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Sangon Biotech dna loading buffer
Dna Loading Buffer, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dna+loading+buffer/buffer+lysis+ripa/pm41871234-43-5-20
Average 86 stars, based on 1 article reviews
dna loading buffer - by Bioz Stars, 2026-09
86/100 stars

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Related Articles

Marker:

Article Title: Dz-SiG CRISPR: A DNAzyme-Switched G-quadruplex-lock CRISPR system for isothermal and rapid detection of lead ions.
Article Snippet: Lead (Pb2+) poses serious risks to health and ecosystems, necessitating rapid, ultrasensitive detection.. CRISPR/ Cas12a systems offers exceptional specificity and intrinsic signal amplification.. Nevertheless, their adaptation to Pb2+ is hindered by the lack of programmable interfaces to convert small-molecule binding into Cas12a activation.

Article Title: Rapid On-Site Detection of Pseudomonas aeruginosa via ecfX-Targeted Loop-Mediated Isothermal Amplification
Article Snippet: Bst II Pro DNA Polymerase Large Fragment (P703-01, Vazyme, Nanjing, China), dNTPs and LAMP Fluorescent Dye (New England Biolabs, Ipswich, MA, USA) were employed for the LAMP assay. .. Goldview Nucleic Acid Gel Stain (10,000×, Yeasen Biotechnology, Shanghai, China), agarose, 6× DNA loading buffer, DNA marker (100–600 bp), ddH 2 O, 50× TAE buffer, and primers were purchased from Sangon Biotech. ..

Article Title: Tetrahedral DNA cluster-based signal-amplified Impedimetric biosensor for ultrasensitive detection of Ochratoxin A
Article Snippet: Ochratoxin A (OTA) is a highly toxic mycotoxin with nepHrotoxicity, hepatotoxicity, and carcinogenicity.. It poses a long-term threat to the health of humans and animals.. Although screen printed electrodes (SPE) with aptamer functionalization provide promising detection capabilities, their applications are limited by inherent weak electrochemical signals, prompting the need for signal amplification strategies.

Article Title: One-Pot CRISPR/Cas12a Assay Based on Ultrashort HDA for Ultrasensitive and Universal Nucleic Acid Detection.
Article Snippet: Isothermal amplification techniques, such as helicase-dependent amplification (HDA) combined with CRISPR, are cutting-edge approaches for nucleic acid detection.. In this work, we developed a novel ultrashort mesophilic HDA (termed usHDA) for rapid, highly sensitive nucleic acid amplification at 37 °C and constructed a one-pot usHDA-CRISPR/Cas12 assay.. The usHDA is specifically designed for rapid amplification of ultrashort sequences (about 40 nt) at 37 °C within 30 min.

Article Title: Tandem Repeat Generation and Novel Isothermal Amplification Based on Nonspecific Tailing and Replication Slippage.
Article Snippet: .. DNA oligonucleotide, polyacrylamide, dNTP mixture, DNA marker, acrylamide/bisacrylamide solution, ethidium bromide, and 6× DNA loading buffer were purchased from Shanghai Sangon Biotech. .. Bst 3.0, 10× Isothermal Amplification Buffer, and 100 mM magnesium sulfate were purchased from New England Biolabs.

Staining:

Article Title: Rapid On-Site Detection of Pseudomonas aeruginosa via ecfX-Targeted Loop-Mediated Isothermal Amplification
Article Snippet: Bst II Pro DNA Polymerase Large Fragment (P703-01, Vazyme, Nanjing, China), dNTPs and LAMP Fluorescent Dye (New England Biolabs, Ipswich, MA, USA) were employed for the LAMP assay. .. Goldview Nucleic Acid Gel Stain (10,000×, Yeasen Biotechnology, Shanghai, China), agarose, 6× DNA loading buffer, DNA marker (100–600 bp), ddH 2 O, 50× TAE buffer, and primers were purchased from Sangon Biotech. ..

Article Title: Hierarchical Hybridization Chain Reaction for Amplified Signal Output and Cascade DNA Logic Circuits.
Article Snippet: In this work, we propose a three-layer hierarchical hybridization chain reaction (3L hHCR) composed of HCR, HCR, and HCR to achieve robust signal amplification efficiency and broaden the applied range of HCR-based systems.. In principle, the execution of superior HCR generates the formation of the initiator (named as I or I) of the subordinate HCR that relies on the introduction of the target sequence (I).. To avoid the high background signal of the 3L hHCR system, a strategy of “splitting reconstruction” was adopted.

Article Title: 3, 4-Dihydroxy-l-phenylalanine Biopolymer Cellulose DNA Adhesive Card as an Enhanced Solid-Phase One-Step DNA Extraction Method from Foodborne Pathogens in Food Samples
Article Snippet: Deoxyribonucleic acid (DNA) extraction, which is the mainstay of molecular amplification for food pathogen detection procedure, is dependent on laboratory infrastructure, cumbersome methods, and time consumption.. To tackle these dependencies, we developed an enhanced mussel-inspired cellulose card for the convenient, eco-friendly, and rapid DNA extraction from bacteria present in food.. This enhanced cellulose mussel-inspired DNA adhesive card (BDA card) was successfully prepared using Na + through the self-polymerization of biopolymer polyvalent ions and 3,4-dihydroxy-l-phenylalanine (L-Dopa).

