In vitro protein synthesis / E. coli lysate continuous-exchange disulfide-protein systems
RTS 500 continuous-exchange E. coli lysate system for disulfide-containing proteins; use its dedicated reaction device. Review the manufacturer protocol before substituting.
In vitro protein synthesis / E. coli lysate continuous-exchange translation systems
E. coli lysate translation kit using an RTS 500 continuous-exchange device and plasmid templates. Review the manufacturer protocol before substituting.
In vitro protein synthesis / Wheat germ continuous-exchange translation systems
RTS 500 wheat germ lysate translation system using continuous exchange; scale and device differ from RTS 100. Review the manufacturer protocol before substituting.
In vitro protein synthesis / E. coli lysate continuous-exchange translation systems
E. coli lysate translation kit using an RTS 9000 continuous-exchange device; different scale from RTS 500. Review the manufacturer protocol before substituting.
DnaK, DnaJ and GrpE chaperone supplement for cell-free protein expression; distinct from GroEL/GroES. Review the manufacturer protocol before substituting.
Hot-start endpoint PCR master mix includes red dye and gel loading buffer. Candidate for the listed workflow; compare buffer, sample input and protocol requirements before substitution.
Standard PCR / Master mixes / Ready-to-load PCR mixes
Standard Taq PCR master mix includes red dye and density components for direct gel loading. Candidate for the listed workflow; compare buffer, sample input and protocol requirements 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.
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.
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.
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.
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.
In vitro protein synthesis / E. coli lysate-based translation systems
Candidate only. Verify activity, specificity, formulation and protocol compatibility before substitution. E. coli extract cell-free protein synthesis driven by T7 transcription.
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.
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.
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.
Same enzyme identity candidate. Verify recognition and cleavage specificity, methylation sensitivity, reaction buffer, concentration and heat inactivation in the source before substitution.