the present work, a novel class of pyridine-based glycosides with a 1,2,4-triazole core and their 1,3,4-oxadiazolyl counterparts with distinct sugar segments are designed and synthesized.. The afforded products were studied for their cytotoxicity behavior against a number of cell lines of human cancer.

    Article Title: Neutrophil extracellular traps, B cells, and type 1 Interferons contribute to immune dysregulation in Hidradenitis Suppurativa
    Article Snippet: Images were acquired on a Zeiss LSM780 confocal laser-scanner microscope.

    Article Title: Design of diverse, functional mitochondrial targeting sequences across eukaryotic organisms using variational autoencoder
    Article Snippet: The formation of a pink compound was observed and the absorbance was measured at 553 nm using a SpectraMax Mini Multi-mode microplate reader (Molecular Devices, USA).

    Tissue Homogenization:

    Article Title: Systemic inflammation following traumatic injury and its impact on neuroinflammatory gene expression in the rodent brain.
    Article Snippet: To evaluate clinically relevant serum biomarkers of end-organ damage, the serum levels of AST, ALT, BUN, and ALB, which are indicators of liver injury, and the concentration of creatinine (Cr), which is an indicator of kidney injury and function, were determined at 6, 24, and 168 hpi by using a fully automated clinical chemistry analyzer (Element DC5X Veterinary Chemistry Analyzer; Heska, Loveland, Colorado, USA). .. Snap-frozen biopsy samples (LN2) were thawed on ice and homogenized in 500 μL Qiazol solution using a ceramic bead tissue homogenization system (VWR, Radnor, PA, USA) and Total mRNA was isolated from each sample using the miRNeasy Mini kit (Qiagen, Valencia, CA, USA) and DNA contamination was removed using the RNase-free DNase Digestion kit (Qiagen, Valencia, CA, USA) solution applied to the miRNeasy column. cDNA was transcribed from brain biopsy specimens using iScript Advanced cDNA Reverse Transcriptase Kit (Bio-Rad, Hercules, CA, USA) [12, 44]. .. Total mRNA yields > 1 μg and an A260/280 ratio between 1.8 and 2.2 were considered sufficient in quantity and quality for further analysis. qPCR products were assessed by RT‒qPCR SYBR-Green fluorescence (SsoAdvanced Universal SYBR Green Supermix; Bio-Rad, Hercules, CA, USA) on custom low-density PCR arrays comprising 86 genes known to be associated with neuroinflammation (cytokineschemokines and their receptors), neurodegeneration, tissue damage, oxidative stress, apoptosis, and early transcriptional activators, in addition to five (B2m, Gapdh, Hprt1, Rplp0, Rplp2) suitable housekeeping genes, using a real-time qPCR machine (QuantStudio 7 Pro, Applied Biosystems, Foster City CA, USA).

    Isolation:

    Article Title: Systemic inflammation following traumatic injury and its impact on neuroinflammatory gene expression in the rodent brain.
    Article Snippet: To evaluate clinically relevant serum biomarkers of end-organ damage, the serum levels of AST, ALT, BUN, and ALB, which are indicators of liver injury, and the concentration of creatinine (Cr), which is an indicator of kidney injury and function, were determined at 6, 24, and 168 hpi by using a fully automated clinical chemistry analyzer (Element DC5X Veterinary Chemistry Analyzer; Heska, Loveland, Colorado, USA). .. Snap-frozen biopsy samples (LN2) were thawed on ice and homogenized in 500 μL Qiazol solution using a ceramic bead tissue homogenization system (VWR, Radnor, PA, USA) and Total mRNA was isolated from each sample using the miRNeasy Mini kit (Qiagen, Valencia, CA, USA) and DNA contamination was removed using the RNase-free DNase Digestion kit (Qiagen, Valencia, CA, USA) solution applied to the miRNeasy column. cDNA was transcribed from brain biopsy specimens using iScript Advanced cDNA Reverse Transcriptase Kit (Bio-Rad, Hercules, CA, USA) [12, 44]. .. Total mRNA yields > 1 μg and an A260/280 ratio between 1.8 and 2.2 were considered sufficient in quantity and quality for further analysis. qPCR products were assessed by RT‒qPCR SYBR-Green fluorescence (SsoAdvanced Universal SYBR Green Supermix; Bio-Rad, Hercules, CA, USA) on custom low-density PCR arrays comprising 86 genes known to be associated with neuroinflammation (cytokineschemokines and their receptors), neurodegeneration, tissue damage, oxidative stress, apoptosis, and early transcriptional activators, in addition to five (B2m, Gapdh, Hprt1, Rplp0, Rplp2) suitable housekeeping genes, using a real-time qPCR machine (QuantStudio 7 Pro, Applied Biosystems, Foster City CA, USA).

