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Glycan modification enzymes / Sialidases / alpha 2-3,6,8 Neuraminidase
Terminal sialic acid cleavage at alpha2-3, alpha2-6 and alpha2-8 linkages. Confirm substrate accessibility and activity requirements.
Collection and elution plates / 96-well plates / 200 microliter V-bottom wells
Polystyrene material: confirm centrifugation, solvent and receiver-plate compatibility. Polystyrene plate material and receiver geometry may differ from Zymo elution plates.
Purification plates / 96-well silica plates / 5 micrograms DNA or RNA per well
Geometry and binding attributes are documented where available, but compatible buffers, fragment recovery and processor fit require verification before substitution.
Purification plates / 96-well inhibitor-removal plates
Geometry and binding attributes are documented where available, but compatible buffers, fragment recovery and processor fit require verification before substitution.
Chromatin immunoprecipitation
Agarose bead format; antibody compatibility, fragmentation and sample requirements differ.
Self-labeling tags & substrates / SNAP-tag reagents / Intracellular labeling substrates / 647SiR
Cell-permeable benzylguanine SiR substrate for SNAP-tag labeling. Manufacturer states chemical identity with SNAP-Cell 647-SiR; confirm optical filters and labeling conditions.
RNA ladders / Double-stranded RNA ladders
Ten double-stranded RNA fragments of 20, 30, 40, 50, 100, 200, 300, 400, 500 and 1000 bp. Loading buffer is supplied separately.
PCR cleanup / Magnetic bead purification
SPRI magnetic beads purify DNA and support size selection by changing bead ratio. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
SmaI restriction enzymes / Standard formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
SmaI restriction enzymes / Standard formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
SmaI restriction enzymes / Standard formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
SmaI restriction enzymes / Standard formulations
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.
SmaI restriction enzymes / Standard formulations
Official product page specifies the named restriction enzyme and catalog number. Classified as a standard formulation; verify recognition sequence, methylation sensitivity, temperature and recommended buffer. Confirm formulation, activity units and experimental conditions before substitution.
SmaI restriction enzymes / Fast-digest formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
SmaI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
Gel extraction / Spin-column purification
Spin-column cleanup of 40-200 bp DNA fragments from gels or PCR; manufacturer reports 10 µg capacity. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
RNA library preparation / Small RNA library preparation
Small RNA library preparation for Illumina sequencing using RNA adapter ligation and reverse transcription. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Reverse transcriptase enzymes / Engineered reverse transcriptases
Engineered reverse transcriptase with reduced RNase H activity and increased thermal stability. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Two-step RT-PCR kits
Two-step kit combining first-strand cDNA synthesis and a separate endpoint PCR stage. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
Immune repertoire sequencing
Catalog category candidate. Experimental interchangeability has not been validated.
Template-switching RT
Engineered MMLV reverse transcriptase with terminal-transferase activity and a documented template-switching protocol for full-length cDNA. Candidate for this workflow; confirm formulation, substrate and protocol compatibility before substitution.
SmiI restriction enzymes / Standard formulations
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.
SmiI restriction enzymes / Fast-digest formulations
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
SmlI restriction enzymes / Standard formulations
Classification is based on the supplied product name. Confirm formulation, application and compatibility in the manufacturer documentation.
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