High Performance Liquid Chromatography:

Article Title: Hierarchical Hybridization Chain Reaction for Amplified Signal Output and Cascade DNA Logic Circuits.
Article Snippet: In this work, we propose a three-layer hierarchical hybridization chain reaction (3L hHCR) composed of HCR, HCR, and HCR to achieve robust signal amplification efficiency and broaden the applied range of HCR-based systems.. In principle, the execution of superior HCR generates the formation of the initiator (named as I or I) of the subordinate HCR that relies on the introduction of the target sequence (I).. To avoid the high background signal of the 3L hHCR system, a strategy of “splitting reconstruction” was adopted.

Sequencing:

Article Title: Hierarchical Hybridization Chain Reaction for Amplified Signal Output and Cascade DNA Logic Circuits.
Article Snippet: In this work, we propose a three-layer hierarchical hybridization chain reaction (3L hHCR) composed of HCR, HCR, and HCR to achieve robust signal amplification efficiency and broaden the applied range of HCR-based systems.. In principle, the execution of superior HCR generates the formation of the initiator (named as I or I) of the subordinate HCR that relies on the introduction of the target sequence (I).. To avoid the high background signal of the 3L hHCR system, a strategy of “splitting reconstruction” was adopted.

Polymerase Chain Reaction:

Article Title: 3, 4-Dihydroxy-l-phenylalanine Biopolymer Cellulose DNA Adhesive Card as an Enhanced Solid-Phase One-Step DNA Extraction Method from Foodborne Pathogens in Food Samples
Article Snippet: Deoxyribonucleic acid (DNA) extraction, which is the mainstay of molecular amplification for food pathogen detection procedure, is dependent on laboratory infrastructure, cumbersome methods, and time consumption.. To tackle these dependencies, we developed an enhanced mussel-inspired cellulose card for the convenient, eco-friendly, and rapid DNA extraction from bacteria present in food.. This enhanced cellulose mussel-inspired DNA adhesive card (BDA card) was successfully prepared using Na + through the self-polymerization of biopolymer polyvalent ions and 3,4-dihydroxy-l-phenylalanine (L-Dopa).

Electrophoresis:

Article Title: 3, 4-Dihydroxy-l-phenylalanine Biopolymer Cellulose DNA Adhesive Card as an Enhanced Solid-Phase One-Step DNA Extraction Method from Foodborne Pathogens in Food Samples
Article Snippet: Deoxyribonucleic acid (DNA) extraction, which is the mainstay of molecular amplification for food pathogen detection procedure, is dependent on laboratory infrastructure, cumbersome methods, and time consumption.. To tackle these dependencies, we developed an enhanced mussel-inspired cellulose card for the convenient, eco-friendly, and rapid DNA extraction from bacteria present in food.. This enhanced cellulose mussel-inspired DNA adhesive card (BDA card) was successfully prepared using Na + through the self-polymerization of biopolymer polyvalent ions and 3,4-dihydroxy-l-phenylalanine (L-Dopa).

Bacteria:

Article Title: 3, 4-Dihydroxy-l-phenylalanine Biopolymer Cellulose DNA Adhesive Card as an Enhanced Solid-Phase One-Step DNA Extraction Method from Foodborne Pathogens in Food Samples
Article Snippet: Deoxyribonucleic acid (DNA) extraction, which is the mainstay of molecular amplification for food pathogen detection procedure, is dependent on laboratory infrastructure, cumbersome methods, and time consumption.. To tackle these dependencies, we developed an enhanced mussel-inspired cellulose card for the convenient, eco-friendly, and rapid DNA extraction from bacteria present in food.. This enhanced cellulose mussel-inspired DNA adhesive card (BDA card) was successfully prepared using Na + through the self-polymerization of biopolymer polyvalent ions and 3,4-dihydroxy-l-phenylalanine (L-Dopa).

DNA Purification:

Article Title: 3, 4-Dihydroxy-l-phenylalanine Biopolymer Cellulose DNA Adhesive Card as an Enhanced Solid-Phase One-Step DNA Extraction Method from Foodborne Pathogens in Food Samples
Article Snippet: Deoxyribonucleic acid (DNA) extraction, which is the mainstay of molecular amplification for food pathogen detection procedure, is dependent on laboratory infrastructure, cumbersome methods, and time consumption.. To tackle these dependencies, we developed an enhanced mussel-inspired cellulose card for the convenient, eco-friendly, and rapid DNA extraction from bacteria present in food.. This enhanced cellulose mussel-inspired DNA adhesive card (BDA card) was successfully prepared using Na + through the self-polymerization of biopolymer polyvalent ions and 3,4-dihydroxy-l-phenylalanine (L-Dopa).

Stripping Membranes:

Article Title: 3, 4-Dihydroxy-l-phenylalanine Biopolymer Cellulose DNA Adhesive Card as an Enhanced Solid-Phase One-Step DNA Extraction Method from Foodborne Pathogens in Food Samples
Article Snippet: Deoxyribonucleic acid (DNA) extraction, which is the mainstay of molecular amplification for food pathogen detection procedure, is dependent on laboratory infrastructure, cumbersome methods, and time consumption.. To tackle these dependencies, we developed an enhanced mussel-inspired cellulose card for the convenient, eco-friendly, and rapid DNA extraction from bacteria present in food.. This enhanced cellulose mussel-inspired DNA adhesive card (BDA card) was successfully prepared using Na + through the self-polymerization of biopolymer polyvalent ions and 3,4-dihydroxy-l-phenylalanine (L-Dopa).



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