    Reverse Transcription:

    Article Title: Systemic inflammation following traumatic injury and its impact on neuroinflammatory gene expression in the rodent brain.
    Article Snippet: To evaluate clinically relevant serum biomarkers of end-organ damage, the serum levels of AST, ALT, BUN, and ALB, which are indicators of liver injury, and the concentration of creatinine (Cr), which is an indicator of kidney injury and function, were determined at 6, 24, and 168 hpi by using a fully automated clinical chemistry analyzer (Element DC5X Veterinary Chemistry Analyzer; Heska, Loveland, Colorado, USA). .. Snap-frozen biopsy samples (LN2) were thawed on ice and homogenized in 500 μL Qiazol solution using a ceramic bead tissue homogenization system (VWR, Radnor, PA, USA) and Total mRNA was isolated from each sample using the miRNeasy Mini kit (Qiagen, Valencia, CA, USA) and DNA contamination was removed using the RNase-free DNase Digestion kit (Qiagen, Valencia, CA, USA) solution applied to the miRNeasy column. cDNA was transcribed from brain biopsy specimens using iScript Advanced cDNA Reverse Transcriptase Kit (Bio-Rad, Hercules, CA, USA) [12, 44]. .. Total mRNA yields > 1 μg and an A260/280 ratio between 1.8 and 2.2 were considered sufficient in quantity and quality for further analysis. qPCR products were assessed by RT‒qPCR SYBR-Green fluorescence (SsoAdvanced Universal SYBR Green Supermix; Bio-Rad, Hercules, CA, USA) on custom low-density PCR arrays comprising 86 genes known to be associated with neuroinflammation (cytokineschemokines and their receptors), neurodegeneration, tissue damage, oxidative stress, apoptosis, and early transcriptional activators, in addition to five (B2m, Gapdh, Hprt1, Rplp0, Rplp2) suitable housekeeping genes, using a real-time qPCR machine (QuantStudio 7 Pro, Applied Biosystems, Foster City CA, USA).

    Article Title: Housing mice near vs. below thermoneutrality affects drug-induced weight loss but does not improve prediction of efficacy in humans
    Article Snippet: .. RNA was extracted using RNeasy Mini Kit (Cat. No. 74106, Qiagen, Hilden, Germany). cDNA was synthesized using iScript Reverse Transcription Supermix (Cat. No. 1708840, Bio-Rad Laboratories, inc. CA, USA) following manufacturer’s instructions. .. Gene expression was determined by quantitative real-time PCR on ViiA-7, using 1 ng of cDNA mixed with TaqMan OpenArray Real-Time PCR Master Mix (Applied Biosystems, Thermo Fisher Scientific, USA) and TaqMan probes listed in .

    Article Title: Tilorone mitigates the propagation of α-synucleinopathy in a midbrain-like organoid model
    Article Snippet: Total RNA was extracted from 10 brain organoid per each sample using TriPure reagent (Roche) and purified using RNeasy MinElute Cleanup Kit (Promega) following the standard protocols. .. The RNA concentration was measured by Nanodrop 2000 UV spectrophotometer, and 1 μg total RNA was converted to cDNA using the iScript Reverse Transcription Supermix (BioRad) system. ..

    Article Title: Manganese inhibits SVCV infection by promoting the expression of STING and the subsequent activation of IFN
    Article Snippet: Manganese (Mn) is necessary for various biological processes, yet its function in innate immunity has been less studied, especially in fish.. Stimulator of interferon (IFN) genes (STING) is an essential factor for IFN induction in virus infection.. Our study demonstrated that Mn2+ increases the ability of zebrafish to resist spring viraemia of carp virus (SVCV) infection by enhancing the expression of STING.

    Real-time Polymerase Chain Reaction:

    Article Title: Raffinose induces autophagy to promote plant growth
    Article Snippet: Finally, 200ng of total RNA was reverse transcribed with Superscript SentiFAST cDNA synthesis Kit (Bioline, London, UK). .. Real-time PCR reactions were performed in BIO-RAD HARD SHELL 96 well PCR Plates, using SYBR Green PCR Master Mix in the qRT-PCR (CFX Duet 96-well; Bio-Rad, Hercules, CA, USA). ..

    Article Title: Manganese inhibits SVCV infection by promoting the expression of STING and the subsequent activation of IFN
    Article Snippet: Manganese (Mn) is necessary for various biological processes, yet its function in innate immunity has been less studied, especially in fish.. Stimulator of interferon (IFN) genes (STING) is an essential factor for IFN induction in virus infection.. Our study demonstrated that Mn2+ increases the ability of zebrafish to resist spring viraemia of carp virus (SVCV) infection by enhancing the expression of STING.

    Polymerase Chain Reaction:

    Article Title: Raffinose induces autophagy to promote plant growth
    Article Snippet: Finally, 200ng of total RNA was reverse transcribed with Superscript SentiFAST cDNA synthesis Kit (Bioline, London, UK). .. Real-time PCR reactions were performed in BIO-RAD HARD SHELL 96 well PCR Plates, using SYBR Green PCR Master Mix in the qRT-PCR (CFX Duet 96-well; Bio-Rad, Hercules, CA, USA). ..

    Article Title: Manganese inhibits SVCV infection by promoting the expression of STING and the subsequent activation of IFN
    Article Snippet: Manganese (Mn) is necessary for various biological processes, yet its function in innate immunity has been less studied, especially in fish.. Stimulator of interferon (IFN) genes (STING) is an essential factor for IFN induction in virus infection.. Our study demonstrated that Mn2+ increases the ability of zebrafish to resist spring viraemia of carp virus (SVCV) infection by enhancing the expression of STING.

