2 × universal sybr green fast qpcr mix (MedChemExpress)
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2 × universal sybr green fast qpcr mix
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2 × Universal Sybr Green Fast Qpcr Mix, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 96/100, based on 123 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/universal+sybr+green+qpcr+master+mix/SYBR+Green+qPCR+Master+Mix/pmc13224022-35-0-8
Average 96 stars, based on 123 article reviews
2 × Universal Sybr Green Fast Qpcr Mix, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 96/100, based on 123 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/universal+sybr+green+qpcr+master+mix/SYBR+Green+qPCR+Master+Mix/pmc13224022-35-0-8
Average 96 stars, based on 123 article reviews
2 × universal sybr green fast qpcr mix - by Bioz Stars,
2026-09
96/100 stars
Images
1) Product Images from "CTSZ-dependent anoikis resistance enhances malignant characters of glioblastoma via NF-κB signaling"
Article Title: CTSZ-dependent anoikis resistance enhances malignant characters of glioblastoma via NF-κB signaling
Journal: iScience
doi: 10.1016/j.isci.2026.115992
Figure Legend Snippet:
Techniques Used: Immunohistochemistry, Virus, Recombinant, SYBR Green Assay, RNA Extraction, Bicinchoninic Acid Protein Assay, Viability Assay, Immunohistochemical staining, Double Staining, Real-time Polymerase Chain Reaction, shRNA, Cell Culture, Stable Transfection, Software
Related Articles
Quantitative RT-PCR:Article Title: Dynamic changes in genes and metabolites during embryonic development of Jiangshan black-bone chickens Article Snippet: cDNA was synthesized from total RNA using the PrimeScriptTM FAST RT Reagent Kit with gDNA Eraser (RR092A, Takara, China). .. Gene-specific primers, listed in , were designed via the NCBI Primer-BLAST tool, with GAPDH serving as the internal housekeeping gene for normalization. qRT-PCR was conducted on a QuantStudioTM 3 Real-Time PCR System (Applied Biosystems, USA) utilizing Article Title: Dynamic changes in genes and metabolites during embryonic development of Jiangshan black-bone chickens. Article Snippet: P < 0.05 indicates a significantly enriched profile. cDNA synthetized quantitative real-time PCR (qRT-PCR) analysis cDNA was synthesized from total RNA using the PrimeScriptTM FAST RT Reagent Kit with gDNA Eraser (RR092A, Takara, China). .. Genespecific primers, listed in Table S1, were designed via the NCBI Primer-BLAST tool, with GAPDH serving as the internal housekeeping gene for normalization. qRT-PCR was conducted on a QuantStudioTM 3 Real-Time PCR System (Applied Biosystems, USA) utilizing Real-time Polymerase Chain Reaction:Article Title: Dynamic changes in genes and metabolites during embryonic development of Jiangshan black-bone chickens Article Snippet: cDNA was synthesized from total RNA using the PrimeScriptTM FAST RT Reagent Kit with gDNA Eraser (RR092A, Takara, China). .. Gene-specific primers, listed in , were designed via the NCBI Primer-BLAST tool, with GAPDH serving as the internal housekeeping gene for normalization. qRT-PCR was conducted on a QuantStudioTM 3 Real-Time PCR System (Applied Biosystems, USA) utilizing Article Title: Dynamic changes in genes and metabolites during embryonic development of Jiangshan black-bone chickens. Article Snippet: P < 0.05 indicates a significantly enriched profile. cDNA synthetized quantitative real-time PCR (qRT-PCR) analysis cDNA was synthesized from total RNA using the PrimeScriptTM FAST RT Reagent Kit with gDNA Eraser (RR092A, Takara, China). .. Genespecific primers, listed in Table S1, were designed via the NCBI Primer-BLAST tool, with GAPDH serving as the internal housekeeping gene for normalization. qRT-PCR was conducted on a QuantStudioTM 3 Real-Time PCR System (Applied Biosystems, USA) utilizing Article Title: Multi-omics analysis reveals RBPJ-mediated regulation of EGF/ACTN2 / MYPN / COL21A1 in fibroblast during oviduct functional remodeling of duck Article Snippet: Gene-specific primers for qPCR were designed using the Primer-BLAST tool (National Center for Biotechnology Information, NCBI), with Beta-actin ( ACTB ) as the internal reference gene to normalize target gene expression. .. Primer sequences are listed in . qPCR was performed on a QuantStudio TM 3 Real-Time PCR System (applied biosystems, USA) using Article Title: Multi-Omics Analysis Reveals RBPJ-Mediated Regulation of EGF/ACTN2/MYPN/COL21A1 in Fibroblast during Oviduct Functional Remodeling of Duck Article Snippet: Gene-specific primers for qPCR were designed using the Primer-BLAST tool (National Center for Biotechnology Information, NCBI), with Beta-actin (ACTB) as the internal reference gene to normalize target gene expression. .. Primer sequences are listed in Table 1. qPCR was performed on a QuantStudioTM 3 Real-Time PCR System (applied biosystems, USA) using SYBR Green Assay:Article Title: Dynamic changes in genes and metabolites during embryonic development of Jiangshan black-bone chickens Article Snippet: cDNA was synthesized from total RNA using the PrimeScriptTM FAST RT Reagent Kit with gDNA Eraser (RR092A, Takara, China). .. Gene-specific primers, listed in , were designed via the NCBI Primer-BLAST tool, with GAPDH serving as the internal housekeeping gene for normalization. qRT-PCR was conducted on a QuantStudioTM 3 Real-Time PCR System (Applied Biosystems, USA) utilizing Article Title: Dynamic changes in genes and metabolites during embryonic development of Jiangshan black-bone chickens. Article Snippet: P < 0.05 indicates a significantly enriched profile. cDNA synthetized quantitative real-time PCR (qRT-PCR) analysis cDNA was synthesized from total RNA using the PrimeScriptTM FAST RT Reagent Kit with gDNA Eraser (RR092A, Takara, China). .. Genespecific primers, listed in Table S1, were designed via the NCBI Primer-BLAST tool, with GAPDH serving as the internal housekeeping gene for normalization. qRT-PCR was conducted on a QuantStudioTM 3 Real-Time PCR System (Applied Biosystems, USA) utilizing Article Title: Multi-omics analysis reveals RBPJ-mediated regulation of EGF/ACTN2 / MYPN / COL21A1 in fibroblast during oviduct functional remodeling of duck Article Snippet: Gene-specific primers for qPCR were designed using the Primer-BLAST tool (National Center for Biotechnology Information, NCBI), with Beta-actin ( ACTB ) as the internal reference gene to normalize target gene expression. .. Primer sequences are listed in . qPCR was performed on a QuantStudio TM 3 Real-Time PCR System (applied biosystems, USA) using Article Title: Multi-Omics Analysis Reveals RBPJ-Mediated Regulation of EGF/ACTN2/MYPN/COL21A1 in Fibroblast during Oviduct Functional Remodeling of Duck Article Snippet: Gene-specific primers for qPCR were designed using the Primer-BLAST tool (National Center for Biotechnology Information, NCBI), with Beta-actin (ACTB) as the internal reference gene to normalize target gene expression. .. Primer sequences are listed in Table 1. qPCR was performed on a QuantStudioTM 3 Real-Time PCR System (applied biosystems, USA) using |