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Keygen Biotech rna extraction utilized trizol
Rna Extraction Utilized Trizol, supplied by Keygen Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Related Articles

cDNA Synthesis:

Article Title: Comprehensive bioinformatic analysis and experimental validation identify MT1M and MT1X as key metallothioneins in BC pathogenesis.
Article Snippet: Background: Metallothioneins (MTs) are crucial metal-binding proteins involved in cellular zinc homeostasis and oxidative stress response.. However, the role of metallothionein-related genes (MRGs) in breast cancer (BC) pathogenesis and their potential as therapeutic targets remains poorly understood.. Methods: We integrated two BC datasets, GSE42568 and GSE29044, to identify differentially expressed MRGs.

Article Title: Remote Ischemic Preconditioning Enhances Skin Flap Survival via ZNF667/SDF1-Mediated Endothelial Progenitor Cells Functions for Angiogenesis.
Article Snippet: .. From both cells and tissues, the total RNA was extracted using TRIzol reagent (KeyGEN BioTECH, KGA1201, China) and further reversed to cDNA using the First-strand cDNA synthesis kit from KeyGen BioTECH (KGA1316). qPCR was conducted using Realtime PCR Master Mix (SYBR Green) from KeyGen BioTECH (KGA1339). ..

Real-time Polymerase Chain Reaction:

Article Title: Comprehensive bioinformatic analysis and experimental validation identify MT1M and MT1X as key metallothioneins in BC pathogenesis.
Article Snippet: Background: Metallothioneins (MTs) are crucial metal-binding proteins involved in cellular zinc homeostasis and oxidative stress response.. However, the role of metallothionein-related genes (MRGs) in breast cancer (BC) pathogenesis and their potential as therapeutic targets remains poorly understood.. Methods: We integrated two BC datasets, GSE42568 and GSE29044, to identify differentially expressed MRGs.

Article Title: Remote Ischemic Preconditioning Enhances Skin Flap Survival via ZNF667/SDF1-Mediated Endothelial Progenitor Cells Functions for Angiogenesis.
Article Snippet: .. From both cells and tissues, the total RNA was extracted using TRIzol reagent (KeyGEN BioTECH, KGA1201, China) and further reversed to cDNA using the First-strand cDNA synthesis kit from KeyGen BioTECH (KGA1316). qPCR was conducted using Realtime PCR Master Mix (SYBR Green) from KeyGen BioTECH (KGA1339). ..

Polymerase Chain Reaction:

Article Title: Comprehensive bioinformatic analysis and experimental validation identify MT1M and MT1X as key metallothioneins in BC pathogenesis.
Article Snippet: Background: Metallothioneins (MTs) are crucial metal-binding proteins involved in cellular zinc homeostasis and oxidative stress response.. However, the role of metallothionein-related genes (MRGs) in breast cancer (BC) pathogenesis and their potential as therapeutic targets remains poorly understood.. Methods: We integrated two BC datasets, GSE42568 and GSE29044, to identify differentially expressed MRGs.

Article Title: Remote Ischemic Preconditioning Enhances Skin Flap Survival via ZNF667/SDF1-Mediated Endothelial Progenitor Cells Functions for Angiogenesis.
Article Snippet: .. From both cells and tissues, the total RNA was extracted using TRIzol reagent (KeyGEN BioTECH, KGA1201, China) and further reversed to cDNA using the First-strand cDNA synthesis kit from KeyGen BioTECH (KGA1316). qPCR was conducted using Realtime PCR Master Mix (SYBR Green) from KeyGen BioTECH (KGA1339). ..

SYBR Green Assay:

Article Title: Comprehensive bioinformatic analysis and experimental validation identify MT1M and MT1X as key metallothioneins in BC pathogenesis.
Article Snippet: Background: Metallothioneins (MTs) are crucial metal-binding proteins involved in cellular zinc homeostasis and oxidative stress response.. However, the role of metallothionein-related genes (MRGs) in breast cancer (BC) pathogenesis and their potential as therapeutic targets remains poorly understood.. Methods: We integrated two BC datasets, GSE42568 and GSE29044, to identify differentially expressed MRGs.