    SYBR Green Assay:

    Article Title: Raffinose induces autophagy to promote plant growth
    Article Snippet: Finally, 200ng of total RNA was reverse transcribed with Superscript SentiFAST cDNA synthesis Kit (Bioline, London, UK). .. Real-time PCR reactions were performed in BIO-RAD HARD SHELL 96 well PCR Plates, using SYBR Green PCR Master Mix in the qRT-PCR (CFX Duet 96-well; Bio-Rad, Hercules, CA, USA). ..

    Article Title: Manganese inhibits SVCV infection by promoting the expression of STING and the subsequent activation of IFN
    Article Snippet: Manganese (Mn) is necessary for various biological processes, yet its function in innate immunity has been less studied, especially in fish.. Stimulator of interferon (IFN) genes (STING) is an essential factor for IFN induction in virus infection.. Our study demonstrated that Mn2+ increases the ability of zebrafish to resist spring viraemia of carp virus (SVCV) infection by enhancing the expression of STING.

    Quantitative RT-PCR:

    Article Title: Raffinose induces autophagy to promote plant growth
    Article Snippet: Finally, 200ng of total RNA was reverse transcribed with Superscript SentiFAST cDNA synthesis Kit (Bioline, London, UK). .. Real-time PCR reactions were performed in BIO-RAD HARD SHELL 96 well PCR Plates, using SYBR Green PCR Master Mix in the qRT-PCR (CFX Duet 96-well; Bio-Rad, Hercules, CA, USA). ..

    Synthesized:

    Article Title: Housing mice near vs. below thermoneutrality affects drug-induced weight loss but does not improve prediction of efficacy in humans
    Article Snippet: .. RNA was extracted using RNeasy Mini Kit (Cat. No. 74106, Qiagen, Hilden, Germany). cDNA was synthesized using iScript Reverse Transcription Supermix (Cat. No. 1708840, Bio-Rad Laboratories, inc. CA, USA) following manufacturer’s instructions. .. Gene expression was determined by quantitative real-time PCR on ViiA-7, using 1 ng of cDNA mixed with TaqMan OpenArray Real-Time PCR Master Mix (Applied Biosystems, Thermo Fisher Scientific, USA) and TaqMan probes listed in .

    Article Title: Manganese inhibits SVCV infection by promoting the expression of STING and the subsequent activation of IFN
    Article Snippet: Manganese (Mn) is necessary for various biological processes, yet its function in innate immunity has been less studied, especially in fish.. Stimulator of interferon (IFN) genes (STING) is an essential factor for IFN induction in virus infection.. Our study demonstrated that Mn2+ increases the ability of zebrafish to resist spring viraemia of carp virus (SVCV) infection by enhancing the expression of STING.

    Concentration Assay:

    Article Title: Tilorone mitigates the propagation of α-synucleinopathy in a midbrain-like organoid model
    Article Snippet: Total RNA was extracted from 10 brain organoid per each sample using TriPure reagent (Roche) and purified using RNeasy MinElute Cleanup Kit (Promega) following the standard protocols. .. The RNA concentration was measured by Nanodrop 2000 UV spectrophotometer, and 1 μg total RNA was converted to cDNA using the iScript Reverse Transcription Supermix (BioRad) system. ..

    Spectrophotometry:

    Article Title: Tilorone mitigates the propagation of α-synucleinopathy in a midbrain-like organoid model
    Article Snippet: Total RNA was extracted from 10 brain organoid per each sample using TriPure reagent (Roche) and purified using RNeasy MinElute Cleanup Kit (Promega) following the standard protocols. .. The RNA concentration was measured by Nanodrop 2000 UV spectrophotometer, and 1 μg total RNA was converted to cDNA using the iScript Reverse Transcription Supermix (BioRad) system. ..



    Similar Products

    99
    Bio-Rad iscript cdna synthesis supermix reverse transcriptase
    Iscript Cdna Synthesis Supermix Reverse Transcriptase, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/IScript+C+DNA+Synthesis+Kit/bio_rxiv__2025__05__08__652960-56-8-14
    Average 99 stars, based on 1 article reviews
    iscript cdna synthesis supermix reverse transcriptase - by Bioz Stars, 2026-11
    99/100 stars
      Buy from Supplier

    90
    Bio-Rad iscript reverse transcriptase supermix kit
    Iscript Reverse Transcriptase Supermix Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/iscript+reverse+transcription+supermix/pm37769118-78-46-52
    Average 90 stars, based on 1 article reviews
    iscript reverse transcriptase supermix kit - by Bioz Stars, 2026-11
    90/100 stars
      Buy from Supplier

    97
    Bio-Rad iscript reverse transcriptase supermix biorad 1708840 commercial assay
    Iscript Reverse Transcriptase Supermix Biorad 1708840 Commercial Assay, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/Bio-Rad+Protein+Assay+Kit+I/10__7554_slash_elife__74782-275-73-77
    Average 97 stars, based on 1 article reviews
    iscript reverse transcriptase supermix biorad 1708840 commercial assay - by Bioz Stars, 2026-11
    97/100 stars
      Buy from Supplier

