Liquid probe-based one-step RT-qPCR formulation with reverse transcriptase and DNA amplification reagents. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid probe-based one-step RT-qPCR formulation with reverse transcriptase and DNA amplification reagents. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid master mix for probe-based DNA qPCR. Check instrument reference-dye requirements and multiplex compatibility. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid master mix for probe-based DNA qPCR. Check instrument reference-dye requirements and multiplex compatibility. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid master mix for probe-based DNA qPCR. Check instrument reference-dye requirements and multiplex compatibility. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid intercalating-dye master mix for DNA qPCR; ROX and tracer-dye formulations differ. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid intercalating-dye master mix for DNA qPCR; ROX and tracer-dye formulations differ. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid master mix for probe-based DNA qPCR. Check instrument reference-dye requirements and multiplex compatibility. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Liquid master mix for probe-based DNA qPCR. Check instrument reference-dye requirements and multiplex compatibility. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Mild nonionic-detergent bacterial lysis reagent in Tris buffer. Does not itself contain enzymes; validate extraction efficiency and add lysozyme or nuclease when needed.
Microbial DNA extraction / Spin-column purification
Spin-column bacterial genomic DNA purification after zirconia/ceramic bead-beating lysis. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Microbial DNA extraction / Spin-column purification
Spin-column genomic DNA purification from Gram-positive and Gram-negative bacteria. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Microbial DNA extraction / Spin-column purification
Glass-fiber spin columns extract genomic DNA from Gram-positive and Gram-negative bacteria. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Spin-column bacterial total RNA extraction with lysozyme-assisted lysis and DNase. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Spin-column bacterial total RNA extraction with lysozyme-assisted lysis, without DNase. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Candidate category only. Match the stated sample, material, capacity, geometry and required output before comparison; experimental interchangeability is not established.
Microbial DNA extraction / Spin-column purification
Spin-column genomic DNA isolation from Gram-positive and Gram-negative bacteria. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Manufacturer catalog identifies the named restriction enzyme and catalog code. Isoschizomer aliases are not treated as interchangeable products; check cleavage position, methylation sensitivity, temperature and buffer. Confirm the supplier protocol, formulation and activity units before substitution.