Article Title: Remote Ischemic Preconditioning Enhances Skin Flap Survival via ZNF667/SDF1-Mediated Endothelial Progenitor Cells Functions for Angiogenesis.
Article Snippet: .. From both cells and tissues, the total RNA was extracted using TRIzol reagent (KeyGEN BioTECH, KGA1201, China) and further reversed to cDNA using the First-strand cDNA synthesis kit from KeyGen BioTECH (KGA1316). qPCR was conducted using Realtime PCR Master Mix (SYBR Green) from KeyGen BioTECH (KGA1339). ..

RNA Extraction:

Article Title: Label-Free Raman Spectroscopy Reveals Metabolic Signatures Associated with MGMT Promoter Methylation Status in Glioblastoma.
Article Snippet: Glioblastoma (GBM) response to Temozolomide (TMZ) critically depends on O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation.. Clinically, the unmethylated MGMT subtype�representing the predominant GBM population�universally develops TMZ resistance, driving an urgent need for novel therapeutics.. While metabolic reprogramming represents a potential therapeutic target, current methylation detection methods cannot provide targetable metabolic information.

Generated:

Article Title: Label-Free Raman Spectroscopy Reveals Metabolic Signatures Associated with MGMT Promoter Methylation Status in Glioblastoma.
Article Snippet: Glioblastoma (GBM) response to Temozolomide (TMZ) critically depends on O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation.. Clinically, the unmethylated MGMT subtype�representing the predominant GBM population�universally develops TMZ resistance, driving an urgent need for novel therapeutics.. While metabolic reprogramming represents a potential therapeutic target, current methylation detection methods cannot provide targetable metabolic information.

Quantitative RT-PCR:

Article Title: Label-Free Raman Spectroscopy Reveals Metabolic Signatures Associated with MGMT Promoter Methylation Status in Glioblastoma.
Article Snippet: Glioblastoma (GBM) response to Temozolomide (TMZ) critically depends on O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation.. Clinically, the unmethylated MGMT subtype�representing the predominant GBM population�universally develops TMZ resistance, driving an urgent need for novel therapeutics.. While metabolic reprogramming represents a potential therapeutic target, current methylation detection methods cannot provide targetable metabolic information.

CCK-8 Assay:

Article Title: Development of Stearic Acid Nanoemulsion for Therapeutic Delivery of Talazoparib Against Breast Cancer
Article Snippet: Hydrochloric acid (HCl), chloroform (CHCl3), and isopropanol (IPA, C3H8O) were purchased from Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China). .. DMEM, serum, CCK-8 reagent, Trizol reagent, DEPC water, and phosphate-buffered solution (PBS, 1×, pH 7.4) were purchased from KeyGEN Biotechnology Co. (Nanjing, China). .. Reverse transcription reagent HiScript III was purchased from Nanjing Novozymes Biotech Co., Ltd. (Vazyme R333-C1, Nanjing, China), and SYBR green master mix was purchased from BioEasy BSB113S1 (Hangzhou, China).

Concentration Assay:

Article Title: Development of Stearic Acid Nanoemulsion for Therapeutic Delivery of Talazoparib Against Breast Cancer
Article Snippet: .. Total RNA was extracted using Trizol reagent (KeyGEN BioTECH Co., China) according to the manufacturer’s protocol, and RNA concentration and purity were determined with a Porabio Pono-500 spectrophotometer. .. Complementary DNA (cDNA) was synthesized from 1 μg of total RNA using HiScript III reverse transcriptase (Vazyme, R333-C1, Nanjing, China).

Article Title: Development of Stearic Acid Nanoemulsion for Therapeutic Delivery of Talazoparib Against Breast Cancer
Article Snippet: .. Total RNA was extracted using Trizol reagent (KeyGEN BioTECH Co., China) according to the manufacturer’s protocol, and RNA concentration and purity were determined with a Porabio Pono-500 spectrophotometer. .. Complementary DNA (cDNA) was synthesized from 1 μg of total RNA using HiScript III reverse transcriptase (Vazyme, R333-C1, Nanjing, China).