    90
    Bio-Rad iscript reverse transcriptase supermix cdna rt-qpcr kit
    Loss of NK cell IFNAR1 impairs NK cell function, may impact adaptive immune regulation of tumorigenesis and increases lung metastasis. 1 × 105 EO771.LMB cells were injected into the fourth mammary fat pad (IMFP) of controliCre and Ifnar−/−NKp46 C57BL/6 mice at day 0 and subsequent alterations to circulating and primary tumor cells assessed. Peripheral blood (PB) was taken at day 7 for FACS analysis and for intracellular staining (ICS) of monocytes was performed at endpoint. a Primary tumor weights (mg) of control (n = 7) and Ifnar−/−NKp46 mice (n = 7) mice at experimental endpoint. Flow cytometric analysis of b absolute number (cell #) of primary tumor NK cells (n = 6/group). c PB CD69+ NK (NK1.1+) cell frequency (%). Primary tumor d CD69+ (e. representative plots shown) and f IFNγ+ NK cell frequency (%) and g IFNAR1 expression, represented as MFI (n = 5/group). Flow cytometric analysis of h CD8+ T cell IFNAR1 (MFI; n = 5/group) and i. PB CD69+ CD8+ T cells, j primary tumor CD69+ CD8+ T cells, k CD8+ IFNγ+ T cells, l. PB CD69+ CD4+ T cells and m primary tumor CD4+ IFNγ+ T cells, expressed as frequency (%). n <t>RT-qPCR</t> of mCherry (EO771.LMB) DNA expression in the lungs post-intravenous (IV) injection of EO771.LMB cells into WT (n = 9), controliCre (n = 5) and Ifnar−/−NKp46 (n = 8) mice at day 24. Representative fluorescence imaging of mCherry (EO771.LMB) in lungs shown for each group. All PB analysis (n = 7/group) and primary tumor analysis (n = 6/group). p values * < 0.05, ** < 0.005, *** < 0.0005. **** < 0.0001 determined by Student’s t test. Errors bars, SEM
    Iscript Reverse Transcriptase Supermix Cdna Rt Qpcr Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/iscript+reverse+transcriptase+supermix+cdna+rt+qpcr+kit/pmc10992771-85-26-28
    Average 90 stars, based on 1 article reviews
    iscript reverse transcriptase supermix cdna rt-qpcr kit - by Bioz Stars, 2026-11
    90/100 stars
      Buy from Supplier

    90
    Bio-Rad iscript reverse transcriptase supermix cdna for qrt–pcr kit (bio‐rad)
    A–C Bulk RNA‐seq analysis of DE genes (DEG) significantly suppressed (FDR < 0.05; generalized linear model extraction (GLM) by edgeR) in proliferating RM1 bone‐derived (BD) cells compared to parental RM1 and lung metastases. Tumor‐intrinsic type I IFN signaling is suppressed in proliferating bone lesions ( n = 1) compared to parental RM1 ( n = 2) cells as shown by (A) camera analysis of Hallmark gene set responses associated with bone metastasis (bar length is the –log 10 FDR, false discovery rate). Color indicates mean log 2 fold change (FC) of all genes in gene set. Bar width is relative gene set size. Dashed line shows FDR = 0.05; (B) barcode plot showing enrichment of the Hallmark IFN‐α response gene set in genes suppressed in bone metastases, using the signed log‐likelihood ratio statistic (EdgeR). Bars indicate value of the statistic for each gene in the gene set; (C) log 2 FC values of key downregulated IRGs, with genes retained in dormant cells and classical downstream IFN signaling targets indicated. Altered IRGs directly involved in IFN‐α/β production (light blue) compared to downstream IFN targets (dark blue) are segregated. P ‐values represented as * < 0.05, ** < .005, and *** < 0.0005; GLM by edgeR. D Schematic of proliferating RM1 cell isolation from bone and lung metastases following IC injection for preliminary RNA‐seq and orthogonal validation by <t>qRT–PCR.</t> E Heatmap of mean normalized voom expression of IRGs suppressed in RM1 bone metastases ( n = 1) compared to lung metastases ( n = 1) and parental cells ( n = 2). F qRT–PCR validation of Irf7 and Irf9 downregulation in RM1 cells from bone metastases (RMI BD) compared to parental RM1 cells, lung metastases (RM1 lung), and naïve bone marrow (BM) ( n = 3 mice per group). P ‐values represented as ** < 0.005, and *** < 0.0005 (Student's t ‐test). G qRT–PCR of Irf7 and Irf9 downregulation in parental RM1 cells and RM1 cells from bone metastases (RM1 BD) in WT and Ifnar1 ‐deficient (−/−) mice, with naïve BM from WT and Ifnar −/− animals for reference. ( n = 3 mice per group, n = 1 for Ifnar −/− BM control). P ‐values were represented as * < 0.05 and ** < 0.005 (Student's t ‐test). Data information: All error bars ± SEM. Source data are available online for this figure.
    Iscript Reverse Transcriptase Supermix Cdna For Qrt–Pcr Kit (Bio‐Rad), supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/CFX96+and+CFX384+Real-Time+PCR+Detection+Systems+Firmware+Update/pmc07271653-282-51-53
    Average 90 stars, based on 1 article reviews
    iscript reverse transcriptase supermix cdna for qrt–pcr kit (bio‐rad) - by Bioz Stars, 2026-11
    90/100 stars
      Buy from Supplier

