Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
Requires review: exact composition, calibration, formulation, kit or hardware compatibility, or regulatory identity is not fully established by the captured manufacturer description. Shared function is insufficient for substitution.
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. ATP solid reagent; prepare concentration and pH required by protocol.
Spin-column yeast and fungal total RNA extraction with bead-beating lysis. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.
Cell-impermeant benzylguanine substrate for labeling surface-exposed SNAP-tag proteins. AF488 excitation/emission maxima are 495/519 nm; compare spectral behavior with the intended 488-channel substrate.
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.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.
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.
Official manufacturer catalog lists this exact named enzyme and catalog code with a product-page hyperlink. Product-page body was unavailable due to a locale redirect; verify detailed conditions with the supplier. Confirm the supplier protocol, formulation and activity units before substitution.
Silica-membrane spin-column agarose gel DNA recovery for fragments from 100 bp to 10 kb. Candidate for the specified application; follow the manufacturer protocol and validate sample and instrument compatibility.