Spectrophotometry:

Article Title: Development of Stearic Acid Nanoemulsion for Therapeutic Delivery of Talazoparib Against Breast Cancer
Article Snippet: .. Total RNA was extracted using Trizol reagent (KeyGEN BioTECH Co., China) according to the manufacturer’s protocol, and RNA concentration and purity were determined with a Porabio Pono-500 spectrophotometer. .. Complementary DNA (cDNA) was synthesized from 1 μg of total RNA using HiScript III reverse transcriptase (Vazyme, R333-C1, Nanjing, China).

Article Title: Development of Stearic Acid Nanoemulsion for Therapeutic Delivery of Talazoparib Against Breast Cancer
Article Snippet: .. Total RNA was extracted using Trizol reagent (KeyGEN BioTECH Co., China) according to the manufacturer’s protocol, and RNA concentration and purity were determined with a Porabio Pono-500 spectrophotometer. .. Complementary DNA (cDNA) was synthesized from 1 μg of total RNA using HiScript III reverse transcriptase (Vazyme, R333-C1, Nanjing, China).



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a was created by Figdraw. a , b Treatment schedule of the GL261 mouse brain tumor model (by figdraw.com). The detailed treatment sequence and time points. c , d Brain images of each group of mice obtained by T2 magnetic resonance imaging (MRI) with different treatments, where tumors are circled in white dashed lines. e-g Immunohistochemical images of tumor sections were examined at 15 days (Ki67 and PCNA, n = 5). h Survival curves of GBM tumor-bearing mice in different treatment groups ( n = 10). Survival analysis was calculated using the log-rank test. i Body weight changes of GBM tumor-bearing mice in different treatment groups ( n = 10). j , k Evaluation of antitumor effects of different treatments. n = 5 samples per group for data in ( c-f ) and ( i-k ). Data are expressed as the mean ± SD. Statistical significances were determined using one-way ANOVA with Fisher’s LSD post‑hoc test. Comparisons were performed between different groups in ( c-f ) and ( i-k ). Not significant (NS) is P ≥ 0.05, and significant P values are shown. n = 10 samples per group for data in ( h ). Survival analysis was compared using the log-rank test. Source data are provided as a file.

Journal: Nature Communications

Article Title: Low-intensity pulsed ultrasound-mediated nose-to-brain co-delivery of β-blockers and aPD-L1 enhances glioblastoma immunotherapy

doi: 10.1038/s41467-026-76103-4

Figure Lengend Snippet: a was created by Figdraw. a , b Treatment schedule of the GL261 mouse brain tumor model (by figdraw.com). The detailed treatment sequence and time points. c , d Brain images of each group of mice obtained by T2 magnetic resonance imaging (MRI) with different treatments, where tumors are circled in white dashed lines. e-g Immunohistochemical images of tumor sections were examined at 15 days (Ki67 and PCNA, n = 5). h Survival curves of GBM tumor-bearing mice in different treatment groups ( n = 10). Survival analysis was calculated using the log-rank test. i Body weight changes of GBM tumor-bearing mice in different treatment groups ( n = 10). j , k Evaluation of antitumor effects of different treatments. n = 5 samples per group for data in ( c-f ) and ( i-k ). Data are expressed as the mean ± SD. Statistical significances were determined using one-way ANOVA with Fisher’s LSD post‑hoc test. Comparisons were performed between different groups in ( c-f ) and ( i-k ). Not significant (NS) is P ≥ 0.05, and significant P values are shown. n = 10 samples per group for data in ( h ). Survival analysis was compared using the log-rank test. Source data are provided as a file.

Article Snippet: Immunohistochemical staining utilized PCNA (AC058, PCNA Mouse mAb, Abclonal) and Ki67 (A26755PM, Ki67 Rabbit PolymAb®, Abclonal) antibodies, with technical assistance from Nanjing Youmeng Biotechnology Co., Ltd. Tumor sections underwent immunofluorescence staining using a TUNEL assay kit (Beyotime Biotech, Shanghai, China).

Techniques: Sequencing, Magnetic Resonance Imaging, Immunohistochemical staining