    90
    Bio-Rad iscript supermix reverse transcriptase kit
    A–C Bulk RNA‐seq analysis of DE genes (DEG) significantly suppressed (FDR < 0.05; generalized linear model extraction (GLM) by edgeR) in proliferating RM1 bone‐derived (BD) cells compared to parental RM1 and lung metastases. Tumor‐intrinsic type I IFN signaling is suppressed in proliferating bone lesions ( n = 1) compared to parental RM1 ( n = 2) cells as shown by (A) camera analysis of Hallmark gene set responses associated with bone metastasis (bar length is the –log 10 FDR, false discovery rate). Color indicates mean log 2 fold change (FC) of all genes in gene set. Bar width is relative gene set size. Dashed line shows FDR = 0.05; (B) barcode plot showing enrichment of the Hallmark IFN‐α response gene set in genes suppressed in bone metastases, using the signed log‐likelihood ratio statistic (EdgeR). Bars indicate value of the statistic for each gene in the gene set; (C) log 2 FC values of key downregulated IRGs, with genes retained in dormant cells and classical downstream IFN signaling targets indicated. Altered IRGs directly involved in IFN‐α/β production (light blue) compared to downstream IFN targets (dark blue) are segregated. P ‐values represented as * < 0.05, ** < .005, and *** < 0.0005; GLM by edgeR. D Schematic of proliferating RM1 cell isolation from bone and lung metastases following IC injection for preliminary RNA‐seq and orthogonal validation by <t>qRT–PCR.</t> E Heatmap of mean normalized voom expression of IRGs suppressed in RM1 bone metastases ( n = 1) compared to lung metastases ( n = 1) and parental cells ( n = 2). F qRT–PCR validation of Irf7 and Irf9 downregulation in RM1 cells from bone metastases (RMI BD) compared to parental RM1 cells, lung metastases (RM1 lung), and naïve bone marrow (BM) ( n = 3 mice per group). P ‐values represented as ** < 0.005, and *** < 0.0005 (Student's t ‐test). G qRT–PCR of Irf7 and Irf9 downregulation in parental RM1 cells and RM1 cells from bone metastases (RM1 BD) in WT and Ifnar1 ‐deficient (−/−) mice, with naïve BM from WT and Ifnar −/− animals for reference. ( n = 3 mice per group, n = 1 for Ifnar −/− BM control). P ‐values were represented as * < 0.05 and ** < 0.005 (Student's t ‐test). Data information: All error bars ± SEM. Source data are available online for this figure.
    Iscript Supermix Reverse Transcriptase Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/iscript+supermix+reverse+transcriptase+kit/iscript+reverse+transcription+supermix/pmc04154239-111-28-33
    Average 90 stars, based on 1 article reviews
    iscript supermix reverse transcriptase kit - by Bioz Stars, 2026-11
    90/100 stars
      Buy from Supplier

    Image Search Results


    Loss of NK cell IFNAR1 impairs NK cell function, may impact adaptive immune regulation of tumorigenesis and increases lung metastasis. 1 × 105 EO771.LMB cells were injected into the fourth mammary fat pad (IMFP) of controliCre and Ifnar−/−NKp46 C57BL/6 mice at day 0 and subsequent alterations to circulating and primary tumor cells assessed. Peripheral blood (PB) was taken at day 7 for FACS analysis and for intracellular staining (ICS) of monocytes was performed at endpoint. a Primary tumor weights (mg) of control (n = 7) and Ifnar−/−NKp46 mice (n = 7) mice at experimental endpoint. Flow cytometric analysis of b absolute number (cell #) of primary tumor NK cells (n = 6/group). c PB CD69+ NK (NK1.1+) cell frequency (%). Primary tumor d CD69+ (e. representative plots shown) and f IFNγ+ NK cell frequency (%) and g IFNAR1 expression, represented as MFI (n = 5/group). Flow cytometric analysis of h CD8+ T cell IFNAR1 (MFI; n = 5/group) and i. PB CD69+ CD8+ T cells, j primary tumor CD69+ CD8+ T cells, k CD8+ IFNγ+ T cells, l. PB CD69+ CD4+ T cells and m primary tumor CD4+ IFNγ+ T cells, expressed as frequency (%). n RT-qPCR of mCherry (EO771.LMB) DNA expression in the lungs post-intravenous (IV) injection of EO771.LMB cells into WT (n = 9), controliCre (n = 5) and Ifnar−/−NKp46 (n = 8) mice at day 24. Representative fluorescence imaging of mCherry (EO771.LMB) in lungs shown for each group. All PB analysis (n = 7/group) and primary tumor analysis (n = 6/group). p values * < 0.05, ** < 0.005, *** < 0.0005. **** < 0.0001 determined by Student’s t test. Errors bars, SEM

    Journal: Cancer Immunology, Immunotherapy : CII

    Article Title: Loss of type I IFN responsiveness impairs natural killer cell antitumor activity in breast cancer

    doi: 10.1007/s00262-021-02857-z

    Figure Lengend Snippet: Loss of NK cell IFNAR1 impairs NK cell function, may impact adaptive immune regulation of tumorigenesis and increases lung metastasis. 1 × 105 EO771.LMB cells were injected into the fourth mammary fat pad (IMFP) of controliCre and Ifnar−/−NKp46 C57BL/6 mice at day 0 and subsequent alterations to circulating and primary tumor cells assessed. Peripheral blood (PB) was taken at day 7 for FACS analysis and for intracellular staining (ICS) of monocytes was performed at endpoint. a Primary tumor weights (mg) of control (n = 7) and Ifnar−/−NKp46 mice (n = 7) mice at experimental endpoint. Flow cytometric analysis of b absolute number (cell #) of primary tumor NK cells (n = 6/group). c PB CD69+ NK (NK1.1+) cell frequency (%). Primary tumor d CD69+ (e. representative plots shown) and f IFNγ+ NK cell frequency (%) and g IFNAR1 expression, represented as MFI (n = 5/group). Flow cytometric analysis of h CD8+ T cell IFNAR1 (MFI; n = 5/group) and i. PB CD69+ CD8+ T cells, j primary tumor CD69+ CD8+ T cells, k CD8+ IFNγ+ T cells, l. PB CD69+ CD4+ T cells and m primary tumor CD4+ IFNγ+ T cells, expressed as frequency (%). n RT-qPCR of mCherry (EO771.LMB) DNA expression in the lungs post-intravenous (IV) injection of EO771.LMB cells into WT (n = 9), controliCre (n = 5) and Ifnar−/−NKp46 (n = 8) mice at day 24. Representative fluorescence imaging of mCherry (EO771.LMB) in lungs shown for each group. All PB analysis (n = 7/group) and primary tumor analysis (n = 6/group). p values * < 0.05, ** < 0.005, *** < 0.0005. **** < 0.0001 determined by Student’s t test. Errors bars, SEM

    Article Snippet: When required, cells were transfected with poly I:C (10 μg/ml) overnight, prior to RNA extraction. cDNA was generated using the iScript Reverse Transcriptase Supermix cDNA for RT-qPCR kit (BioRad).

    Techniques: Cell Function Assay, Injection, Staining, Expressing, Quantitative RT-PCR, IV Injection, Fluorescence, Imaging

    A–C Bulk RNA‐seq analysis of DE genes (DEG) significantly suppressed (FDR < 0.05; generalized linear model extraction (GLM) by edgeR) in proliferating RM1 bone‐derived (BD) cells compared to parental RM1 and lung metastases. Tumor‐intrinsic type I IFN signaling is suppressed in proliferating bone lesions ( n = 1) compared to parental RM1 ( n = 2) cells as shown by (A) camera analysis of Hallmark gene set responses associated with bone metastasis (bar length is the –log 10 FDR, false discovery rate). Color indicates mean log 2 fold change (FC) of all genes in gene set. Bar width is relative gene set size. Dashed line shows FDR = 0.05; (B) barcode plot showing enrichment of the Hallmark IFN‐α response gene set in genes suppressed in bone metastases, using the signed log‐likelihood ratio statistic (EdgeR). Bars indicate value of the statistic for each gene in the gene set; (C) log 2 FC values of key downregulated IRGs, with genes retained in dormant cells and classical downstream IFN signaling targets indicated. Altered IRGs directly involved in IFN‐α/β production (light blue) compared to downstream IFN targets (dark blue) are segregated. P ‐values represented as * < 0.05, ** < .005, and *** < 0.0005; GLM by edgeR. D Schematic of proliferating RM1 cell isolation from bone and lung metastases following IC injection for preliminary RNA‐seq and orthogonal validation by qRT–PCR. E Heatmap of mean normalized voom expression of IRGs suppressed in RM1 bone metastases ( n = 1) compared to lung metastases ( n = 1) and parental cells ( n = 2). F qRT–PCR validation of Irf7 and Irf9 downregulation in RM1 cells from bone metastases (RMI BD) compared to parental RM1 cells, lung metastases (RM1 lung), and naïve bone marrow (BM) ( n = 3 mice per group). P ‐values represented as ** < 0.005, and *** < 0.0005 (Student's t ‐test). G qRT–PCR of Irf7 and Irf9 downregulation in parental RM1 cells and RM1 cells from bone metastases (RM1 BD) in WT and Ifnar1 ‐deficient (−/−) mice, with naïve BM from WT and Ifnar −/− animals for reference. ( n = 3 mice per group, n = 1 for Ifnar −/− BM control). P ‐values were represented as * < 0.05 and ** < 0.005 (Student's t ‐test). Data information: All error bars ± SEM. Source data are available online for this figure.

    Journal: EMBO Reports

    Article Title: Prostate cancer cell‐intrinsic interferon signaling regulates dormancy and metastatic outgrowth in bone

    doi: 10.15252/embr.202050162

    Figure Lengend Snippet: A–C Bulk RNA‐seq analysis of DE genes (DEG) significantly suppressed (FDR < 0.05; generalized linear model extraction (GLM) by edgeR) in proliferating RM1 bone‐derived (BD) cells compared to parental RM1 and lung metastases. Tumor‐intrinsic type I IFN signaling is suppressed in proliferating bone lesions ( n = 1) compared to parental RM1 ( n = 2) cells as shown by (A) camera analysis of Hallmark gene set responses associated with bone metastasis (bar length is the –log 10 FDR, false discovery rate). Color indicates mean log 2 fold change (FC) of all genes in gene set. Bar width is relative gene set size. Dashed line shows FDR = 0.05; (B) barcode plot showing enrichment of the Hallmark IFN‐α response gene set in genes suppressed in bone metastases, using the signed log‐likelihood ratio statistic (EdgeR). Bars indicate value of the statistic for each gene in the gene set; (C) log 2 FC values of key downregulated IRGs, with genes retained in dormant cells and classical downstream IFN signaling targets indicated. Altered IRGs directly involved in IFN‐α/β production (light blue) compared to downstream IFN targets (dark blue) are segregated. P ‐values represented as * < 0.05, ** < .005, and *** < 0.0005; GLM by edgeR. D Schematic of proliferating RM1 cell isolation from bone and lung metastases following IC injection for preliminary RNA‐seq and orthogonal validation by qRT–PCR. E Heatmap of mean normalized voom expression of IRGs suppressed in RM1 bone metastases ( n = 1) compared to lung metastases ( n = 1) and parental cells ( n = 2). F qRT–PCR validation of Irf7 and Irf9 downregulation in RM1 cells from bone metastases (RMI BD) compared to parental RM1 cells, lung metastases (RM1 lung), and naïve bone marrow (BM) ( n = 3 mice per group). P ‐values represented as ** < 0.005, and *** < 0.0005 (Student's t ‐test). G qRT–PCR of Irf7 and Irf9 downregulation in parental RM1 cells and RM1 cells from bone metastases (RM1 BD) in WT and Ifnar1 ‐deficient (−/−) mice, with naïve BM from WT and Ifnar −/− animals for reference. ( n = 3 mice per group, n = 1 for Ifnar −/− BM control). P ‐values were represented as * < 0.05 and ** < 0.005 (Student's t ‐test). Data information: All error bars ± SEM. Source data are available online for this figure.

    Article Snippet: When required, cells were transfected with poly I:C (10 μg/ml) overnight or treated with HDACi (entinostat [MS275], 1 μM [Selleckchem]; romidepsin [depsipeptide], 50 nM [Selleckchem]; or vorinostat [suberanilohydroxamic acid, SAHA], 2.5 μM [Selleckchem]) for 48 h prior to RNA extraction. cDNA was generated using the iScript Reverse Transcriptase Supermix cDNA for qRT–PCR kit (Bio‐Rad). qRT PCR was performed using SsoAdvanced Universal SYBR Green Supermix (Bio‐Rad) to quantify murine Irf7 , Irf9 , and Oas2 transcript expression on the CFX96 (Bio‐Rad) cycler per manufacturer's guidelines.

    Techniques: RNA Sequencing Assay, Derivative Assay, Cell Isolation, Injection, Quantitative RT-PCR, Expressing

    Stability of Irf7 and Irf9 mRNA suppression by qRT–PCR in ex vivo bone‐derived cells (RM1 BD Irf − , n = 7) in culture compared to a bone‐derived line that showed initial loss during early passage (RM1 BD REV (EP), n = 3), then reverted to parental expression levels at late passage (RM1 BD REV (LP), n = 4) compared to parental RM1 ( n = 3). ELISA of IFN‐α production by RM1 parental ( n = 3), RM1 bone‐derived Irf‐low (RM1 BD Irf − , n = 4), and RM1 BD REV ( n = 3) cells subsequent to poly I:C stimulation. qRT–PCR analysis of Irf7 and Irf9 expression in RM1 BD Irf − cells ± 48 h treatment with MS275 (1 μM) ( n = 7–9). Schematic of contact and transwell co‐culture systems. qRT–PCR analysis of Irf7 and Irf9 expression in parental RM1 cells ( n = 4) 48 h post‐contact culture with naïve BM ( n = 6). qRT–PCR analysis of Irf9 expression in parental RM1 cells ± 48 h co‐culture with naïve BM under contact (non‐transwell; NT) and transwell (0.4‐μm filters that prevent cell contact) conditions ( n = 6–8 per condition). qRT–PCR analysis of Irf9 expression in parental RM1 cells ± 48 h contact co‐culture with naïve BM ± MS275 (1 μM) ( n = 3–6 per condition). Data information: P ‐values represented as * < 0.05, ** < 0.005, and *** < 0.0005 (Student's t ‐test). All error bars ± SEM.

    Journal: EMBO Reports

    Article Title: Prostate cancer cell‐intrinsic interferon signaling regulates dormancy and metastatic outgrowth in bone

    doi: 10.15252/embr.202050162

    Figure Lengend Snippet: Stability of Irf7 and Irf9 mRNA suppression by qRT–PCR in ex vivo bone‐derived cells (RM1 BD Irf − , n = 7) in culture compared to a bone‐derived line that showed initial loss during early passage (RM1 BD REV (EP), n = 3), then reverted to parental expression levels at late passage (RM1 BD REV (LP), n = 4) compared to parental RM1 ( n = 3). ELISA of IFN‐α production by RM1 parental ( n = 3), RM1 bone‐derived Irf‐low (RM1 BD Irf − , n = 4), and RM1 BD REV ( n = 3) cells subsequent to poly I:C stimulation. qRT–PCR analysis of Irf7 and Irf9 expression in RM1 BD Irf − cells ± 48 h treatment with MS275 (1 μM) ( n = 7–9). Schematic of contact and transwell co‐culture systems. qRT–PCR analysis of Irf7 and Irf9 expression in parental RM1 cells ( n = 4) 48 h post‐contact culture with naïve BM ( n = 6). qRT–PCR analysis of Irf9 expression in parental RM1 cells ± 48 h co‐culture with naïve BM under contact (non‐transwell; NT) and transwell (0.4‐μm filters that prevent cell contact) conditions ( n = 6–8 per condition). qRT–PCR analysis of Irf9 expression in parental RM1 cells ± 48 h contact co‐culture with naïve BM ± MS275 (1 μM) ( n = 3–6 per condition). Data information: P ‐values represented as * < 0.05, ** < 0.005, and *** < 0.0005 (Student's t ‐test). All error bars ± SEM.

    Article Snippet: When required, cells were transfected with poly I:C (10 μg/ml) overnight or treated with HDACi (entinostat [MS275], 1 μM [Selleckchem]; romidepsin [depsipeptide], 50 nM [Selleckchem]; or vorinostat [suberanilohydroxamic acid, SAHA], 2.5 μM [Selleckchem]) for 48 h prior to RNA extraction. cDNA was generated using the iScript Reverse Transcriptase Supermix cDNA for qRT–PCR kit (Bio‐Rad). qRT PCR was performed using SsoAdvanced Universal SYBR Green Supermix (Bio‐Rad) to quantify murine Irf7 , Irf9 , and Oas2 transcript expression on the CFX96 (Bio‐Rad) cycler per manufacturer's guidelines.

    Techniques: Quantitative RT-PCR, Ex Vivo, Derivative Assay, Expressing, Enzyme-linked Immunosorbent Assay, Co-Culture Assay

    Assessment of tumor‐intrinsic IFN suppression stability over passage (P; number indicated) in culture by qRT–PCR analysis of mean Irf7 and Irf9 mRNA expression in bone‐derived RM1 Irf‐low (RM1 BD Irf − ) cells and a reverted (REV) bone‐derived cell line compared to RM1 parental cells. Values are means ± SEM of three independent experiments. HDACi impact on RM1 BD Irf − proliferation over time by SRB assay. Mean OD at 550 nm ( n = 3). Flow cytometry characterization of bone marrow lymphocyte (%) populations ( n = 3). qRT–PCR of Irf9 expression in parental RM1 cells 48, 72, and 96 h post‐contact co‐culture with FACS‐isolated naïve CD11b + Ly6G + BM cells ( n = 3 mice per time point). qRT–PCR of Irf7 expression in RM1 parental cells ± co‐culture with naïve BM ± 48 h treatment with MS275 ( n = 3–6). P ‐values represented as * < 0.05, ** < 0.005, and *** < 0.0005 (Student's t‐ test). All error bars ± SEM.

    Journal: EMBO Reports

    Article Title: Prostate cancer cell‐intrinsic interferon signaling regulates dormancy and metastatic outgrowth in bone

    doi: 10.15252/embr.202050162

    Figure Lengend Snippet: Assessment of tumor‐intrinsic IFN suppression stability over passage (P; number indicated) in culture by qRT–PCR analysis of mean Irf7 and Irf9 mRNA expression in bone‐derived RM1 Irf‐low (RM1 BD Irf − ) cells and a reverted (REV) bone‐derived cell line compared to RM1 parental cells. Values are means ± SEM of three independent experiments. HDACi impact on RM1 BD Irf − proliferation over time by SRB assay. Mean OD at 550 nm ( n = 3). Flow cytometry characterization of bone marrow lymphocyte (%) populations ( n = 3). qRT–PCR of Irf9 expression in parental RM1 cells 48, 72, and 96 h post‐contact co‐culture with FACS‐isolated naïve CD11b + Ly6G + BM cells ( n = 3 mice per time point). qRT–PCR of Irf7 expression in RM1 parental cells ± co‐culture with naïve BM ± 48 h treatment with MS275 ( n = 3–6). P ‐values represented as * < 0.05, ** < 0.005, and *** < 0.0005 (Student's t‐ test). All error bars ± SEM.

    Article Snippet: When required, cells were transfected with poly I:C (10 μg/ml) overnight or treated with HDACi (entinostat [MS275], 1 μM [Selleckchem]; romidepsin [depsipeptide], 50 nM [Selleckchem]; or vorinostat [suberanilohydroxamic acid, SAHA], 2.5 μM [Selleckchem]) for 48 h prior to RNA extraction. cDNA was generated using the iScript Reverse Transcriptase Supermix cDNA for qRT–PCR kit (Bio‐Rad). qRT PCR was performed using SsoAdvanced Universal SYBR Green Supermix (Bio‐Rad) to quantify murine Irf7 , Irf9 , and Oas2 transcript expression on the CFX96 (Bio‐Rad) cycler per manufacturer's guidelines.

    Techniques: Quantitative RT-PCR, Expressing, Derivative Assay, Sulforhodamine B Assay, Flow Cytometry, Co-Culture Assay, Isolation